0001387131-15-003188.txt : 20151109 0001387131-15-003188.hdr.sgml : 20151109 20151105161549 ACCESSION NUMBER: 0001387131-15-003188 CONFORMED SUBMISSION TYPE: 10-Q PUBLIC DOCUMENT COUNT: 11 CONFORMED PERIOD OF REPORT: 20150930 FILED AS OF DATE: 20151105 DATE AS OF CHANGE: 20151105 FILER: COMPANY DATA: COMPANY CONFORMED NAME: TherapeuticsMD, Inc. CENTRAL INDEX KEY: 0000025743 STANDARD INDUSTRIAL CLASSIFICATION: PHARMACEUTICAL PREPARATIONS [2834] IRS NUMBER: 870233535 STATE OF INCORPORATION: NV FISCAL YEAR END: 1231 FILING VALUES: FORM TYPE: 10-Q SEC ACT: 1934 Act SEC FILE NUMBER: 001-00100 FILM NUMBER: 151200838 BUSINESS ADDRESS: STREET 1: 6800 BROKEN SOUND PARKWAY NW STREET 2: THIRD FLOOR CITY: BOCA RATON STATE: FL ZIP: 33487 BUSINESS PHONE: 561-961-1911 MAIL ADDRESS: STREET 1: 6800 BROKEN SOUND PARKWAY NW STREET 2: THIRD FLOOR CITY: BOCA RATON STATE: FL ZIP: 33487 FORMER COMPANY: FORMER CONFORMED NAME: AMHN, Inc. DATE OF NAME CHANGE: 20090930 FORMER COMPANY: FORMER CONFORMED NAME: CROFF ENTERPRISES INC DATE OF NAME CHANGE: 19970915 FORMER COMPANY: FORMER CONFORMED NAME: CROFF OIL CO DATE OF NAME CHANGE: 19920703 10-Q 1 txmd-10q_093015.htm QUARTERLY REPORT

 

 

 

UNITED STATES 

SECURITIES AND EXCHANGE COMMISSION

WASHINGTON, D.C. 20549

 

FORM 10-Q

 

(Mark One)

QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934

 

For the quarterly period ended September 30, 2015

 

 ☐ TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934

 

For the transition period from________ to ___________

 

Commission File No. 001-00100

 

THERAPEUTICSMD, INC. 

(Exact Name of Registrant as Specified in Its Charter)

 

Nevada   87-0233535
(State or Other Jurisdiction of Incorporation or Organization)   (I.R.S. Employer Identification No.)
     
6800 Broken Sound Parkway NW, Third Floor, Boca Raton, FL 33487   (561) 961-1900
(Address of Principal Executive Offices)   (Issuer’s Telephone Number)

 

N/A

(Former Name, Former Address and Former Fiscal Year, if Changed Since Last Report)

 

Indicate by check mark whether the registrant: (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such filing requirements for the past 90 days.   Yes  ☒    No  ☐

 

Indicate by check mark whether the registrant has submitted electronically and posted on its corporate Web site, if any, every Interactive Data File required to be submitted and posted pursuant to Rule 405 of Regulation S-T (§232.405 of this chapter) during the preceding 12 months (or for such shorter period that the registrant was required to submit and post such files).   Yes  ☒    No  ☐

 

Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, or a smaller reporting company. See the definitions of “large accelerated filer,” “accelerated filer” and “smaller reporting company” in Rule 12b-2 of the Exchange Act (Check one):

 

Large accelerated filer  ☐   Accelerated filer  ☒
Non-accelerated filer  ☐   Smaller reporting company  ☐
(Do not check if a smaller reporting company)    

 

Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Exchange Act).   Yes  ☐    No  ☒

 

The number of shares outstanding of the registrant’s common stock, par value $0.001 per share, as of November 2, 2015 was 177,848,041.

 

 

 

 
 

 

 

THERAPEUTICSMD, INC. AND SUBSIDIARIES
INDEX
         
        Page
PART I - FINANCIAL INFORMATION    
         
  Item 1. Financial Statements    
         
    Consolidated Balance Sheets as of September 30, 2015 (Unaudited) and December 31, 2014   3
         
    Consolidated Statements of Operations for the Three and Nine Months Ended September 30, 2015 (Unaudited) and 2014 (Unaudited)   4
         
    Consolidated Statements of Cash Flows for the Nine Months Ended September 30, 2015 (Unaudited) and 2014 (Unaudited)   5
         
    Notes to Consolidated Financial Statements (Unaudited)   6
         
  Item 2. Management's Discussion and Analysis of Financial Condition and Results of Operations   19
         
  Item 3. Quantitative and Qualitative Disclosures about Market Risk   30
         
  Item 4. Controls and Procedures   31
         
Part II - OTHER INFORMATION   31
         
  Item 1. Legal Proceedings   31
         
  Item 1A. Risk Factors   31
         
  Item 2. Unregistered Sales of Equity Securities and Use of Proceeds   32
         
  Item 6. Exhibits   32
         
Signatures     33

 

 

 

2 
 

 PART I - FINANCIAL INFORMATION

 Item 1.  Financial Statements

 

 
THERAPEUTICSMD, INC. AND SUBSIDIARIES
CONSOLIDATED BALANCE SHEETS

 
    September 30, 2015   December 31, 2014
    (Unaudited)    
         
ASSETS
Current Assets:                
Cash   $ 81,123,988     $ 51,361,607  
Accounts receivable, net of allowance for doubtful accounts                
  of $96,916 and $59,753, respectively     3,666,586       2,154,217  
Inventory     870,059       1,182,113  
Other current assets                    2,120,805       1,537,407  
     Total current assets     87,781,438       56,235,344  
                 
Fixed assets, net     56,748       63,293  
                 
Other Assets:                
Prepaid expense     1,172,051       1,427,263  
Intangible assets, net                    1,324,284       1,228,588  
Security deposit     125,000       125,000  
     Total other assets     2,621,335       2,780,851  
       Total assets   $ 90,459,521     $ 59,079,488  
                 
 LIABILITIES AND STOCKHOLDERS' EQUITY                
Current Liabilities:                
Accounts payable   $ 5,301,625     $ 6,327,129  
Other current liabilities     6,386,777       3,840,639  
Deferred revenue     —         522,613  
     Total current liabilities     11,688,402       10,690,381  
                 
Long-Term Liabilities:                
Accrued expenses     1,213,874       —    
       Total liabilities     12,902,276       10,690,381  
                 
Commitments and Contingencies - See Note 15                
                 
Stockholders' Equity:                
Preferred stock - par value $0.001; 10,000,000 shares authorized;                
  no shares issued and outstanding     —         —    
Common stock - par value $0.001; 350,000,000 and 250,000,000 shares                
 authorized;  177,787,927 and 156,097,019 issued and outstanding, respectively     177,788       156,097  
Additional paid-in capital     279,723,640       182,982,846  
Accumulated deficit     (202,344,183 )     (134,749,836 )
     Total stockholders' equity     77,557,245       48,389,107  
       Total liabilities and stockholders' equity   $ 90,459,521     $ 59,079,488  

 

 

The accompanying footnotes are an integral part of these consolidated financial statements.

 

3 
 

THERAPEUTICSMD, INC. AND SUBSIDIARIES
CONSOLIDATED STATEMENTS OF OPERATIONS

 

    Three Months Ended   Nine Months Ended
    September 30,   September 30
    2015   2014   2015   2014
    (Unaudited)   (Unaudited)   (Unaudited)   (Unaudited)
                 
Revenues, net   $ 5,190,175     $ 4,186,261     $ 14,513,158     $ 10,768,572  
                                 
Cost of goods sold     1,193,965       1,068,605       3,270,695       2,792,268  
                                 
Gross profit     3,996,210       3,117,656       11,242,463       7,976,304  
                                 
Operating expenses:                                
Sales, general, and administration     7,060,944       6,043,354       20,089,998       16,610,015  
Research and development     16,421,753       14,909,430       58,789,302       29,052,149  
Depreciation and amortization     16,548       12,747       44,400       39,909  
     Total operating expenses     23,499,245       20,965,531       78,923,700       45,702,073  
                                 
Operating loss     (19,503,035 )     (17,847,875 )     (67,681,237 )     (37,725,769 )
                                 
Other income (expense):                                
Miscellaneous income     27,630       6,260       71,728       43,411  
Interest income     2,760       9,364       15,162       27,756  
Financing costs     —         —         —         (260,027 )
     Total other income (expense)     30,390       15,624       86,890       (188,860 )
                                 
Loss before income taxes     (19,472,645 )     (17,832,251 )     (67,594,347 )     (37,914,629 )
                                 
Provision for income taxes     —         —         —         —    
                                 
Net loss   $ (19,472,645 )   $ (17,832,251 )   $ (67,594,347 )   $ (37,914,629 )
                                 
Loss per share, basic and diluted:                                
                                 
Net loss per share, basic and diluted   $ (0.11 )   $ (0.12 )   $ (0.39 )   $ (0.26 )
                                 
Weighted average number of common                                
  shares outstanding, basic and diluted     177,206,168       152,200,455       171,589,595       147,594,810  

 

 

The accompanying footnotes are an integral part of these consolidated financial statements.

 

4 
 

 

THERAPEUTICSMD, INC. AND SUBSIDIARIES

CONSOLIDATED STATEMENTS OF CASH FLOWS

(Unaudited)

 

  Nine Months Ended
    September 30, 2015   September 30, 2014
         
CASH FLOWS FROM OPERATING ACTIVITIES                
  Net loss   $ (67,594,347 )   $ (37,914,629 )
     Adjustments to reconcile net loss to net cash used in                
        operating activities:                
          Depreciation     22,104       22,713  
          Amortization of intangible assets     22,296       17,196  
          Provision for doubtful accounts     37,163       2,594  
          Share-based compensation     4,740,906       3,934,836  
          Amortization of deferred financing costs     —         260,027  
          Changes in operating assets and liabilities:                
             Accounts receivable     (1,549,532 )     (460,565 )
             Inventory     312,054       31,673  
             Other current assets     (621,923 )     197,569  
             Other assets     (15,162 )     (17,069 )
             Accounts payable     (1,025,504 )     3,534,462  
             Deferred revenue     (522,613 )     (754,431 )
             Other current liabilities     2,546,138       909,890  
             Long term accrued expenses     1,213,874       —    
                 
Net cash used in operating activities     (62,434,546 )     (30,235,734 )
                 
CASH FLOWS FROM INVESTING ACTIVITIES                
  Patent costs     (117,992 )     (193,349 )
  Purchase of property and equipment     (15,559 )     (30,962 )
                 
Net cash used in investing activities     (133,551 )     (224,311 )
                 
CASH FLOWS FROM FINANCING ACTIVITIES                
  Proceeds from sale of common stock, net of costs     91,374,649       42,771,353  
  Proceeds from exercise of options     589,829       315,546  
  Proceeds from exercise of warrants     366,000       181,000  
                 
Net cash provided by financing activities     92,330,478       43,267,899  
                 
Increase in cash     29,762,381       12,807,854  
Cash, beginning of period     51,361,607       54,191,260  
Cash, end of period   $ 81,123,988     $ 66,999,114  

 

 

The accompanying footnotes are an integral part of these consolidated financial statements

 

5 
 

 

 THERAPEUTICSMD, INC. AND SUBSIDIARIES

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Unaudited) 

 

NOTE 1 – THE COMPANY

 

TherapeuticsMD, Inc., a Nevada corporation, or TherapeuticsMD or the Company, has three wholly owned subsidiaries, vitaMedMD, LLC, a Delaware limited liability company, or VitaMed, BocaGreenMD, Inc., a Nevada corporation, or BocaGreen, and VitaCare Prescription Services, Inc., a Florida corporation, or VitaCare. Unless the context otherwise requires, TherapeuticsMD, VitaMed, BocaGreen, and VitaCare collectively are sometimes referred to as "our company," "we," "our," or "us."

 

Nature of Business

 

We are a women’s health care product company focused on creating and commercializing products targeted exclusively for women. As of the date of these unaudited consolidated financial statements, we are focused on conducting the clinical trials necessary for regulatory approval and commercialization of our advanced hormone therapy pharmaceutical products. The drug candidates used in our clinical trials are designed to alleviate the symptoms of and reduce the health risks resulting from menopause-related hormone deficiencies, including hot flashes, osteoporosis, and vaginal discomfort. We are developing these hormone therapy drug candidates, which contain estradiol and progesterone alone or in combination, with the aim of demonstrating equivalent clinical efficacy at lower doses, thereby enabling an enhanced side effect profile compared with competing products. Our drug candidates are created from a platform of hormone technology that enables the administration of hormones with high bioavailability alone or in combination. In addition, we manufacture and distribute branded and generic prescription prenatal vitamins, as well as over-the-counter, or OTC, vitamins.

 

NOTE 2 – BASIS OF PRESENTATION AND RECENTLY ISSUED ACCOUNTING PRONOUNCEMENTS

 

Interim Financial Statements

 

The accompanying unaudited interim consolidated financial statements of TherapeuticsMD, Inc., which include our wholly owned subsidiaries, should be read in conjunction with the audited consolidated financial statements and notes thereto included in our Annual Report on Form 10-K for the year ended December 31, 2014, as filed with the Securities and Exchange Commission, or the SEC, from which we derived the accompanying consolidated balance sheet as of December 31, 2014. The accompanying unaudited interim consolidated financial statements have been prepared in accordance with accounting principles generally accepted in the United States of America, or GAAP, for interim financial information and with the instructions to Form 10-Q and Article 10 of Regulation S-X. Accordingly, since they are interim statements, the accompanying unaudited interim consolidated financial statements do not include all of the information and notes required by GAAP for complete financial statements. The accompanying unaudited interim consolidated financial statements reflect all adjustments, consisting of normal recurring adjustments, that are, in the opinion of our management, necessary to a fair statement of the results for the interim periods presented. Interim results are not necessarily indicative of results for a full year, or any other interim period.

 

6 
 

 

THERAPEUTICSMD, INC. AND SUBSIDIARIES

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Unaudited) 

 

NOTE 2 – BASIS OF PRESENTATION AND RECENTLY ISSUED ACCOUNTING PRONOUNCEMENTS (Continued)

 

Recently Issued Accounting Pronouncements

 

In July 2015, the Financial Accounting Standards Board, or FASB, issued final guidance that requires entities to measure inventory at the lower of cost or net realizable value rather than at the lower of cost or market (LOCOM). The guidance applies only to inventories for which cost is determined by methods other than last-in first-out (LIFO) or the retail inventory method (RIM). Entities that use LIFO or RIM will continue to use existing impairment models. The new guidance does not change the calculation of net realizable value that entities are required to calculate when applying existing LOCOM guidance. Net realizable value is the estimated selling price in the ordinary course of business, less reasonably predictable costs of completion, disposal and transportation. Under the new guidance, however, entities will no longer need to calculate other measures of “market.” The guidance is effective for public business entities for fiscal years beginning after December 15, 2016, and interim periods within those fiscal years. Early adoption is permitted. We are currently evaluating the impact of this guidance on our consolidated financial statements and disclosures.

 

In June 2015, the FASB issued Accounting Standards Update, or ASU, No. 2015-10, Technical Corrections and Improvements, to correct differences between original guidance and the Accounting Standards Codification, or ASC, clarify the guidance, correct references and make minor improvements affecting a variety of topics. Amendments that the FASB deemed more substantive are effective for fiscal years, and interim periods within those fiscal years, beginning after December 15, 2015. The other amendments are effective immediately. We do not expect the adoption of ASU 2015-10 to have a material effect on our consolidated financial statements and disclosures.

 

In August 2014, the FASB issued ASU No. 2014-15, Presentation of Financial Statements-Going Concern (Subtopic 205-40): Disclosure of Uncertainties about an Entity’s Ability to Continue as a Going Concern. ASU 2014-15 requires management to evaluate whether there are conditions and events that raise substantial doubt about the entity’s ability to continue as a going concern within one year after the financial statements are issued (or available to be issued when applicable) and, if so, disclose that fact. ASU 2014-15 is effective for annual periods ending after December 15, 2016 and interim periods within annual periods beginning after December 15, 2016. Early adoption is permitted for annual or interim reporting periods for which the financial statements have not previously been issued. We do not expect the adoption of ASU 2014-15 to have a material effect on our consolidated financial statements and disclosures.

 

In May 2014, the FASB and the International Accounting Standards Board (IASB) issued ASU No. 2014-09, Revenue from Contracts with Customers (Topic 606). The standard’s core principle is that a company will recognize revenue when it transfers promised goods or services to customers in an amount that reflects the consideration to which the company expects to be entitled in exchange for those goods or services. In doing so, companies will need to use more judgment and make more estimates than under previous guidance. These may include identifying performance obligations in the contract, estimating the amount of variable consideration to include in the transaction price and allocating the transaction price to each separate performance obligations. In July 2015, the FASB approved the proposal to defer the effective date of ASU 2014-09 standard by one year. Early adoption is permitted after December 15, 2016, and the standard is effective for public entities for annual reporting periods beginning after December 15, 2017 and interim periods therein. We are currently evaluating the impact of ASU 2014-09 on our consolidated financial statements and disclosures.

 

We do not believe there would have been a material effect on the accompanying consolidated financial statements had any other recently issued, but not yet effective, accounting standards been adopted in the current period.

 

7 
 

 

THERAPEUTICSMD, INC. AND SUBSIDIARIES

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Unaudited) 

 

NOTE 3 – SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES

 

Impairment of Long-Lived Assets

 

We review the carrying values of property and equipment and long-lived intangible assets for impairment whenever events or changes in circumstances indicate that their carrying values may not be recoverable. There was no impairment of any long-lived assets during the three and nine months ended September 30, 2015 and 2014.

 

Fair Value of Financial Instruments

 

Our financial instruments consist primarily of accounts receivable, accounts payable and accrued expenses. The carrying amount of accounts receivable, accounts payable and accrued expenses approximates their fair value because of the short-term maturity of such instruments.

 

We categorize our assets and liabilities that are valued at fair value on a recurring basis into a three-level fair value hierarchy as defined by ASC 820, Fair Value Measurements. The fair value hierarchy gives the highest priority to quoted prices in active markets for identical assets and liabilities (Level 1) and lowest priority to unobservable inputs (Level 3). Assets and liabilities recorded in the consolidated balance sheet at fair value are categorized based on a hierarchy of inputs, as follows:

  

  Level 1 unadjusted quoted prices in active markets for identical assets or liabilities;
  Level 2 quoted prices for similar assets or liabilities in active markets or inputs that are observable for the asset or liability, either directly or indirectly through market corroboration, for substantially the full term of the financial instrument; and
  Level 3 unobservable inputs for the asset or liability.

 

At September 30, 2015 and December 31, 2014, we had no assets or liabilities that were valued at fair value on a recurring basis.

 

The fair value of indefinite-lived assets or long-lived assets is measured on a non-recurring basis using significant unobservable inputs (Level 3) in connection with any required impairment test.

 

Revenue Recognition

 

We recognize revenue on arrangements in accordance with ASC 605, Revenue Recognition. We recognize revenue only when the price is fixed or determinable, persuasive evidence of an arrangement exists, the service is performed, and collectability is reasonably assured.

 

Our OTC and prescription prenatal vitamin products are generally variations of the same product with slight modifications in formulation and marketing. The primary difference between our OTC and prescription prenatal vitamin products is the source of payment. Purchasers of our OTC prenatal vitamin products pay for the product directly while purchasers of our prescription prenatal vitamin products pay for the product via third-party payers. Both OTC and prescription prenatal vitamin products share the same marketing support team utilizing similar marketing techniques.

 

Over-the-Counter Products

 

We generate OTC revenue from product sales primarily to retail consumers. We recognize revenue from product sales upon shipment, when the rights of ownership and risk of loss have passed to the consumer. We include outbound shipping and handling fees in revenues, net, and bill them upon shipment. We include shipping expenses in cost of goods sold. A majority of our customers pay for our products with credit cards, and we usually receive the cash settlement in two to three banking days. Credit card sales minimize accounts receivable balances relative to sales. We provide an unconditional 30-day money-back return policy under which we accept product returns from our retail and eCommerce customers. We recognize our revenue from OTC sales, net of estimated returns, sales discounts, and eCommerce fees.

 

8 
 

 

THERAPEUTICSMD, INC. AND SUBSIDIARIES

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Unaudited) 

 

 

Prescription Products

 

We sell our name brand and generic prescription products primarily through drug wholesalers and retail pharmacies. We recognize revenue from prescription product sales, net of sales discounts, chargebacks, and customer rebates.

 

We accept returns of unsalable product from customers within a return period of six months prior to and up to 12 months following product expiration. Our prescription products currently have a shelf life of 24 months from the date of manufacture. As of January 1, 2015, we started estimating returns based on historical return rates and recorded actual product returns against this reserve as received. Prior to January 1, 2015, we deferred the recognition of revenue on certain arrangements until the right of return no longer existed.

 

We maintain various rebate programs in an effort to maintain a competitive position in the marketplace and to promote sales and customer loyalty. The consumer rebate program is designed to enable the end user to submit a coupon to us. If the coupon qualifies, we send a rebate check to the end user. We estimate the allowance for consumer rebates based on our experience and industry averages, which is reviewed, and adjusted if necessary, on a quarterly basis.

 

Research and Development Expenses

 

Research and development, or R&D, expenses include internal R&D activities, services of external contract research organizations, or CROs, costs of their clinical research sites, manufacturing, scale-up and validation costs, and other activities. Internal R&D activity expenses include laboratory supplies, salaries, benefits, and non-cash share-based compensation expenses. Advance payments to be expensed in future research and development activities were $948,499 at September 30, 2015, of which $755,152 was included in Other current assets and $193,347 was included in long term Prepaid expense on the accompanying consolidated balance sheets. Advance payments to be expensed in future research and development activities were $1,175,082 at December 31, 2014, of which $711,362 was included in Other current assets and $463,720 was included in long term Prepaid expense on the accompanying consolidated balance sheets. CRO activity expenses include preclinical laboratory experiments and clinical trial studies. Other activity expenses include regulatory consulting and legal fees and costs. The activities undertaken by our regulatory consultants that were classified as research and development expenses include assisting, consulting with, and advising our in-house staff with respect to various FDA submission processes, clinical trial processes, and scientific writing matters, including preparing protocols and FDA submissions. Legal activities that were classified as research and development expenses related to designing experiments to generate data for patents and to further the formulation development process for our pipeline technologies. Outside legal counsel also provided professional research and advice regarding research and development, patents and regulatory matters. These consulting and legal expenses were direct costs associated with preparing, reviewing, and undertaking work for our clinical trials and investigative drugs. We charge internal R&D activities and other activity expenses to operations as incurred. We make payments to CROs based on agreed-upon terms, which may include payments in advance of a study starting date. We expense nonrefundable advance payments for goods and services that will be used in future R&D activities when the activity has been performed or when the goods have been received rather than when the payment is made. We review and accrue CRO expenses and clinical trial study expenses based on services performed and rely on estimates of those costs applicable to the completion stage of a study as provided by CROs. As of September 30, 2015, we classified $1,213,874 of the accrued clinical study costs as long term Accrued Expenses related to the costs that will be paid at the completion of one of our clinical trials. Estimated accrued CRO costs are subject to revisions as such studies progress to completion. We charge revisions expense in the period in which the facts that give rise to the revision become known.

 

9 
 

 

THERAPEUTICSMD, INC. AND SUBSIDIARIES

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Unaudited) 

 

Segment Reporting

 

We are managed and operated as one business, which is focused on creating and commercializing products targeted exclusively for women. Our business operations are managed by a single management team that reports to the President of our Company. We do not operate separate lines of business with respect to any of our products and we do not prepare discrete financial information with respect to separate products. All product sales are derived from sales in the United States. Accordingly, we view our business as one reportable operating segment.

 

NOTE 4 – INVENTORY

 

Inventory consists of the following:

 

   

September 30,

2015

 

December 31,

2014

Finished product   $ 787,232     $ 874,294  
Raw material     82,827       155,341  
Deferred costs     —         152,478  
     TOTAL INVENTORY   $ 870,059     $ 1,182,113  

 

NOTE 5 – OTHER CURRENT ASSETS

 

Other current assets consist of the following:

   

September 30,

2015

 

December 31,

2014

Prepaid insurance   $ 870,949     $ 394,878  
Prepaid research and development costs     381,813       299,498  
Prepaid consulting     373,339       411,864  
Other receivables-related party (Note 13)     249,981       249,981  
Other prepaid costs     219,086       181,186  
Prepaid vendor deposits     25,637       —    
     TOTAL OTHER CURRENT ASSETS   $ 2,120,805     $ 1,537,407  

 

NOTE 6 – FIXED ASSETS, NET

 

Fixed assets, net consist of the following:

   

September 30,

2015

 

December 31,

2014

Equipment   $ 132,150     $ 132,150  
Furniture and fixtures     69,454       53,895  
      201,604       186,045  
Accumulated depreciation     (144,856 )     (122,752 )
     TOTAL FIXED ASSETS, NET   $ 56,748     $ 63,293  

 

Depreciation expense for the three months ended September 30, 2015 and 2014 was $7,856 and $7,122, respectively, and $22,104 and $22,713 for the nine months ended September 30, 2015 and 2014, respectively.

 

10 
 

 

THERAPEUTICSMD, INC. AND SUBSIDIARIES

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Unaudited) 

 

NOTE 7 – PREPAID EXPENSE

 

Prepaid expense (long-term) consists of the following:

   

September 30,

2015

 

December 31,

2014

Prepaid manufacturing costs   $ 978,704     $ 963,543  
Prepaid research and development costs     193,347       463,720  
     TOTAL PREPAID EXPENSE   $ 1,172,051     $ 1,427,263  

 

NOTE 8 – INTANGIBLE ASSETS, NET

 

The following table sets forth the gross carrying amount, accumulated amortization and net carrying amount of our intangible assets as of September 30, 2015 and December 31, 2014:

 

    September 30, 2015
   

 

Gross Carrying Amount

 

 

Accumulated Amortization

 

 Net

Amount

  Weighted- Average Amortization Period (yrs.)
Amortizing intangible assets:                                
   OPERA® software patent   $ 31,951     $ (3,994 )   $ 27,957       14  
   Development costs of                                
      corporate website     91,743       (91,743 )     —         n/a  
   Approved hormone                                
      therapy drug                                
      candidate patents     605,502       (40,199 )     565,303       17.25  
Non-amortizing intangible                                
  assets:                                
   Hormone therapy drug                                
      candidate patents                                
      (pending)     585,241       —         585,241       n/a  
   Multiple trademarks for                                
      vitamins/supplements     145,783       —         145,783       indefinite  
      Total   $ 1,460,220     $ (135,936 )   $ 1,324,284          

 

 

11 
 

 

THERAPEUTICSMD, INC. AND SUBSIDIARIES

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Unaudited) 

 

   

 December 31, 2014

   

 

Gross Carrying Amount

 

 

Accumulated Amortization

 

 Net

Amount

  Weighted- Average Amortization Period (yrs.)
Amortizing intangible assets:                                
   OPERA® software patent   $ 31,951     $ (2,496 )   $ 29,455       14.75  
   Development costs of                                
      corporate website     91,743       (91,743 )     —         n/a  
   Approved hormone                                
      therapy drug                                
      candidate patents     439,184       (19,401 )     419,783       18  
Non-amortizing intangible                                
  assets:                                
   Hormone therapy drug                                
      candidate patents                                
      (pending)     675,982       —         675,982       n/a  
   Multiple trademarks for                                
      vitamins/supplements     103,368       —         103,368       indefinite  
      Total   $ 1,342,228     $ (113,640 )   $ 1,228,588          

 

We capitalize external costs, consisting primarily of legal costs, related to securing our patents and trademarks. Once a patent is granted, we amortize the capitalized patent costs over the remaining life of the patent using the straight-line method. If the patent is not granted, we write-off any capitalized patent costs at that time.

 

Trademarks are perpetual and are not amortized. As of September 30, 2015, the remaining life related to OPERA® patent was approximately 14 years and the remaining life related to the approved hormone therapy drug candidate patents was approximately 17 years. During the three and nine months ended September 30, 2015 and 2014, there was no impairment recognized.

 

In addition to numerous pending patent applications, as of September 30, 2015, we had 13 issued patents, including:

one method patent that relates to our OPERA® information technology platform, which is owned by us and is a U.S. jurisdiction patent with an expiration date in 2029;
  twelve utility patents that relate to our combination progesterone and estradiol formulations, which are owned by us and are U.S. jurisdiction patents with expiration dates in 2032. We have pending patent applications with respect to certain of these patents in Argentina, Australia, Canada, the European Union, Israel, Mexico, Brazil, Japan, Russia, South Africa and South Korea.

 

Amortization expense was $8,692 and $5,625 for the three months ended September 30, 2015 and 2014, respectively and $22,296 and $17,196 for the nine months ended September 30, 2015 and 2014, respectively. Estimated amortization expense for the next five years is as follows:

 

Year Ending December 31,   Estimated Amortization
  2015 (3 months)     $ 8,692  
  2016     $ 34,768  
  2017     $ 34,768  
  2018     $ 34,768  
  2019     $ 34,768  

 

12 
 

 

 THERAPEUTICSMD, INC. AND SUBSIDIARIES

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Unaudited) 

 

NOTE 9 – OTHER CURRENT LIABILITIES

 

Other current liabilities consist of the following:

   

September 30,

2015

 

December 31,

2014

Accrued clinical trial costs   $ 3,528,061     $ 1,706,542  
Accrued payroll, bonuses and commission costs     930,913       814,205  
Accrued legal and accounting expense     615,946       276,470  
Accrued compensated absences     490,170       442,430  
Other accrued expenses     388,268       185,965  
Allowance for coupons and returns     208,361       90,446  
Allowance for wholesale distributor fees     96,440       160,503  
Accrued rent     86,998       91,368  
Accrued royalties     41,620       72,710  
     TOTAL OTHER CURRENT LIABILITIES   $ 6,386,777     $ 3,840,639  

 

NOTE 10 – NET LOSS PER SHARE

 

We calculate basic and diluted net loss per share allocable to common stockholders using the weighted-average number of shares of common stock, par value $0.001 per share, or Common Stock outstanding during the period, less any shares subject to repurchase or forfeiture. There were no shares of our Common Stock outstanding subject to repurchase or forfeiture for the three and nine months ended September 30, 2015 and 2014.

 

Since we are in a net loss position, we have excluded outstanding stock options, all of which are subject to forfeiture, as well as warrants for the purchase of our Common Stock from our calculation of diluted net loss per share.

 

The table below presents the potentially dilutive securities that would have been included in our calculation of diluted net loss per share allocable to common stockholders if they were not antidilutive for the periods presented.

 

    As of September 30,
    2015   2014
Stock options     17,414,242       16,851,943  
Warrants     12,722,431       13,927,916  
      30,136,673       30,779,859  

 

NOTE 11 – STOCKHOLDERS’ EQUITY

 

Preferred Stock

 

At September 30, 2015, we had 10,000,000 shares of Preferred Stock, par value $0.001, authorized for issuance, of which no shares of Preferred Stock were issued or outstanding.

 

 

13 
 

THERAPEUTICSMD, INC. AND SUBSIDIARIES

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Unaudited) 

 

Common Stock

 

At September 30, 2015, we had 350,000,000 shares of Common Stock authorized, of which 177,787,927 shares of Common Stock were issued and outstanding.

 

On July 9, 2015, we entered into an underwriting agreement with Stifel, Nicolaus & Company, Incorporated and Guggenheim Securities, LLC, as the representatives of the several underwriters, or the Stifel Underwriters, relating to an underwritten public offering of 3,846,154 shares of Common Stock at a public offering price of $7.80 per share. Under the terms of the underwriting agreement, we granted the Stifel Underwriters a 30-day option to purchase up to an aggregate of 576,923 additional shares of Common Stock, which option was exercised in full. The net proceeds to us from the offering were approximately $32.2 million, after deducting underwriting discounts and commissions and other estimated offering expenses payable by us. The offering closed on July 15, 2015 and we issued 4,423,077 shares of our Common Stock.

 

On February 10, 2015, we entered into an underwriting agreement, or the Cowen Agreement, with Cowen and Company, LLC, as the representative of the several underwriters, or the Cowen Underwriters, relating to an underwritten public offering of 13,580,246 shares of Common Stock, at a public offering price of $4.05 per share. Under the terms of the Cowen Agreement, we granted the Cowen Underwriters a 30-day option to purchase up to an aggregate of 2,037,036 additional shares of Common Stock, which option was exercised in full. The net proceeds from the offering were approximately $59.1 million, after deducting underwriting discounts and commissions and other estimated offering expenses payable by us. The offering closed on February 17, 2015 and we issued 15,617,282 shares of our Common Stock.

 

On July 29, 2014, we entered into an underwriting agreement with Goldman Sachs & Co, or Goldman Sachs, as the representative of the underwriters named therein, or the Goldman Sachs Underwriters, relating to an underwritten public offering of 8,565,310 shares of Common Stock. The price to the public in the offering was $4.67 per share. Under the terms of the underwriting agreement, we granted the Goldman Sachs Underwriters a 30-day option to purchase up to an additional 1,284,796 shares of Common Stock. On July 30, 2014, the Goldman Sachs Underwriters exercised their option to purchase the additional 1,284,796 shares of Common Stock. Net proceeds from this offering were approximately $42.8 million, after deducting underwriting discounts and commissions and other offering expenses. The offering closed on August 4, 2014 and we issued 9,850,106 shares of our Common Stock.

 

Exercises During 2015

 

During the three months ended September 30, 2015, certain individuals exercised stock options to purchase 95,000 shares of Common Stock for $98,478 in cash. During the nine months ended September 30, 2015, certain individuals exercised stock options to purchase 472,867 shares of Common Stock for $589,829 in cash.

 

Exercises During 2014

 

During the nine months ended September 30, 2014, certain individuals exercised stock options to purchase 793,800 shares of Common Stock. Stock options to purchase shares of Common Stock were exercised as follows: (i) 674,193 options for $315,546 in cash and (ii) 119,607 options, pursuant to the stock options’ cashless provision, wherein 113,837 shares of Common Stock were issued. Also during the nine months ended September 30, 2014, we issued 50,000 shares of Common Stock to an employee upon the vesting of restricted stock units that were granted in December 2013.

 

Warrants to Purchase Common Stock

 

As of September 30, 2015, we had warrants outstanding to purchase an aggregate of 12,772,431 shares of Common Stock with a weighted-average contractual remaining life of 1.92 years, and exercise prices ranging from $0.24 to $6.35 per share, resulting in a weighted average exercise price of $1.93 per share.

 

14 
 

 

THERAPEUTICSMD, INC. AND SUBSIDIARIES

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Unaudited) 

 

The valuation methodology used to determine the fair value of our warrants is the Black-Scholes-Merton valuation model, or the Black-Scholes Model. The Black-Scholes Model requires the use of a number of assumptions, including volatility of the stock price, the risk-free interest rate and the term of the warrant.

 

In January 2013, we granted warrants to purchase 1,250,000 shares of Common Stock in connection with the issuance of a Revolving Credit Note to Plato and Associates, LLC, or the Plato Warrant. The Plato Warrant has an exercise price of $3.20 per share. The Plato Warrant vested on October 31, 2013 and may be exercised prior to its expiration on January 31, 2019. The Plato Warrant, with a fair value of $1,711,956, was valued on the date of the grant using a term of six years; a volatility of 44.29%; risk free rate of 0.88%; and a dividend yield of 0%. For the nine months ended September 30, 2015 and 2014, $0 and $260,027, respectively, was recorded as financing costs in connection with the issuance of the Plato Warrant on the accompanying consolidated financial statements.

 

In May 2013, we entered into a consulting agreement with Sancilio & Company, Inc., or SCI, to develop drug technology to be used in our hormone replacement drug candidates. These services include support of our efforts to successfully obtain U.S. Food and Drug Administration, or the FDA, approval for our drug candidates, including a vaginal capsule for the treatment of vulvar and vaginal atrophy, or VVA. In connection with the agreement, SCI agreed to forfeit its rights to receive warrants to purchase 833,000 shares of Common Stock that were to be granted pursuant to the terms of a prior consulting agreement dated May 17, 2012. As consideration under the agreement, we agreed to grant to SCI a warrant to purchase 850,000 shares of Common Stock at $2.01 per share that has vested or will vest, as applicable, as follows:

 

  1. 283,333 shares were earned on May 11, 2013 upon acceptance of an Investigational New Drug application by the FDA for an estradiol-based drug candidate in a softgel vaginal capsule for the treatment of VVA; however, pursuant to the terms of the consulting agreement, the shares did not vest until June 30, 2013.  The fair value of $405,066 for the shares vested on June 30, 2013 was determined by using the Black-Scholes Model on the date of vesting using a term of five years; a volatility of 45.89%; risk free rate of 1.12%; and a dividend yield of 0%.  We recorded the entire $405,066 as non-cash compensation as of June 30, 2013;

 

  2. 283,333 shares vested on June 30, 2013.  The fair value of $462,196 for these shares was determined by using the Black-Scholes Model on the date of the vesting using a term of five years; a volatility of 45.84%; risk free rate of 1.41%; and a dividend yield of 0%.  As of September 30, 2015, we recorded $115,543 in other current assets in the accompanying consolidated financial statements with respect to such shares.  During the three and nine month periods ended September 30, 2015 and 2014, we recorded $38,517 and $115,551, respectively, as non-cash compensation in the accompanying consolidated financial statements with respect to such shares; and

 

  3. 283,334 shares will vest upon the receipt by us of any final FDA approval of a drug candidate that SCI helped us design.  It is anticipated that this event will not occur before December 2016.

 

As of September 30, 2015, unamortized costs associated with the SCI warrants issued in 2013 and 2012 totaled approximately $567,000 and will be recognized over a period of 1.75 years.

 

During the nine months ended September 30, 2015, we granted warrants to purchase 50,000 shares of Common Stock to an outside consultant at an exercise price of $6.35 and the expiration date of April 6, 2020. The total non-cash compensation expense related to this warrant was $42,266 and $86,008, respectively, for the three and nine months ended September 30, 2015.

 

15 
 

 

THERAPEUTICSMD, INC. AND SUBSIDIARIES

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Unaudited) 

 

Warrant exercises

 

During the three months ended September 30, 2015, certain individuals and an entity exercised warrants to purchase 310,000 shares of Common Stock pursuant to the warrants’ cashless exercise provisions, wherein 232,197 shares of Common Stock were issued. During the nine months ended September 30, 2015, certain individuals and an entity exercised warrants to purchase 1,255,485 shares of Common Stock as follows: (i) 945,485 shares of Common Stock were issued for $366,000 in cash and (ii) warrants to purchase 310,000 shares of Common Stock were exercised pursuant to the warrants’ cashless exercise provisions, wherein 232,197 shares of Common Stock were issued.

 

During the nine months ended September 30, 2014, certain individuals exercised warrants to purchase 365,583 shares of Common Stock for $181,000 in cash.

 

Options to Purchase Common Stock

 

In 2009, we adopted the 2009 Long Term Incentive Compensation Plan, or the 2009 Plan, to provide financial incentives to employees, directors, advisers, and consultants of our company who are able to contribute towards the creation of or who have created stockholder value by providing them stock options and other stock and cash incentives, or the Awards. The Awards available under the 2009 Plan consist of stock options, stock appreciation rights, restricted stock, restricted stock units, performance stock, performance units, and other stock or cash awards as described in the 2009 Plan. There are 25,000,000 shares authorized for issuance thereunder. During the nine months ended September 30, 2015, we granted 1,231,000 non-qualified stock options under the 2009 Plan. As of September 30, 2015, there were non-qualified stock options to purchase 15,445,768 shares of Common Stock outstanding under the 2009 Plan.

 

In 2012, we adopted the 2012 Stock Incentive Plan, or the 2012 Plan, a non-qualified plan that was amended in August 2013. The 2012 Plan was designed to serve as an incentive for retaining qualified and competent key employees, officers, directors, and certain consultants and advisors of our company. There are 10,000,000 shares of Common Stock authorized for issuance thereunder. As of September 30, 2015, there were non-qualified stock options to purchase 1,968,474 shares of Common Stock outstanding under the 2012 Plan.

 

The valuation methodology used to determine the fair value of stock options is the Black-Scholes Model. The Black-Scholes Model requires the use of a number of assumptions including estimated volatility of the stock price, the risk-free interest rate, and the expected life of the stock options. The assumptions used in the Black-Scholes Model during the nine months ended September 30, 2015 and 2014 are set forth in the table below.

 

    Nine Months Ended September 30,
    2015   2014
Risk-free interest rate     1.47-1.54 %     1.68-1.77 %
Volatility     58.77-62.94 %     69.15-70.93 %
Term (in years)     5.27-6.25       5-6.25  
Dividend yield     0.00 %     0.00 %

 

The risk-free interest rate assumption is based upon observed interest rates on zero coupon U.S. Treasury bonds whose maturity period is appropriate for the expected term. Estimated volatility is a measure of the amount by which the price of our Common Stock is expected to fluctuate each year during the term of an award. Our estimated volatility is an average of the historical volatility of the stock prices of our peer entities whose stock prices were publicly available. Our calculation of estimated volatility is based on historical stock prices over a period equal to the term of the awards. We used the historical volatility of our peer entities due to the lack of sufficient historical data on our stock price. The average expected life is based on the contractual terms of the stock option using the simplified method.

 

16 
 

 

 

THERAPEUTICSMD, INC. AND SUBSIDIARIES

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Unaudited) 

 

 

A summary of activity under the 2009 and 2012 Plans and related information follows:

 

    Number of Shares Underlying Stock Options  

 

Weighted Average Exercise Price

 

Weighted Average

Remaining

Contractual

Life in Years

 

 

 

Aggregate Intrinsic Value

Balance at December 31, 2014     16,792,443     $ 1.88       6.92     $ 43,996,311  
   Granted     1,231,000     $ 6.38                  
   Exercised     (472,867 )   $ 1.25                  
   Expired/Forfeited     (136,334 )   $ 3.01                  
Balance at September 30, 2015     17,414,242     $ 2.21       6.09     $ 64,265,785  

Vested and Exercisable at September 30, 2015

    13,848,923     $ 1.59       5.49     $ 59,095,453  

 

At September 30, 2015, our outstanding stock options had exercise prices ranging from $0.10 to $7.72 per share.

 

Share-based compensation expense for options recognized in our results of operations (based on vested awards) for the three and nine months ended September 30, 2015 were $1,626,862 and $4,328,964, respectively, and $1,047,493 and $3,341,604, respectively, for the same periods in 2014. ASC 718-10 requires forfeitures to be estimated at the time of grant and revised in subsequent periods if actual forfeitures differ from the estimates. At September 30, 2015, total unrecognized estimated compensation expense related to unvested options granted prior to that date was approximately $5,593,000 which may be adjusted for future changes in forfeitures. This cost is expected to be recognized over a weighted-average period of 2.3 years. No tax benefit was realized due to a continued pattern of operating losses.

 

NOTE 12 – INCOME TAXES

 

Deferred income tax assets and liabilities are determined based upon differences between the financial reporting and tax basis of assets and liabilities and are measured using the enacted tax rates and laws that will be in effect when the differences are expected to reverse. We do not expect to pay any significant federal or state income tax for 2015 as a result of (i) the losses recorded during the nine months ended September 30, 2015, (ii) additional losses expected for the remainder of 2015, and/or (iii) net operating loss carry forwards from prior years. Accounting standards require the consideration of a valuation allowance for deferred tax assets if it is "more likely than not" that some component or all of the benefits of deferred tax assets will not be realized. As of September 30, 2015, we maintain a full valuation allowance for all deferred tax assets. Based on these requirements, no provision or benefit for income taxes has been recorded. There were no recorded unrecognized tax benefits at the end of the reporting period.

 

NOTE 13 – RELATED PARTIES

 

On February 29, 2012, Cooper C. Collins, who was then president and largest shareholder of Pernix Therapeutics, LLC, or Pernix, was elected to serve on our board of directors. From time to time, we have entered into agreements with Pernix in the normal course of business. All such agreements are reviewed by independent directors of our company or a committee consisting of independent directors of our company.

 

17 
 

 

THERAPEUTICSMD, INC. AND SUBSIDIARIES

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Unaudited) 

 

During the nine months ended September 30, 2015 and 2014, we did not engage in any transactions with Pernix. At September 30, 2015 and December 31, 2014, there were amounts due Pernix of approximately $46,000.

 

Additionally, there were amounts due to us from Pernix for legal fee reimbursement relating to a litigation matter stemming from a license and supply agreement in the amounts of approximately $250,000 at both September 30, 2015 and December 31, 2014.

 

NOTE 14 - BUSINESS CONCENTRATIONS

 

We purchase our products from several suppliers with approximately 54% and 77% of our purchases supplied from one vendor for the nine months ended September 30, 2015 and 2014, respectively.

 

We sell our prescription prenatal vitamin products to wholesale distributors, specialty pharmacies, specialty distributors, and chain drug stores that generally sell products to retail pharmacies, hospitals, and other institutional customers. Revenue generated from four major customers accounted for approximately 90% and 95% of our recognized revenue for the nine months ended September 30, 2015 and 2014, respectively.

 

Customers that generated more than 10% of our sales are designated as customers “A”, “B”, “C” and “D”.  During the nine months ended September 30, 2015, two customers generated more than 10% of revenues and during the nine months ended September 30, 2014, four customers generated more than 10% of revenues. During the nine months ended September 30, 2015, customer A generated approximately $6,930,000 in revenues and customer B generated approximately $3,005,000 in revenues. During the nine months ended September 30, 2014, customers A, B, C and D generated approximately $3,930,000, $1,846,000, $1,590,000 and $1,555,000 in sales, respectively.

 

NOTE 15 – COMMITMENTS AND CONTINGENCIES

 

We lease administrative office space in Boca Raton, Florida pursuant to a 63 month non-cancelable operating lease that commenced on July 1, 2013 and expires on September 30, 2018. On February 18, 2015, we entered into an agreement to lease additional administrative office space in Boca Raton, Florida, pursuant to an addendum to such lease. This addendum was effective beginning April 1, 2015 and will expire with the original lease term on September 30, 2018.

 

The straight line rental expense related to our current lease totaled approximately $119,000 and $90,000 for the three months ended September 30, 2015 and 2014, respectively, and approximately $328,000 and $271,000 for the nine months ended September 30, 2015 and 2014, respectively. The 2014 amounts were partially offset by the rent income of approximately $6,000 and $42,000, respectively, for sublet space. We did not sublet any space during the nine months ended September 30, 2015.

 

As of September 30, 2015, future minimum rental payments are as follows:

 

Years Ending December 31,    
  2015 (3 months)     $ 121,698  
  2016       493,790  
  2017       507,087  
  2018       388,976  
  Minimum lease payments     $ 1,511,551  

 

NOTE 16 – SUBSEQUENT EVENTS

 

In October 2015, we completed enrollment in the REPLENISH trial, a phase 3 study of TX-001HR in postmenopausal women with an intact uterus. The trial was designed to enroll approximately 1,750 patients at approximately 100 sites.

 

18 
 

 

Item 2. Management's Discussion and Analysis of Financial Condition and Results of Operations

 

General

 

The following discussion and analysis provides information that we believe to be relevant to an assessment and understanding of our results of operations and financial condition for the periods described. This discussion should be read together with our consolidated financial statements and the notes to the consolidated financial statements, which are included in this Quarterly Report on Form 10-Q. This information should also be read in conjunction with the information contained in our Annual Report on Form 10-K for the year ended December 31, 2014 filed with the Securities and Exchange Commission, or the Commission or the SEC, on March 12, 2015, or the Annual Report, including the audited financial statements and notes included therein. The reported results will not necessarily reflect future results of operations or financial condition.

 

In addition, this Quarterly Report on Form 10-Q contains forward-looking statements that involve substantial risks and uncertainties. Forward-looking statements may include, but are not limited to, statements relating to our objectives, plans and strategies as well as statements, other than historical facts, that address activities, events or developments that we intend, expect, project, believe or anticipate will or may occur in the future. These statements are often characterized by terminology such as “believes,” “hopes,” “may,” “anticipates,” “should,” “intends,” “plans,” “will,” “expects,” “estimates,” “projects,” “positioned,” “strategy” and similar expressions and are based on assumptions and assessments made in light of management’s experience and perception of historical trends, current conditions, expected future developments and other factors believed to be appropriate. Forward-looking statements are made as of the date of this Quarterly Report on Form 10-Q and we undertake no duty to update or revise any such statements, whether as a result of new information, future events or otherwise. Forward-looking statements are not guarantees of future performance and are subject to risks and uncertainties, many of which are outside of our control. Important factors that could cause actual results, developments and business decisions to differ materially from forward-looking statements are described in the sections titled “Risk Factors” in our Annual Report, and include the following: our ability to maintain or increase sales of our products; our ability to develop and commercialize our hormone therapy drug candidates and obtain additional financing necessary therefor; the length, cost and uncertain results of our clinical trials; the potential of adverse side effects or other safety risks that could preclude the approval of our hormone therapy drug candidates; our reliance on third parties to conduct our clinical trials, research and development and manufacturing; the availability of reimbursement from government authorities and health insurance companies for our products; the impact of product liability lawsuits; and the influence of extensive and costly government regulation.

 

Throughout this Quarterly Report on Form 10-Q, the terms "we," "us," "our," "TherapeuticsMD," or "our company" refer to TherapeuticsMD, Inc., a Nevada corporation, and unless specified otherwise, include our wholly owned subsidiaries, vitaMedMD, LLC, a Delaware limited liability company, or VitaMed, BocaGreenMD, Inc., a Nevada corporation, or BocaGreen, and VitaCare Prescription Services, Inc., a Florida corporation, or VitaCare.

 

On June 30, 2015, we exceeded the $750 million public float threshold to trigger “large accelerated filer” reporting status with the SEC beginning in fiscal year 2016. Consequently, as of January 1, 2016, we will no longer be an “accelerated filed” as such term is defined in Rule 12b-2 of the Securities Exchange Act of 1934, as amended, and we will need to comply with the large accelerated filer reporting deadlines for our Annual Report on Form 10-K for the fiscal year ending December 31, 2015, and our Quaterly Reports on Form 10-Q beginning with the quarter ending March 31, 2016.

 

Overview

 

We are a women’s health care company focused on creating and commercializing products targeted exclusively for women. Currently, we are focused on conducting the clinical trials necessary for regulatory approval and commercialization of advanced hormone therapy pharmaceutical products. The current drug candidates used in our clinical trials are designed to alleviate the symptoms of and reduce the health risks resulting from menopause-related hormone deficiencies, including hot flashes, osteoporosis, and vaginal discomfort. We are developing these hormone therapy drug candidates, which contain estradiol and progesterone alone or in combination, with the aim of demonstrating equivalent clinical efficacy at lower doses, thereby enabling an enhanced side effect profile compared with competing products. Our drug candidates are created from hormone technology that enables the administration of hormones with high bioavailability alone or in combination. In addition, we manufacture and distribute branded and generic prescription prenatal vitamins, as well as over-the-counter, or OTC, vitamins.

 

19 
 

 

Our common stock, par value $0.001 per share, or Common Stock, is traded on the NYSE MKT under the symbol “TXMD”. We maintain the following websites at www.therapeuticsmd.com, www.vitamedmd.com, www.vitamedmdrx.com, and www.bocagreenmd.com. The information contained on our websites or that can be accessed through our websites does not constitute part of this Quarterly Report on Form 10-Q.

 

Research and Development

 

Overview

 

We have obtained the U.S. Food and Drug Administration, or FDA, acceptance of our Investigational New Drug, or IND, applications to conduct clinical trials for four of our hormone therapy drug candidates: TX-001HR, our oral combination of progesterone and estradiol; TX-002HR, our oral progesterone alone; TX-003HR, our oral estradiol alone; and TX-004HR, our vaginal estradiol softgel with estradiol alone.

 

We are currently conducting phase 3 clinical trials for TX-001HR and TX-004HR. In July 2014, we temporarily suspended enrollment in the phase 3 clinical trial for TX-002HR, and in October 2014 we temporarily stopped the trial in order to update the phase 3 protocol based on discussions with the FDA. We have no current plans to conduct clinical trials for TX-003HR.

 

TX-001HR, our combination estradiol and progesterone drug candidate, is undergoing clinical trials for the treatment of moderate to severe vasomotor symptoms due to menopause, including hot flashes, night sweats, sleep disturbances, and vaginal discomfort for post-menopausal women with an intact uterus. The hormone therapy drug candidate is chemically identical to the hormones that naturally occur in a woman’s body, namely estradiol and progesterone, and is being studied as a continuous-combined regimen, in which the combination of estrogen and progesterone are taken together in one product daily. If approved by the FDA, we believe this would represent the first time a combination product of estradiol and progesterone (bioidentical to the estradiol and progesterone produced by the ovaries), would be approved for use in a single combined product.

 

On September 5, 2013, we began enrollment of the REPLENISH Trial, a multicenter, double-blind, placebo-controlled, phase 3 study of TX-001HR in postmenopausal women with an intact uterus. The study is designed to evaluate the efficacy of TX-001HR for the treatment of moderate to severe vasomotor symptoms due to menopause and the endometrial safety of TX-001HR. Patients are assigned to one of five treatment arms, four active and one placebo, and receive study medication for 12 months. The primary endpoint for the reduction of endometrial hyperplasia is an incidence of endometrial hyperplasia of less than 1% at 12 months, as determined by endometrial biopsy. The primary endpoint for the treatment of moderate to severe vasomotor symptoms is the mean change of frequency and severity of moderate to severe vasomotor symptoms at weeks four and 12 compared to placebo, as measured by the number and severity of hot flushes. Only subjects experiencing a minimum daily frequency of seven moderate to severe hot flushes at screening are included in the vasomotor symptoms analysis, while all subjects are included in the endometrial hyperplasia analysis. The secondary endpoints include reduction in sleep disturbances and improvement in quality of life measures, night sweats and vaginal dryness, measured at 12 weeks, six months and 12 months. The trial is designed to enroll approximately 1,750 patients at approximately 100 sites. We completed enrollment in the REPLENISH Trial in October 2015 and we currently anticipate that results of the trial will be reported in the fourth quarter of 2016 or the first quarter of 2017. Based on such timeline and successful reports of the trial, we would anticipate filing an NDA for TX-001HR during the fourth quarter of 2016 or the first quarter of 2017 and assuming an FDA review period of ten months from the receipt date to the Prescription Drug User Fee Act, or PDUFA, date for a non-new molecular entity, the NDA for TX-001HR could be approved by the FDA during the fourth quarter of 2017 or the first quarter of 2018.

 

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TX-002HR is a natural progesterone formulation for the treatment of secondary amenorrhea without the potentially allergenic component of peanut oil. The hormone therapy drug candidate is chemically identical to the hormones that naturally occur in a woman’s body. We believe it will be similarly effective to traditional treatments, but may demonstrate efficacy at lower dosages. In January 2014, we began recruitment of patients in the SPRY Trial, a phase 3 clinical trial designed to measure the safety and effectiveness of TX-002HR in the treatment of secondary amenorrhea. During the first two quarters of 2014, the SPRY Trial encountered enrollment challenges because of Institutional Review Board approved clinical trial protocols and FDA inclusion and exclusion criteria. In July 2014, we temporarily suspended enrollment and in October 2014 we temporarily stopped the SPRY Trial in order to update the phase 3 protocol based on discussions with the FDA. We intend to update the phase 3 protocol to, among other things, target only those women with secondary amenorrhea due to polycystic ovarian syndrome and to amend the primary endpoint of the trial. We believe that the updated phase 3 protocol, if approved by the FDA, will allow us to mitigate the enrollment challenges in, and shorten the duration of, the SPRY Trial. However, there can be no assurance that the FDA will approve the updated phase 3 protocol that we intend to propose.

 

TX-004HR is a vaginal estradiol softgel drug candidate for the treatment of vulvar and vaginal atrophy, or VVA, in post-menopausal women with vaginal linings that do not receive enough estrogen. We believe that our drug candidate will be at least as effective as the traditional treatments for VVA because of an early onset of action with less systemic exposure inferring a greater probability of dose administration to the target tissue, and it will have an added advantage of being a simple, easier to use dosage form versus traditional VVA treatments. We initiated the REJOICE Trial, a multicenter, double-blind, placebo-controlled phase 3 clinical trial during the third quarter of 2014 to assess the safety and efficacy of TX-004HR for the treatment of moderate to severe dyspareunia, or painful intercourse, as a symptom of VVA due to menopause. We are conducting a single 12 week study, evaluating three different doses of estradiol: 4 mcg, 10 mcg and 25 mcg versus placebo. The FDA has noted that a single, large, well-controlled clinical trial to support safety and efficacy should be sufficient to submit an NDA for TX-004HR for the proposed indication and that to support the indication in a single trial, evidence of efficacy for a given dose would need to show statistical significance of at a 0.01 level. The study has been designed to include four primary endpoints: the reduction of vaginal pH levels to less than 5.0, an increase in superficial cells, a decrease in parabasal cells and the improvement of dyspareunia. If approved, the 4 mcg formulation would represent a lower effective dose than the currently available VVA therapies approved by the FDA. The trial is designed to enroll approximately 700 patients across approximately 100 sites. The last patient was enrolled in the REJOICE Trial in June 2015, and we have completed the last patient visit in the trial.  We currently anticipate that the topline results of the trial will be reported during the fourth quarter of 2015. Based on such timeline and successful reports of the trial, we would anticipate filing an NDA for TX-004HR as soon as the first half of 2016 and that such NDA could be approved by the FDA as soon as the first quarter of 2017, assuming an FDA review period of ten months from the receipt date to the PDUFA date for a non-new molecular entity.

 

As of September 30, 2015, we had 13 issued patents, which included 11 utility patents that relate to our combination progesterone and estradiol formulations, one utility patent that relates to TX-004HR, which establishes an important intellectual property foundation for TX-004HR, and one method patent that relates to our OPERA® information technology platform.

 

Research and Development Expenses

 

A significant portion of our operating expenses to date have been incurred in research and development activities. Research and development expenses relate primarily to the discovery and development of our drug products. Our business model is dependent upon our company continuing to conduct a significant amount of research and development. Our research and development expenses consist primarily of expenses incurred under agreements with contract research organizations, or CROs, investigative sites and consultants that conduct our clinical trials and a substantial portion of our preclinical studies; employee-related expenses, which include salaries and benefits, and non-cash share-based compensation; the cost of developing our chemistry, manufacturing and controls capabilities, and acquiring clinical trial materials; and costs associated with other research activities and regulatory approvals.

 

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We make payments to the CROs based on agreed upon terms that may include payments in advance of a study starting date. Nonrefundable advance payments for goods and services that will be used in future research and development activities are expensed when the activity has been performed or when the goods have been received rather than when the payment is made. Advance payments to be expensed in future research and development activities were $948,499 at September 30, 2015, of which $755,152 was included in Other current assets and $193,347 was included in long term Prepaid expense on the accompanying consolidated balance sheets. Advance payments to be expensed in future research and development activities were $1,175,082 at December 31, 2014, of which $711,362 was included in Other current assets and $463,720 was included in long term Prepaid expense on the accompanying consolidated balance sheets.

 

The following table indicates our research and development expense by project/category for the periods indicated (in 000s):

 

    Three months ended September 30,   Nine months ended September 30,
    2015   2014   2015   2014
TX-001HR   $ 8,175     $ 11,518     $ 27,504     $ 20,320  
TX-002HR     6       85       18       1,381  
TX-004HR     4,581       567       18,242       931  
Other research and development(1)     3,660       2,739       13,025       6,420  
    $ 16,422     $ 14,909     $ 58,789     $ 29,052  

____________

(1) Product costs are classified as other research and development expenses until one of our drug products receives IND approval from the FDA.

 

Research and development expenditures will continue to be significant as we continue development of our pipeline of novel drug candidates. We expect to incur significant research and development costs as we develop our drug pipeline, complete the ongoing clinical trials of our drug candidates, conduct our ongoing phase 3 clinical trials, manufacturing, scale-up, and prepare regulatory submissions.

 

The costs of clinical trials may vary significantly over the life of a project due to factors that include but are not limited to the following: per patient trial costs, the number of patients that participate in the trials; the number of sites included in the trials; the length of time each patient is enrolled in the trial; the number of doses that patients receive; the drop-out or discontinuation rates of patients; the amount of time required to recruit patients for the trial, the duration of patient follow-up; and the efficacy and safety profile of the drug candidate. We base our estimated expenses related to clinical trials on estimates that are based on our experience and estimates from CROs and other third parties.

 

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Results of Operations

 

Three months ended September 30, 2015 compared with three months ended September 30, 2014

 

   

Three Months Ended

September 30,

   
    2015   2014   Change
    (000s)
Revenues, net   $ 5,190     $ 4,186     $ 1,004  
Cost of goods sold     1,194       1,069       125  
Operating expenses     23,499       20,965       2,534  
     Operating loss     (19,503 )     (17,848 )     (1,655 )
Total other income     31       16       15  
Net loss   $ (19,472 )   $ (17,832 )   $ (1,640 )

 

Revenues and Cost of Goods Sold

 

Revenues for the three months ended September 30, 2015 increased approximately $1,004,000, or 24%, to approximately $5,190,000, compared with approximately $4,186,000 for the three months ended September 30, 2014. Of this $1,004,000 increase, approximately $825,000, or 82%, was attributable to an increase in the number of units sold and approximately $179,000, or 18%, was attributable to product mix and an increase in the average net sales price of our products. Cost of goods sold increased approximately $125,000 or 12%, to approximately $1,194,000 for the three months ended September 30, 2015, compared with approximately $1,069,000 for the three months ended September 30, 2014. Cost of goods sold as a percentage of revenue was approximately 23% and 26% for the three months ended September 30, 2015 and 2014, respectively, which was primarily attributable to a favorable change in product mix.

 

Operating Expenses

 

Our principal operating costs include the following items as a percentage of total operating expenses.

   

 

Three Months Ended

September 30,

      2015       2014*
Research and development costs     69.9 %     71.1 %
Human resource costs, including salaries, benefits and taxes     14.7 %     12.8 %
Sales and marketing costs, excluding human resource costs     6.2 %     8.0 %
Professional fees for legal, accounting and consulting     4.8 %     3.5 %

Other operating expenses

    4.4 %     4.6 %

 

*Prior year numbers have been reclassified to conform to current year’s presentation

 

Operating expenses increased by approximately $2,534,000 or 12%, to approximately $23,499,000 for the three months ended September 30, 2015, from approximately $20,965,000 for the three months ended September 30, 2014 as a result of the following items:

 

      (000s)
Increase in research and development costs   $ 1,513  
Increase in human resource costs, including salaries, benefits and taxes     764  
Increase in professional fees for legal, accounting and consulting     396  
Increase in other operating expenses     82  
Decrease in sales and marketing, excluding human resource costs     (221 )
    $ 2,534  

 

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Research and development costs for the three months ended September 30, 2015 increased by approximately $1,513,000, or 10%, to approximately $16,422,000, compared with $14,909,000 for the three months ended September 30, 2014. Research and development costs include costs related to clinical trials as well as salaries, wages, non-cash compensation and benefits of personnel involved in research and development activities.  The increase in research and development costs was primarily due to an increase in scale-up and manufacturing activities for our phase 3 hormone therapy drug candidates, partially offset by lower clinical trial costs. Research and developments costs during the three months ended September 30, 2015 included the following research and development projects.

 

During the three months ending September 30, 2015 and the period from February 2013 (project inception) through September 30, 2015, we have incurred approximately $8,175,000 and $58,436,000, respectively, in research and development costs with respect to TX-001HR, our combination estradiol and progesterone drug candidate.

 

During the three months ended September 30, 2015 and the period April 2013 (project inception) through September 30, 2015, we have incurred approximately $6,000 and $2,520,000, respectively, in research and development costs with respect to TX-002HR, our progesterone only drug candidate.

 

During the three months ended September 30, 2015 and the period from August 2014 (project inception) through September 30, 2015, we have incurred approximately $4,581,000 and $22,225,000, respectively, in research and development costs with respect to TX-004HR, our vaginal estradiol softgel drug candidate.

 

For a discussion of the nature of efforts and steps necessary to complete these projects, see “Item 1. Business — Research and Development” in our Annual Report. For a discussion of the risks and uncertainties associated with completing development of our products, see “Item 1A. Risk Factors — Risks Related to Our Business” in our Annual Report. For a discussion of the extent and nature of additional resources that we may need to obtain if our current liquidity is not expected to be sufficient to complete these projects, see “— Liquidity and Capital Resources.” For a discussion as to whether a future milestone such as completion of a development phase, date of filing an NDA with a regulatory agency or approval from a regulatory agency can be reliably determined, see “Item 1. Business — Our Hormone Therapy Drug Candidates,” “Item 1. Business — Products in Development” and “Item 1. Business — Pharmaceutical Regulation” in our Annual Report. Future milestones, including NDA submission dates, are not easily determinable as such milestones are dependent on various factors related to our clinical trials, including the timing of ongoing patient recruitment efforts to find eligible subjects for the applicable trials.

 

Human resource costs, including salaries, benefits and taxes, for the three months ended September 30, 2015 increased by approximately $764,000, or 28%, to approximately $3,465,000, compared with $2,701,000 for the three months ended September 30, 2014, primarily as a result of increases of approximately $520,000 in non-cash compensation related to stock option awards and approximately $244,000 in personnel costs.

 

Professional fees for the three months ended September 30, 2015 increased by approximately $396,000, or 54%, to approximately $1,129,000, compared with $733,000 for the three months ended September 30, 2014, primarily as a result of higher consulting fees.

 

Other operating expense for the three months ended September 30, 2015 increased by approximately $82,000, or 9%, to approximately $1,034,000, compared with $952,000 for the three months ended September 30, 2014, primarily as a result of increased travel and rent expense.

 

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Sales and marketing costs for the three months ended September 30, 2015 decreased by approximately $221,000, or 13%, to approximately $1,448,000, compared with $1,669,000 for the three months ended September 30, 2014, as a result of decreased costs related to advertising programs.

 

Operating Loss

 

As a result of the foregoing, our operating loss increased approximately $1,655,000, or 9%, to approximately $19,503,000 for the three months ended September 30, 2015, compared with approximately $17,848,000 for the three months ended September 30, 2014, primarily as a result of increased research and development costs associated with our continued development of our hormone therapy drug candidates, partially offset by increased revenue from sales of our prenatal vitamin products.

 

As a result of the continued development of our hormone therapy drug candidates, we anticipate that we will continue to have operating losses for the near future until our hormone therapy drug candidates are approved by the FDA and brought to market, although there is no assurance that we will attain such approvals or that any marketing of our hormone therapy drug candidates, if approved, will be successful.

 

Total other income

 

Other income increased by approximately $15,000, or 94%, to approximately $31,000 for the three months ended September 30, 2015 compared with $16,000 for the comparable period in 2014.

 

Net Loss

 

As a result of the net effects of the foregoing, net loss increased approximately $1,640,000, or 9%, to approximately $19,472,000 for the three months ended September 30, 2015, compared with approximately $17,832,000 for the three months ended September 30, 2014. Net loss per share of Common Stock, basic and diluted, was $0.11 for the three months ended September 30, 2015, compared with $0.12 per share of Common Stock for the three months ended September 30, 2014.

 

Nine months ended September 30, 2015 compared with nine months ended September 30, 2014

 

   

Nine Months Ended

September 30,

   
    2015   2014   Change
    (000s)
Revenues, net   $ 14,513     $ 10,769     $ 3,744  
Cost of goods sold     3,271       2,792       479  
Operating expenses     78,923       45,703       33,220  
     Operating loss     (67,681 )     (37,726 )     (29,955 )
Other income (expense)     87       (189 )     276  
Net loss   $ (67,594 )   $ (37,915 )   $ (29,679 )

 

Revenues and Cost of Goods Sold

 

Revenues for the nine months ended September 30, 2015 increased approximately $3,744,000, or 35%, to approximately $14,513,000, compared with approximately $10,769,000 for the nine months ended September 30, 2014. Of this $3,744,000 increase, approximately $2,818,000, or 75 %, was attributable to an increase in the number of units sold and approximately $926,000, or 25%, was attributable to product mix and an increase in the average net sales price of our products. Cost of goods sold increased approximately $479,000, or 17%, to approximately $3,271,000 for the nine months ended September 30, 2015, compared with approximately $2,792,000 for the nine months ended September 30, 2014. Cost of goods sold as a percentage of revenue was approximately 23% and 26% for the nine months ended September 30, 2015 and 2014, respectively, which was primarily attributable to a favorable change in product mix.

 

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Operating Expenses

 

Our principal operating costs include the following items as a percentage of total operating expenses.

   

 

Nine Months Ended

September 30,

      2015       2014*
Research and development costs     74.5 %     63.6 %
Human resource costs, including salaries, benefits and taxes     12.2 %     17.4 %
Sales and marketing costs, excluding human resource costs     5.6 %     9.9 %
Professional fees for legal, accounting and consulting     3.9 %     3.7 %

Other operating expenses 

    3.8 %     5.4 %

 

*Prior year numbers have been reclassified to conform to current year’s presentation

 

Operating expenses increased by approximately $33,220,000 or 73%, to approximately $78,923,000 for the nine months ended September 30, 2015, from approximately $45,703,000 for the nine months ended September 30, 2014 as a result of the following items:

 

      (000s)
Increase in research and development costs   $ 29,737  
Increase in professional fees for legal, accounting and consulting     1,360  
Increase in human resource costs, including salaries, benefits and taxes     1,674  
Increase in other operating expenses     582  
Decrease in sales and marketing, excluding human resource costs     (133 )
    $ 33,220  

 

Research and development costs for the nine months ended September 30, 2015 increased by approximately $29,737,000, or 102%, to approximately $58,789,000, compared with $29,052,000 for the nine months ended September 30, 2014. Research and development costs include costs related to clinical trials as well as salaries, wages, non-cash compensation and benefits of personnel involved in research and development activities. Research and development costs increased as a direct result of the development of our hormone therapy candidates, related clinical trials and manufacturing, and scale-up. Research and developments costs during the nine months ended September 30, 2015 included the following research and development projects.

 

During the nine months ending September 30, 2015 and the period from February 2013 (project inception) through September 30, 2015, we have incurred approximately $27,504,000 and $58,436,000, respectively, in research and development costs with respect to TX-001HR, our combination estradiol and progesterone drug candidate.

 

During the nine months ended September 30, 2015 and the period April 2013 (project inception) through September 30, 2015, we have incurred approximately $18,000 and $2,520,000, respectively, in research and development costs with respect to TX-002HR, our progesterone only drug candidate.

 

During the nine months ended September 30, 2015 and the period from August 2014 (project inception) through September 30, 2015, we have incurred approximately $18,242,000 and $22,225,000, respectively, in research and development costs with respect to TX-004HR, our vaginal estradiol softgel drug candidate.

 

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For a discussion of the nature of efforts and steps necessary to complete these projects, see “Item 1. Business — Research and Development” in our Annual Report. For a discussion of the risks and uncertainties associated with completing development of our products, see “Item 1A. Risk Factors — Risks Related to Our Business” in our Annual Report. For a discussion of the extent and nature of additional resources that we may need to obtain if our current liquidity is not expected to be sufficient to complete these projects, see “— Liquidity and Capital Resources.” For a discussion as to whether a future milestone such as completion of a development phase, date of filing an NDA with a regulatory agency or approval from a regulatory agency can be reliably determined, see “Item 1. Business — Our Hormone Therapy Drug Candidates,” “Item 1. Business — Products in Development” and “Item 1. Business — Pharmaceutical Regulation” in our Annual Report. Future milestones, including NDA submission dates, are not easily determinable as such milestones are dependent on various factors related to our clinical trials, including the timing of ongoing patient recruitment efforts to find eligible subjects for the applicable trials.

 

Professional fees for the nine months ended September 30, 2015 increased by approximately $1,360,000, or 79%, to approximately $3,072,000, compared with $1,712,000 for the nine months ended September 30, 2014, as a result of higher legal, consulting, accounting and Board of Director expenses.

 

Human resource costs, including salaries, benefits and taxes, for the nine months ended September 30, 2015 increased by approximately $1,674,000, or 21%, to approximately $9,644,000, compared with $7,970,000 for the nine months ended September 30, 2014, primarily as a result of an increase of approximately $978,000 in personnel costs, and an increase of approximately $696,000 in non-cash compensation related to stock option awards.

 

Other operating expense for the nine months ended September 30, 2015 increased by approximately $582,000, or 24%, to approximately $3,035,000, compared with approximately $2,453,000 for the nine months ended September 30, 2014, primarily as a result of increases in data services and insurance expenses.

 

Sales and marketing costs for the nine months ended September 30, 2015 decreased by approximately $133,000, or 3%, to approximately $4,383,000, compared with $4,516,000 for the nine months ended September 30, 2014, as a result of decreased marketing expense following the launch of our VitaPearl and Prena1 Pearl products during the first quarter of 2014, partially offset by increased costs related to sales force incentive programs during the nine months ended September 30, 2015.

 

Operating Loss

 

As a result of the foregoing, our operating loss increased approximately $29,955,000, or 79%, to approximately $67,681,000 for the nine months ended September 30, 2015, compared with approximately $37,726,000 for the nine months ended September 30, 2014, primarily as a result of increased research and development costs associated with our continued development of our hormone therapy drug candidates, partially offset by increased revenue from sales of our prenatal vitamin products.

 

As a result of the continued development of our hormone therapy drug candidates, we anticipate that we will continue to have operating losses for the near future until our hormone therapy drug candidates are approved by the FDA and brought to market, although there is no assurance that we will attain such approvals or that any marketing of our hormone therapy drug candidates, if approved, will be successful.

 

Total other income (expense)

 

Total other income (expense) changed by approximately $276,000, or 146%, to non-operating income of approximately $87,000 for the nine months ended September 30, 2015 compared with an expense of approximately $189,000 for the comparable period in 2014. This change was primarily a result of the elimination of financing costs for the nine months ended September 30, 2015.

 

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Net Loss

 

As a result of the net effects of the foregoing, net loss increased approximately $29,679,000, or 78%, to approximately $67,594,000 for the nine months ended September 30, 2015, compared with approximately $37,915,000 for the nine months ended September 30, 2014. Net loss per share of Common Stock, basic and diluted, was $0.39 for the nine months ended September 30, 2015, compared with $0.26 per share of Common Stock for the nine months ended September 30, 2014.

 

Liquidity and Capital Resources

 

We have funded our operations primarily through public offerings of our Common Stock and the private placement of equity and debt securities. For the years ending December 31, 2014 and 2013, we received approximately $43 million and $79 million in net proceeds, respectively, from the issuance of shares of our Common Stock. During the nine months ended September 30, 2015, we received approximately $91 million in net proceeds from the issuance of shares of our Common Stock. As of September 30, 2015, we had cash and cash equivalents totaling approximately $81 million, however, changing circumstances may cause us to consume funds significantly faster than we currently anticipate, and we may need to spend more money than currently expected because of circumstances beyond our control.

 

On July 9, 2015, we entered into an underwriting agreement with Stifel, Nicolaus & Company, Incorporated and Guggenheim Securities, LLC, as the representatives of the several underwriters, or the Stifel Underwriters, relating to an underwritten public offering of 3,846,154 shares of Common Stock at a public offering price of $7.80 per share. Under the terms of the underwriting agreement, we granted the Stifel Underwriters a 30-day option to purchase up to an aggregate of 576,923 additional shares of Common Stock, which option was exercised in full. The net proceeds to us from the offering were approximately $32.2 million, after deducting underwriting discounts and commissions and other estimated offering expenses payable by us. The offering closed on July 15, 2015 and we issued 4,423,077 shares of our Common Stock.

 

On February 10, 2015, we entered into an underwriting agreement, or the Cowen Agreement, with Cowen and Company, LLC, as the representative of the several underwriters, or the Cowen Underwriters, relating to an underwritten public offering of 13,580,246 shares of Common Stock, at a public offering price of $4.05 per share. Under the terms of the Cowen Agreement, we granted the Cowen Underwriters a 30-day option to purchase up to an aggregate of 2,037,036 additional shares of Common Stock, which option was exercised in full. The net proceeds to us from the offering were approximately $59.1 million, after deducting underwriting discounts and commissions and other estimated offering expenses payable by us. The offering closed on February 17, 2015 and we issued 15,617,282 shares of our Common Stock.

 

We believe that our existing cash will allow us to fund our operating plan through at least the next 12 months. If our available cash is insufficient to satisfy our liquidity requirements, we may seek to sell additional equity or debt securities or obtain a credit facility. Debt financing, if available, may involve agreements that include covenants limiting or restricting our ability to take specific actions, such as incurring additional debt, making capital expenditures, or declaring dividends. To the extent that we raise additional capital through the sale of equity or convertible debt securities, the ownership interest of our existing shareholders will be diluted, and the terms of these new securities may include liquidation or other preferences that adversely affect the rights of our existing stockholders. If we raise additional funds through collaborations, strategic alliances, or licensing arrangements with third parties, we may have to relinquish valuable rights to our technologies, future revenue streams, research programs, or proposed products. Additionally, we may have to grant licenses on terms that may not be favorable to us.

 

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We need substantial amounts of cash to complete the clinical development of our hormone therapy drug candidates. The following table sets forth the primary sources and uses of cash for each of the periods set forth below:

 

Summary of (Uses) and Sources of Cash

 

   

Nine Months Ended

September 30,

    2015   2014
      (000)
Net cash used in operating activities   $ (62,434 )   $ (30,236 )
Net cash used in investing activities   $ (134 )   $ (224 )
Net cash provided by financing activities   $ 92,330     $ 43,268  

 Operating Activities

 

The use of cash in both periods resulted primarily from our net loss adjusted for non-cash charges and changes in components of working capital. The increase of approximately $32,198,000 in cash used in operating activities for the nine months ended September 30, 2015 compared with the comparable period in the prior year was due primarily to increased research and development, and sales, general, and administrative costs. These were partially offset by an increase of approximately $3,744,000 in revenue over the same periods.

 

Investing Activities

 

A reduction in spending on patent and trademarks and property and equipment resulted in a minor decrease in cash used in investing activities for the nine months ended September 30, 2015 compared with the same period in 2014.

 

Financing Activities

 

Financing activities represent the principal source of our cash flow. Our financing activities for the nine months ended September 30, 2015 consisted of the proceeds from the February 2015 and July 2015 underwritten public offering of our Common Stock and stock option and warrant exercises.

 

Contractual Obligations

 

On February 18, 2015, we entered into an agreement to lease additional administrative office space in Boca Raton, Florida, pursuant to an addendum to our existing 63 month non-cancelable operating lease that commenced on July 1, 2013 and expires on September 30, 2018. This addendum became effective April 1, 2015 and will expire with the original lease term on September 30, 2018. The lease addendum stipulates, among other things, average base monthly rents of $9,367 (inclusive of estimated operating expenses) and sales tax, for total minimum payments over the life of the lease of $393,429.

 

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New Accounting Pronouncements

 

Recently Issued Accounting Pronouncements

 

In July 2015, the Financial Accounting Standards Board, or FASB, issued final guidance that requires entities to measure inventory at the lower of cost or net realizable value rather than at the lower of cost or market (LOCOM). The guidance applies only to inventories for which cost is determined by methods other than last-in first-out (LIFO) or the retail inventory method (RIM). Entities that use LIFO or RIM will continue to use existing impairment models. The new guidance does not change the calculation of Entities already calculate net realizable value that entities are required to calculate when applying today’s existing LOCOM guidance, and the new guidance doesn’t change that calculation. Net realizable value is the estimated selling price in the ordinary course of business, less reasonably predictable costs of completion, disposal and transportation. Under the new guidance, however, entities will no longer need to calculate other measures of “market.” The guidance is effective for public business entities for fiscal years beginning after December 15, 2016, and interim periods within those fiscal years. Early adoption is permitted. We are currently evaluating the impact of this guidance on our consolidated financial statements and disclosures.

 

In June 2015 the FASB issued Accounting Standards Update, or ASU, Technical Corrections and Improvements, No. 2015-10, to correct differences between original guidance and the Accounting Standards Codification, or ASC, clarify the guidance, correct references and make minor improvements affecting a variety of topics. Amendments that the FASB deemed more substantive are effective for fiscal years, and interim periods within those fiscal years, beginning after December 15, 2015. The other amendments are effective immediately. We do not expect the adoption of ASU 2015-10 to have a material effect on our consolidated financial statements and disclosures.

 

In August 2014, the FASB issued ASU No. 2014-15, Presentation of Financial Statements-Going Concern (Subtopic 205-40): Disclosure of Uncertainties about an Entity’s Ability to Continue as a Going Concern. ASU 2014-15 requires management to evaluate whether there are conditions and events that raise substantial doubt about the entity’s ability to continue as a going concern within one year after the financial statements are issued (or available to be issued when applicable) and, if so, disclose that fact. ASU 2014-15 is effective for annual periods ending after December 15, 2016 and interim periods within annual periods beginning after December 15, 2016. Early adoption is permitted for annual or interim reporting periods for which the financial statements have not previously been issued. We do not expect the adoption of ASU 2014-15 to have a material effect on our consolidated financial statements and disclosures.

 

In May 2014, the FASB and the International Accounting Standards Board (IASB) issued ASU No. 2014-09, Revenue from Contracts with Customers (Topic 606). The standard’s core principle is that a company will recognize revenue when it transfers promised goods or services to customers in an amount that reflects the consideration to which the company expects to be entitled in exchange for those goods or services. In doing so, companies will need to use more judgment and make more estimates than under previous guidance. These may include identifying performance obligations in the contract, estimating the amount of variable consideration to include in the transaction price and allocating the transaction price to each separate performance obligations. In July 2015, the FASB approved the proposal to defer the effective date of ASU 2014-09 standard by one year. Early adoption is permitted after December 15, 2016, and the standard is effective for public entities for annual reporting periods beginning after December 15, 2017 and interim periods therein. We are currently evaluating the impact of ASU 2014-09 on our consolidated financial statements and disclosures.

 

We do not believe there would have been a material effect on the accompanying consolidated financial statements had any other recently issued, but not yet effective, accounting standards been adopted in the current period.

 

Critical Accounting Policies

The accompanying unaudited interim consolidated financial statements are prepared in conformity with accounting principles generally accepted in the United States. As such, we are required to make certain estimates, judgments and assumptions that we believe are reasonable based upon the information available. These estimates and assumptions affect the reported amounts of assets and liabilities as of the date of the financial statements and the reported amounts of revenue and expenses during the reporting period. We routinely evaluate our estimates based on historical experience and on various other assumptions that management believes are reasonable under the circumstances. Actual results may differ from these estimates under different assumptions or conditions. During the three months ended September 30, 2015, we did not experience any significant changes in estimates or judgments inherent in the preparation of our consolidated financial statements. A summary of our significant accounting policies is contained in Note 2 to our consolidated financial statements included in our Annual Report on Form 10-K for the year ended December 31, 2014 and Note 3 of our unaudited interim consolidated financial statements included in this Quarterly Report on Form 10-Q for the quarterly period ended September 30, 2015.

Item 3. Quantitative and Qualitative Disclosures about Market Risk

 

Our market risk has not changed materially from the interest rate risk disclosed in Item 7A of our Annual Report.

 

30 
 

Item 4. Controls and Procedures

 

Disclosure Controls and Procedures

 

Disclosure controls and procedures are designed to ensure that information required to be disclosed in the reports filed or submitted under the Securities Exchange Act of 1934, as amended, or the Exchange Act, is recorded, processed, summarized and reported, within the time period specified in the SEC's rules and forms and is accumulated and communicated to our principal executive officer and principal financial officer, as appropriate, in order to allow timely decisions in connection with required disclosure.

Evaluation of Disclosure Controls and Procedures

 

Our management, with the participation of our Chief Executive Officer and Chief Financial Officer, evaluated the effectiveness of our disclosure controls and procedures (as defined in Rules 13a-15(e) and 15d-15(e) under the Exchange Act) as of the end of the period covered by this Quarterly Report on Form 10-Q. Based on that evaluation, our Chief Executive Officer and Chief Financial Officer concluded that our disclosure controls and procedures as of the end of the period covered by this Quarterly Report on Form 10-Q were effective in providing reasonable assurance that information required to be disclosed by us in reports that we file or submit under the Exchange Act is (i) recorded, processed, summarized and reported within the time periods specified in the SEC’s rules and forms and (ii) accumulated and communicated to our management, including our Chief Executive Officer and Chief Financial Officer, as appropriate, to allow timely decisions regarding required disclosure.

 

Our management, including our Chief Executive Officer and Chief Financial Officer, does not expect that our disclosure controls and procedures or our internal controls will prevent all error and all fraud. A control system, no matter how well conceived and operated, can provide only reasonable, not absolute, assurance that the objectives of the control system are met. Further, the design of a control system must reflect the fact that there are resource constraints, and the benefits of controls must be considered relative to their costs. Because of the inherent limitations in all control systems, no evaluation of controls can provide absolute assurance that all control issues, misstatements, errors, and instances of fraud, if any, within our company have been or will be prevented or detected. Further, internal controls may become inadequate as a result of changes in conditions, or through the deterioration of the degree of compliance with policies or procedures.

 

Changes in Internal Controls

 

During the three months ended September 30, 2015, there were no changes in our internal control over financial reporting that have materially affected, or are reasonably likely to materially affect, our internal control over financial reporting.

 

PART II - OTHER INFORMATION

 

Item 1. Legal Proceedings

 

From time to time, we are involved in litigation and proceedings in the ordinary course of our business. We are not currently involved in any legal proceeding that we believe would have a material adverse effect on our business or financial condition.

 

Item 1A. Risk Factors

 

There have been no material changes to the risk factors previously disclosed in our Annual Report.

 

31 
 

Item 2. Unregistered Sales of Equity Securities and Use of Proceeds

On August 7, 2015, we issued 80,635 shares of Common Stock, pursuant to the warrant cashless exercise provision, upon the exercise of warrants previously issued to an outside service provider. On July 29, 2015, we issued 151,562 shares of Common Stock, pursuant to the warrant cashless exercise provision, upon the exercise of warrants previously issued to an outside party. The shares of Common Stock were issued in reliance on the exemption from registration provided by Section 4(a)(2) of the Securities Act of 1933, as amended.

 

Item 6. Exhibits

  

Exhibit   Date   Description
1.1   July 9, 2015   Underwriting Agreement, dated July 9, 2015, between the Company and Stifel, Nicolaus & Company, Incorporated and Guggenheim Securities, LLC, as the representatives of the several underwriters named in Schedule A thereto (previously filed as Exhibit 1.1 to the Current Report on Form 8-K filed by the Company with the SEC on July 15, 2015 and incorporated herein by reference).
31.1*   November 5, 2015   Certification of Chief Executive Officer pursuant to Rule 13a-14(a) and Rule 15d-14(a)
31.2*   November 5, 2015   Certification of Chief Financial Officer pursuant to Rule 13a-14(a) and Rule 15d-14(a)
32.1*   November 5, 2015   Section 1350 Certification of Chief Executive Officer
32.2*   November 5, 2015   Section 1350 Certification of Chief Financial Officer
101.INS*   n/a   XBRL Instance Document
101.SCH*   n/a   XBRL Taxonomy Extension Schema Document
101.CAL*   n/a   XBRL Taxonomy Extension Calculation Linkbase Document
101.DEF*   n/a   XBRL Taxonomy Extension Definition Linkbase Instance Document
101.LAB*   n/a   XBRL Taxonomy Extension Label Linkbase Instance Document
101.PRE*   n/a   XBRL Taxonomy Extension Presentation Linkbase Instance Document

 

____________________________

* Filed herewith.

 

32 
 

 

SIGNATURES

 

Pursuant to the requirements of the Securities Exchange Act of 1934, the Company has duly caused this report to be signed on its behalf by the undersigned thereunto duly authorized.

 

DATE: November 5, 2015

 

  THERAPEUTICSMD, INC.
     
  By: /s/ Robert G. Finizio
    Robert G. Finizio
    Chief Executive Officer
    (Principal Executive Officer)
     
  By: /s/ Daniel A. Cartwright
    Daniel A. Cartwright
    Chief Financial Officer
    (Principal Financial and Accounting Officer)

 

 

33

 

 

EX-31.1 2 ex31-1.htm CERTIFICATION OF THE CHIEF EXECUTIVE OFFICER

 

TherapeuticsMD, Inc. 10-Q  

Exhibit 31.1

 

CERTIFICATION OF CHIEF EXECUTIVE OFFICER

 

I, Robert G. Finizio, certify that:

 

(1) I have reviewed this quarterly report on Form 10-Q of TherapeuticsMD, Inc.;

 

(2) Based on my knowledge, this report does not contain any untrue statement of a material fact or omit to state a material fact necessary to make the statements made, in light of the circumstances under which such statements were made, not misleading with respect to the period covered by this report;

 

(3) Based on my knowledge, the financial statements, and other financial information included in this report, fairly present in all material respects the financial condition, results of operations and cash flows of the registrant as of, and for, the periods presented in this report;

 

(4) The registrant's other certifying officer and I are responsible for establishing and maintaining disclosure controls and procedures (as defined in Exchange Act Rules 13a-15(e) and 15d-15(e)) and internal control over financial reporting (as defined in Exchange Act Rules 13a-15(f) and 15d-15(f)) for the registrant and have:

 

  (a) Designed such disclosure controls and procedures, or caused such disclosure controls and procedures to be designed under our supervision, to ensure that material information relating to the registrant, including its consolidated subsidiaries, is made known to us by others within those entities, particularly during the period in which this report is being prepared;
  (b) Designed such internal control over financial reporting, or caused such internal control over financial reporting to be designed under our supervision, to provide reasonable assurance regarding the reliability of financial reporting and the preparation of financial statements for external purposes in accordance with generally accepted accounting principles;
  (c) Evaluated the effectiveness of the registrant’s disclosure controls and procedures and presented in this report our conclusions about the effectiveness of the disclosure controls and procedures, as of the end of the period covered by this report based on such evaluation; and
  (d) Disclosed in this report any change in the registrant’s internal control over financial reporting that occurred during the registrant’s most recent fiscal quarter (the registrant’s fourth fiscal quarter in the case of an annual report) that has materially affected, or is reasonably likely to materially affect, the registrant’s internal control over financial reporting; and

 

(5) The registrant's other certifying officer and I have disclosed, based on our most recent evaluation of internal control over financial reporting, to the registrant’s auditors and the audit committee of the registrant’s board of directors (or persons performing the equivalent functions):

 

  (a) All significant deficiencies and material weaknesses in the design or operation of internal control over financial reporting which are reasonably likely to adversely affect the registrant’s ability to record, process, summarize and report financial information; and
  (b) Any fraud, whether or not material, that involves management or other employees who have a significant role in the registrant’s internal control over financial reporting.

 

November 5, 2015   /s/ Robert G. Finizio
    Robert G. Finizio
    Chief Executive Officer
(Principal Executive Officer)

 

 

 

 

EX-31.2 3 ex31-2.htm CERTIFICATION OF THE CHIEF FINANCIAL OFFICER

 

TherapeuticsMD, Inc. 10-Q 

Exhibit 31.2

 

CERTIFICATION OF CHIEF FINANCIAL OFFICER

 

I, Daniel A. Cartwright, certify that:

 

(1) I have reviewed this quarterly report on Form 10-Q of TherapeuticsMD, Inc.;

 

(2) Based on my knowledge, this report does not contain any untrue statement of a material fact or omit to state a material fact necessary to make the statements made, in light of the circumstances under which such statements were made, not misleading with respect to the period covered by this report;

 

(3) Based on my knowledge, the financial statements, and other financial information included in this report, fairly present in all material respects the financial condition, results of operations and cash flows of the registrant as of, and for, the periods presented in this report;

 

(4) The registrant's other certifying officer and I are responsible for establishing and maintaining disclosure controls and procedures (as defined in Exchange Act Rules 13a-15(e) and 15d-15(e)) and internal control over financial reporting (as defined in Exchange Act Rules 13a-15(f) and 15d-15(f)) for the registrant and have:

 

  (a) Designed such disclosure controls and procedures, or caused such disclosure controls and procedures to be designed under our supervision, to ensure that material information relating to the registrant, including its consolidated subsidiaries, is made known to us by others within those entities, particularly during the period in which this report is being prepared;
  (b) Designed such internal control over financial reporting, or caused such internal control over financial reporting to be designed under our supervision, to provide reasonable assurance regarding the reliability of financial reporting and the preparation of financial statements for external purposes in accordance with generally accepted accounting principles;
  (c) Evaluated the effectiveness of the registrant’s disclosure controls and procedures and presented in this report our conclusions about the effectiveness of the disclosure controls and procedures, as of the end of the period covered by this report based on such evaluation; and
  (d) Disclosed in this report any change in the registrant’s internal control over financial reporting that occurred during the registrant’s most recent fiscal quarter (the registrant’s fourth fiscal quarter in the case of an annual report) that has materially affected, or is reasonably likely to materially affect, the registrant’s internal control over financial reporting; and

 

(5) The registrant's other certifying officer and I have disclosed, based on our most recent evaluation of internal control over financial reporting, to the registrant’s auditors and the audit committee of the registrant’s board of directors (or persons performing the equivalent functions):

 

  (a) All significant deficiencies and material weaknesses in the design or operation of internal control over financial reporting which are reasonably likely to adversely affect the registrant’s ability to record, process, summarize and report financial information; and
  (b) Any fraud, whether or not material, that involves management or other employees who have a significant role in the registrant’s internal control over financial reporting.

 

November 5, 2015   /s/ Daniel A. Cartwright
    Daniel A. Cartwright
    Chief Financial Officer
(Principal Financial and Accounting Officer)

 

  

 

EX-32.1 4 ex32-1.htm CERTIFICATION OF THE CHIEF EXECUTIVE OFFICER

 

 TherapeuticsMD, Inc. 10-Q

Exhibit 32.1

 

 

SECTION 1350 CERTIFICATION OF CHIEF EXECUTIVE OFFICER

 

In connection with the quarterly report of TherapeuticsMD, Inc. (the “Company”) on Form 10-Q for the quarterly period ended September 30, 2015 as filed with the Securities and Exchange Commission on the date hereof (the “Report”), I, Robert G. Finizio, Chief Executive Officer of the Company, certify, to my best knowledge and belief, pursuant to 18 U.S.C. § 1350, as adopted pursuant to § 906 of the Sarbanes-Oxley Act of 2002, that:

 

  (1) The Report fully complies with the requirements of Section 13(a) or 15(d) of the Securities Exchange Act of 1934 (15 U.S.C. 78m(a) or 78o(d)); and
     
  (2) The information contained in the Report fairly presents, in all material respects, the financial condition and result of operations of the Company.

 

November 5, 2015   /s/ Robert G. Finizio
    Robert G. Finizio
    Chief Executive Officer

 

A signed original of this certification has been provided to the Company and will be retained by the Company and furnished to the Securities and Exchange Commission or its staff upon request.

 

 

 

 

 

EX-32.2 5 ex32-2.htm CERTIFICATION OF THE CHIEF FINANCIAL OFFICER

 

TherapeuticsMD, Inc. 10-Q 

Exhibit 32.2

 

SECTION 1350 CERTIFICATION OF CHIEF FINANCIAL OFFICER

 

In connection with the quarterly report of TherapeuticsMD, Inc. (the “Company”) on Form 10-Q for the quarterly period ended September 30, 2015 as filed with the Securities and Exchange Commission on the date hereof (the “Report”), I, Daniel A. Cartwright, Chief Financial Officer of the Company, certify to my best knowledge and belief, pursuant to 18 U.S.C. § 1350, as adopted pursuant to § 906 of the Sarbanes-Oxley Act of 2002, that:

 

(1) The Report fully complies with the requirements of Section 13(a) or 15(d) of the Securities Exchange Act of 1934 (15 U.S.C. 78m(a) or 78o(d)); and
     
  (2) The information contained in the Report fairly presents, in all material respects, the financial condition and result of operations of the Company.

 

November 5, 2015   /s/ Daniel A. Cartwright
    Daniel A. Cartwright
    Chief Financial Officer

 

A signed original of this certification has been provided to the Company and will be retained by the Company and furnished to the Securities and Exchange Commission or its staff upon request.

 

 

 

 

 

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Dec. 31, 2014
Finite-Lived Intangible Assets    
Accumulated Amortization $ (135,936) $ (113,640)
Indefinite-Lived Intangible Assets    
Gross Carrying Amount 1,460,220 1,342,228
Net Amount 1,324,284 1,228,588
Hormone therapy drug candidate patents - Pending [Member]    
Indefinite-Lived Intangible Assets    
Gross Carrying Amount 585,241 675,982
Net Amount 585,241 675,982
Multiple trademarks for vitamins/supplements [Member]    
Indefinite-Lived Intangible Assets    
Gross Carrying Amount 145,783 103,368
Net Amount 145,783 103,368
OPERA software patent [Member]    
Finite-Lived Intangible Assets    
Gross Carrying Amount 31,951 31,951
Accumulated Amortization (3,994) (2,496)
Net Amount $ 27,957 $ 29,455
Weighted Average Amortization Period 14 years 14 years 9 months
Development costs for corporate website [Member]    
Finite-Lived Intangible Assets    
Gross Carrying Amount $ 91,743 $ 91,743
Accumulated Amortization $ (91,743) $ (91,743)
Net Amount
Approved Hormone Therapy Drug Candidate Patents [Member]    
Finite-Lived Intangible Assets    
Gross Carrying Amount $ 605,502 $ 439,184
Accumulated Amortization (40,199) (19,401)
Net Amount $ 565,303 $ 419,783
Weighted Average Amortization Period   18 years
Non-Amortizing Intangible Assets [Member]    
Finite-Lived Intangible Assets    
Weighted Average Amortization Period 17 years 2 months 30 days  
XML 13 R48.htm IDEA: XBRL DOCUMENT v3.3.0.814
RELATED PARTIES (Details Narrative) - Pernix Therapeutics LLC [Member] - USD ($)
Sep. 30, 2015
Dec. 31, 2014
Receivables- legal fee reimbursement $ 250,000 $ 250,000
Payable - related party $ 46,000 $ 46,000
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STOCKHOLDERS' EQUITY (Details) - Stock Options [Member]
9 Months Ended
Sep. 30, 2015
Sep. 30, 2014
Share-based Compensation Arrangement by Share-based Payment Award [Line Items]    
Expected dividend yield 0.00% 0.00%
Minimum [Member]    
Share-based Compensation Arrangement by Share-based Payment Award [Line Items]    
Risk-free interest rate 1.47% 1.68%
Expected Volatility 58.77% 69.15%
Expected term 5 years 3 months 8 days 5 years
Maximum [Member]    
Share-based Compensation Arrangement by Share-based Payment Award [Line Items]    
Risk-free interest rate 1.54% 1.77%
Expected Volatility 62.94% 70.93%
Expected term 6 years 2 months 30 days 6 years 2 months 30 days
XML 16 R33.htm IDEA: XBRL DOCUMENT v3.3.0.814
INVENTORY (Details) - USD ($)
Sep. 30, 2015
Dec. 31, 2014
Inventory    
Finished product $ 787,232 $ 874,294
Raw material $ 82,827 155,341
Deferred costs 152,478
TOTAL INVENTORY $ 870,059 $ 1,182,113
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FIXED ASSETS, NET (Tables)
9 Months Ended
Sep. 30, 2015
Property, Plant and Equipment [Abstract]  
Schedule of fixed assets

Fixed assets, net consist of the following:

  

September 30,

2015

 

December 31,

2014

Equipment  $132,150   $132,150 
Furniture and fixtures   69,454    53,895 
    201,604    186,045 
Accumulated depreciation   (144,856)   (122,752)
     TOTAL FIXED ASSETS, NET  $56,748   $63,293 
XML 19 R50.htm IDEA: XBRL DOCUMENT v3.3.0.814
COMMITMENTS AND CONTINGENCIES (Details Narrative) - USD ($)
3 Months Ended 9 Months Ended
Sep. 30, 2015
Sep. 30, 2014
Sep. 30, 2015
Sep. 30, 2014
Commitments and Contingencies Disclosure [Abstract]        
Non-cancelable operating lease term     63 months  
Rental Expense $ 119,000 $ 90,000 $ 328,000 $ 271,000
Rental income   $ 6,000   $ 42,000
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NET LOSS PER SHARE (Details) - shares
9 Months Ended
Sep. 30, 2015
Sep. 30, 2014
Antidilutive Securities Excluded from Computation of Earnings Per Share [Line Items]    
Anti-dilutive shares excluded from earnings per share calculation 30,136,673 30,779,859
Stock Option [Member]    
Antidilutive Securities Excluded from Computation of Earnings Per Share [Line Items]    
Anti-dilutive shares excluded from earnings per share calculation 17,414,242 16,851,943
Warrants [Member]    
Antidilutive Securities Excluded from Computation of Earnings Per Share [Line Items]    
Anti-dilutive shares excluded from earnings per share calculation 12,722,431 13,927,916

XML 22 R37.htm IDEA: XBRL DOCUMENT v3.3.0.814
PREPAID EXPENSE (Details) - USD ($)
Sep. 30, 2015
Dec. 31, 2014
Prepaid Expense and Other Assets [Abstract]    
Prepaid manufacturing costs $ 978,704 $ 963,543
Prepaid research and development costs 193,347 463,720
TOTAL PREPAID EXPENSE $ 1,172,051 $ 1,427,263
XML 23 R52.htm IDEA: XBRL DOCUMENT v3.3.0.814
SUBSEQUENT EVENTS (Details Narative)
Oct. 31, 2015
Sep. 30, 2015
Number of patents   13
Subsequent Event [Member]    
Number of patents 1,750  
Number of sites 100  
XML 24 R47.htm IDEA: XBRL DOCUMENT v3.3.0.814
STOCKHOLDERS' EQUITY (Details 1) - USD ($)
3 Months Ended 9 Months Ended
Sep. 30, 2015
Sep. 30, 2015
Sep. 30, 2014
Number Options      
Options outstanding, beginning   16,792,443  
Options Granted   1,231,000 50,000
Options Exercised (95,000) (472,867) (793,800)
Options Cancelled   (136,334)  
Options outstanding, ending 17,414,242 17,414,242  
Vested and exercisable 13,848,923 13,848,923  
Weighted Average Exercise Price      
Options outstanding, beginning   $ 1.88  
Granted   6.38  
Exercised   1.25  
Cancelled   3.01  
Options outstanding, ending $ 2.21 2.21  
Vested and exercisable $ 1.59 $ 1.59  
Weighted Average Remaining Contractual Life      
Options outstanding, beginning   6 years 11 months 1 day  
Options outstanding, ending   6 years 1 month 2 days  
Vested and exercisable   5 years 5 months 27 days  
Aggregate Intrinsic Value      
Options outstanding, beginning   $ 43,996,311  
Options outstanding, ending $ 64,265,785 64,265,785  
Vested and exercisable $ 59,095,453 $ 59,095,453  
XML 25 R9.htm IDEA: XBRL DOCUMENT v3.3.0.814
INVENTORY
9 Months Ended
Sep. 30, 2015
Inventory Disclosure [Abstract]  
INVENTORY

NOTE 4 – INVENTORY

 

Inventory consists of the following:

 

  

September 30,

2015

 

December 31,

2014

Finished product  $787,232   $874,294 
Raw material   82,827    155,341 
Deferred costs   —      152,478 
     TOTAL INVENTORY  $870,059   $1,182,113 
XML 26 R43.htm IDEA: XBRL DOCUMENT v3.3.0.814
STOCKHOLDERS' EQUITY (Details Narrative) - USD ($)
3 Months Ended 9 Months Ended
Jul. 15, 2015
Jul. 09, 2015
Feb. 17, 2015
Feb. 10, 2015
Aug. 04, 2014
Jul. 29, 2014
Sep. 30, 2015
Sep. 30, 2015
Sep. 30, 2014
Dec. 31, 2014
Preferred stock, shares authorized             10,000,000 10,000,000   10,000,000
Preferred stock, par value (in dollars per share)             $ 0.001 $ 0.001   $ 0.001
Common stock, shares authorized             350,000,000 350,000,000   250,000,000
Common stock, shares issued             177,787,927 177,787,927   156,097,019
Common stock, shares outstanding             177,787,927 177,787,927   156,097,019
Number of common stock issued during period for stock options exercised             95,000 472,867 793,800  
Value of common stock issued during period for stock options exercised             $ 98,478 $ 589,867    
Share based compensation options grants in period               1,231,000 50,000  
Options exercised 1 [Member]                    
Number of common stock issued during period for stock options exercised                 674,800  
Value of common stock issued during period for stock options exercised                 $ 315,546  
Options exercised 2 [Member]                    
Common stock, shares issued                 113,837  
Number of common stock issued during period for stock options exercised                 119,607  
Stifel Underwriters [Member]                    
Number of shares issued during the period 4,423,077 3,846,154                
Share price (in dollars per share)   $ 7.80                
Number of shares issued during the period,value   $ 3,200,000                
Number of common stock issued during period for stock options exercised   576,923                
Cowen and Company, LLC (Underwriters) [Member]                    
Number of shares issued during the period     15,617,282 13,580,246            
Share price (in dollars per share)       $ 4.05            
Number of shares issued during the period,value       $ 59,100,000            
Number of common stock issued during period for stock options exercised       2,037,036            
Goldman Sachs Underwriters [Member]                    
Number of shares issued during the period         9,850,106 8,565,310        
Share price (in dollars per share)           $ 4.67        
Number of shares issued during the period,value           $ 42,800,000        
Number of common stock issued during period for stock options exercised           1,284,796        
XML 27 R29.htm IDEA: XBRL DOCUMENT v3.3.0.814
NET LOSS PER SHARE (Tables)
9 Months Ended
Sep. 30, 2015
Net Loss Per Share Tables  
Schedule of potentially dilutive securities

The table below presents the potentially dilutive securities that would have been included in our calculation of diluted net loss per share allocable to common stockholders if they were not antidilutive for the periods presented.

 

   As of September 30,
   2015  2014
Stock options   17,414,242    16,851,943 
Warrants   12,722,431    13,927,916 
    30,136,673    30,779,859 

 

XML 28 R28.htm IDEA: XBRL DOCUMENT v3.3.0.814
OTHER CURRENT LIABILITIES (Tables)
9 Months Ended
Sep. 30, 2015
Other Liabilities Disclosure [Abstract]  
Schedule of other current liabilities

Other current liabilities consist of the following:

  

September 30,

2015

 

December 31,

2014

Accrued clinical trial costs  $3,528,061   $1,706,542 
Accrued payroll, bonuses and commission costs   930,913    814,205 
Accrued legal and accounting expense   615,946    276,470 
Accrued compensated absences   490,170    442,430 
Other accrued expenses   388,268    185,965 
Allowance for coupons and returns   208,361    90,446 
Allowance for wholesale distributor fees   96,440    160,503 
Accrued rent   86,998    91,368 
Accrued royalties   41,620    72,710 
     TOTAL OTHER CURRENT LIABILITIES  $6,386,777   $3,840,639 
XML 29 R44.htm IDEA: XBRL DOCUMENT v3.3.0.814
STOCKHOLDERS' EQUITY (Details Narrative 1) - USD ($)
1 Months Ended 3 Months Ended 9 Months Ended
Jun. 30, 2013
May. 11, 2013
May. 31, 2013
Jan. 31, 2013
Sep. 30, 2015
Sep. 30, 2014
Sep. 30, 2015
Sep. 30, 2014
Warrants:                
Warrants outstanding         $ 12,772,431   $ 12,772,431  
Exercise price of warrants (in dollars per share)         $ 1.93   $ 1.93  
Other current assets         $ 755,152   $ 755,152  
Options Granted             1,231,000 50,000
Sancilio and Company Warrants [Member]                
Warrants:                
Weighted-average contractual remaining life             1 year 9 months  
Exercise price of warrants (in dollars per share)     $ 2.01          
Unamortized costs of warrants             $ 567,000  
Number of shares purchased     850,000          
Number of shares purchased forfeit     833,000          
Sancilio &amp;amp; Company Warrants 1st Installments [Member]                
Warrants:                
Number of shares purchased   283,333            
Vesting date of warrants   Jun. 30, 2013            
Fair value of warrants $ 405,066              
Expected term 5 years              
Volatility rate 45.89%              
Risk free rate 1.12%              
Dividend yield 0.00%              
Valuation method of warrants Black-Scholes Model              
Non-cash compensation recognised $ 405,066              
Sancilio and Company Warrants 2nd Installments [Member]                
Warrants:                
Number of shares purchased 283,333              
Fair value of warrants $ 462,196              
Expected term 5 years              
Volatility rate 45.84%              
Risk free rate 1.41%              
Dividend yield 0.00%              
Non-cash compensation recognised         38,517 $ 38,517 115,551 $ 115,551
Other current assets         $ 115,543   $ 115,543  
Sancilio and Company Warrants 3rd Installments [Member]                
Warrants:                
Number of shares purchased         283,334   283,334  
Outside Consultant Warrants [Member]                
Warrants:                
Weighted-average contractual remaining life             1 year 11 months 1 day  
Exercise price of warrants (in dollars per share)         $ 6.35   $ 6.35  
Expiration date of warrants             Apr. 06, 2020  
Non-cash compensation recognised         $ 42,266   $ 86,008  
Options Granted             50,000  
Multiple Advance Revolving Credit Note (Plato Warrant) [Member]                
Warrants:                
Exercise price of warrants (in dollars per share)       $ 3.20        
Number of shares purchased       1,250,000        
Expiration date of warrants       Jan. 31, 2019        
Vesting date of warrants       Oct. 31, 2013        
Fair value of warrants       $ 1,711,956        
Expected term       6 years        
Volatility rate       44.29%        
Risk free rate       0.88%        
Dividend yield       0.00%        
Amortization deferred financing costs             $ 0 $ 260,027
XML 30 R30.htm IDEA: XBRL DOCUMENT v3.3.0.814
STOCKHOLDERS' EQUITY (Tables)
9 Months Ended
Sep. 30, 2015
Stockholders' Equity Note [Abstract]  
Schedule of assumptions used in the Black-Scholes Model of stock options

The assumptions used in the Black-Scholes Model during the nine months ended September 30, 2015 and 2014 are set forth in the table below.

 

   Nine Months Ended September 30,
   2015  2014
Risk-free interest rate   1.47-1.54%   1.68-1.77%
Volatility   58.77-62.94%   69.15-70.93%
Term (in years)   5.27-6.25    5-6.25 
Dividend yield   0.00%   0.00%
Schedule of option activity

A summary of activity under the 2009 and 2012 Plans and related information follows:

 

    Number of Shares Underlying Stock Options  

 

Weighted Average Exercise Price

 

Weighted Average

Remaining

Contractual

Life in Years

 

 

 

Aggregate Intrinsic Value

Balance at December 31, 2014     16,792,443     $ 1.88       6.92     $ 43,996,311  
   Granted     1,231,000     $ 6.38                  
   Exercised     (472,867 )   $ 1.25                  
   Expired/Forfeited     (136,334 )   $ 3.01                  
Balance at September 30, 2015     17,414,242     $ 2.21       6.09     $ 64,265,785  

Vested and Exercisable at September 30, 2015

    13,848,923     $ 1.59       5.49     $ 59,095,453  

 

XML 31 R31.htm IDEA: XBRL DOCUMENT v3.3.0.814
COMMITMENTS AND CONTINGENCIES (Tables)
9 Months Ended
Sep. 30, 2015
Commitments And Contingencies Tables  
Schedule of future minimum rental payments

As of September 30, 2015, future minimum rental payments are as follows:

 

Years Ending December 31,    
  2015 (3 months)     $ 121,698  
  2016       493,790  
  2017       507,087  
  2018       388,976  
  Minimum lease payments     $ 1,511,551  

 

XML 32 R8.htm IDEA: XBRL DOCUMENT v3.3.0.814
SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES
9 Months Ended
Sep. 30, 2015
Accounting Policies [Abstract]  
SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES

NOTE 3 – SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES

 

Impairment of Long-Lived Assets

 

We review the carrying values of property and equipment and long-lived intangible assets for impairment whenever events or changes in circumstances indicate that their carrying values may not be recoverable. There was no impairment of any long-lived assets during the three and nine months ended September 30, 2015 and 2014.

 

Fair Value of Financial Instruments

 

Our financial instruments consist primarily of accounts receivable, accounts payable and accrued expenses. The carrying amount of accounts receivable, accounts payable and accrued expenses approximates their fair value because of the short-term maturity of such instruments.

 

We categorize our assets and liabilities that are valued at fair value on a recurring basis into a three-level fair value hierarchy as defined by ASC 820, Fair Value Measurements. The fair value hierarchy gives the highest priority to quoted prices in active markets for identical assets and liabilities (Level 1) and lowest priority to unobservable inputs (Level 3). Assets and liabilities recorded in the consolidated balance sheet at fair value are categorized based on a hierarchy of inputs, as follows:

  

  Level 1 unadjusted quoted prices in active markets for identical assets or liabilities;
  Level 2 quoted prices for similar assets or liabilities in active markets or inputs that are observable for the asset or liability, either directly or indirectly through market corroboration, for substantially the full term of the financial instrument; and
  Level 3 unobservable inputs for the asset or liability.

 

At September 30, 2015 and December 31, 2014, we had no assets or liabilities that were valued at fair value on a recurring basis.

 

The fair value of indefinite-lived assets or long-lived assets is measured on a non-recurring basis using significant unobservable inputs (Level 3) in connection with any required impairment test.

 

Revenue Recognition

 

We recognize revenue on arrangements in accordance with ASC 605, Revenue Recognition. We recognize revenue only when the price is fixed or determinable, persuasive evidence of an arrangement exists, the service is performed, and collectability is reasonably assured.

 

Our OTC and prescription prenatal vitamin products are generally variations of the same product with slight modifications in formulation and marketing. The primary difference between our OTC and prescription prenatal vitamin products is the source of payment. Purchasers of our OTC prenatal vitamin products pay for the product directly while purchasers of our prescription prenatal vitamin products pay for the product via third-party payers. Both OTC and prescription prenatal vitamin products share the same marketing support team utilizing similar marketing techniques.

 

Over-the-Counter Products

 

We generate OTC revenue from product sales primarily to retail consumers. We recognize revenue from product sales upon shipment, when the rights of ownership and risk of loss have passed to the consumer. We include outbound shipping and handling fees in revenues, net, and bill them upon shipment. We include shipping expenses in cost of goods sold. A majority of our customers pay for our products with credit cards, and we usually receive the cash settlement in two to three banking days. Credit card sales minimize accounts receivable balances relative to sales. We provide an unconditional 30-day money-back return policy under which we accept product returns from our retail and eCommerce customers. We recognize our revenue from OTC sales, net of estimated returns, sales discounts, and eCommerce fees.

 

Prescription Products

 

We sell our name brand and generic prescription products primarily through drug wholesalers and retail pharmacies. We recognize revenue from prescription product sales, net of sales discounts, chargebacks, and customer rebates.

 

We accept returns of unsalable product from customers within a return period of six months prior to and up to 12 months following product expiration. Our prescription products currently have a shelf life of 24 months from the date of manufacture. As of January 1, 2015, we started estimating returns based on historical return rates and recorded actual product returns against this reserve as received. Prior to January 1, 2015, we deferred the recognition of revenue on certain arrangements until the right of return no longer existed.

 

We maintain various rebate programs in an effort to maintain a competitive position in the marketplace and to promote sales and customer loyalty. The consumer rebate program is designed to enable the end user to submit a coupon to us. If the coupon qualifies, we send a rebate check to the end user. We estimate the allowance for consumer rebates based on our experience and industry averages, which is reviewed, and adjusted if necessary, on a quarterly basis.

 

Research and Development Expenses

 

Research and development, or R&D, expenses include internal R&D activities, services of external contract research organizations, or CROs, costs of their clinical research sites, manufacturing, scale-up and validation costs, and other activities. Internal R&D activity expenses include laboratory supplies, salaries, benefits, and non-cash share-based compensation expenses. Advance payments to be expensed in future research and development activities were $948,499 at September 30, 2015, of which $755,152 was included in Other current assets and $193,347 was included in long term Prepaid expense on the accompanying consolidated balance sheets. Advance payments to be expensed in future research and development activities were $1,175,082 at December 31, 2014, of which $711,362 was included in Other current assets and $463,720 was included in long term Prepaid expense on the accompanying consolidated balance sheets. CRO activity expenses include preclinical laboratory experiments and clinical trial studies. Other activity expenses include regulatory consulting and legal fees and costs. The activities undertaken by our regulatory consultants that were classified as research and development expenses include assisting, consulting with, and advising our in-house staff with respect to various FDA submission processes, clinical trial processes, and scientific writing matters, including preparing protocols and FDA submissions. Legal activities that were classified as research and development expenses related to designing experiments to generate data for patents and to further the formulation development process for our pipeline technologies. Outside legal counsel also provided professional research and advice regarding research and development, patents and regulatory matters. These consulting and legal expenses were direct costs associated with preparing, reviewing, and undertaking work for our clinical trials and investigative drugs. We charge internal R&D activities and other activity expenses to operations as incurred. We make payments to CROs based on agreed-upon terms, which may include payments in advance of a study starting date. We expense nonrefundable advance payments for goods and services that will be used in future R&D activities when the activity has been performed or when the goods have been received rather than when the payment is made. We review and accrue CRO expenses and clinical trial study expenses based on services performed and rely on estimates of those costs applicable to the completion stage of a study as provided by CROs. As of September 30, 2015, we classified $1,213,874 of the accrued clinical study costs as long term Accrued Expenses related to the costs that will be paid at the completion of one of our clinical trials. Estimated accrued CRO costs are subject to revisions as such studies progress to completion. We charge revisions expense in the period in which the facts that give rise to the revision become known. 

 

Segment Reporting

 

We are managed and operated as one business, which is focused on creating and commercializing products targeted exclusively for women. Our business operations are managed by a single management team that reports to the President of our Company. We do not operate separate lines of business with respect to any of our products and we do not prepare discrete financial information with respect to separate products. All product sales are derived from sales in the United States. Accordingly, we view our business as one reportable operating segment.

XML 33 R32.htm IDEA: XBRL DOCUMENT v3.3.0.814
SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES (Details Narrative) - USD ($)
Sep. 30, 2015
Dec. 31, 2014
Accounting Policies [Abstract]    
Advance payments for future research and development activities $ 948,499 $ 1,175,082
Accrued Expense 1,213,874
Other assets current 755,152  
Long term prepaid expense $ 193,347 $ 463,720
XML 34 R40.htm IDEA: XBRL DOCUMENT v3.3.0.814
INTANGIBLE ASSETS (Details 1)
Sep. 30, 2015
USD ($)
Estimated amortization expense for the year:  
2015 (3 months) $ 8,692
2016 34,768
2017 34,768
2018 34,768
2019 $ 34,768
XML 35 R2.htm IDEA: XBRL DOCUMENT v3.3.0.814
CONSOLIDATED BALANCE SHEETS (Unaudited) - USD ($)
Sep. 30, 2015
Dec. 31, 2014
Current Assets:    
Cash $ 81,123,988 $ 51,361,607
Accounts receivable, net of allowance for doubtful accounts of $96,916 and $59,753, respectively 3,666,586 2,154,217
Inventory 870,059 1,182,113
Other current assets 2,120,805 1,537,407
Total current assets 87,781,438 56,235,344
Fixed assets, net 56,748 63,293
Other Assets:    
Prepaid expense 1,172,051 1,427,263
Intangible assets, net 1,324,284 1,228,588
Security deposit 125,000 125,000
Total other assets 2,621,335 2,780,851
Total assets 90,459,521 59,079,488
Current Liabilities:    
Accounts payable 5,301,625 6,327,129
Other current liabilities $ 6,386,777 3,840,639
Deferred revenue 522,613
Total current liabilities $ 11,688,402 $ 10,690,381
Long-Term Liabilities:    
Accrued Expense 1,213,874
Total liabilities $ 12,902,276 $ 10,690,381
Stockholders' Equity:    
Preferred stock - par value $0.001; 10,000,000 shares authorized; no shares issued and outstanding
Common stock - par value $0.001; 350,000,000 and 250,000,000 shares authorized; 177,787,927 and 156,097,019 issued and outstanding, respectively $ 177,788 $ 156,097
Additional paid in capital 279,723,640 182,982,846
Accumulated deficit (202,344,183) (134,749,836)
Total stockholders' equity 77,557,245 48,389,107
Total liabilities and stockholders' equity $ 90,459,521 $ 59,079,488
XML 36 R45.htm IDEA: XBRL DOCUMENT v3.3.0.814
STOCKHOLDERS' EQUITY (Details Narrative 2) - USD ($)
3 Months Ended 9 Months Ended
Sep. 30, 2015
Sep. 30, 2014
Sep. 30, 2015
Sep. 30, 2014
Dec. 31, 2014
Option exercise prices (in dollars per shares) $ 2.21   $ 2.21   $ 1.88
Share-based compensation expense $ 1,626,862 $ 1,047,493 $ 4,328,964 $ 3,341,604  
Total unrecognized estimated compensation expense $ 5,593,000   $ 5,593,000    
Recognized weighted-average period     2 years 3 months 19 days    
Options granted     1,231,000 50,000  
Stock issued for excercised warrants, shares       365,583  
Stock issued for excercised warrants, value       $ 181,000  
Warrant Exercised 1 [Member]          
Stock issued for excercised warrants, shares     945,485    
Stock issued for excercised warrants, value     $ 366,000    
Warrant Exercised 2 [Member]          
Number of shares issued 232,197   232,197    
Stock issued for excercised warrants, shares 310,000   310,000    
Minimum [Member]          
Option exercise prices (in dollars per shares) $ 0.10   $ 0.10    
Maximum [Member]          
Option exercise prices (in dollars per shares) $ 7.72   $ 7.72    
2009 Long Term Incentive Compensation Plan [Member]          
Description of plan     To provide financial incentives to employees, directors, advisers, and consultants of our company who are able to contribute towards the creation of or who have created shareholder value by providing them stock options and other stock and cash incentives, or the Awards.    
Number of shares authorized for issuance         25,000,000
Number of shares issued     15,445,768    
Options granted     1,231,000    
2012 Stock Incentive Plan [Member]          
Description of plan     Plan was designed to serve as an incentive for retaining qualified and competent key employees, officers, directors, and certain consultants and advisors of our company.    
Number of shares authorized for issuance         10,000,000
Number of shares issued     1,968,474    
XML 37 R6.htm IDEA: XBRL DOCUMENT v3.3.0.814
THE COMPANY
9 Months Ended
Sep. 30, 2015
Organization, Consolidation and Presentation of Financial Statements [Abstract]  
THE COMPANY

NOTE 1 – THE COMPANY

 

TherapeuticsMD, Inc., a Nevada corporation, or TherapeuticsMD or the Company, has three wholly owned subsidiaries, vitaMedMD, LLC, a Delaware limited liability company, or VitaMed, BocaGreenMD, Inc., a Nevada corporation, or BocaGreen, and VitaCare Prescription Services, Inc., a Florida corporation, or VitaCare. Unless the context otherwise requires, TherapeuticsMD, VitaMed, BocaGreen, and VitaCare collectively are sometimes referred to as "our company," "we," "our," or "us."

 

Nature of Business

 

We are a women’s health care product company focused on creating and commercializing products targeted exclusively for women. As of the date of these unaudited consolidated financial statements, we are focused on conducting the clinical trials necessary for regulatory approval and commercialization of our advanced hormone therapy pharmaceutical products. The drug candidates used in our clinical trials are designed to alleviate the symptoms of and reduce the health risks resulting from menopause-related hormone deficiencies, including hot flashes, osteoporosis, and vaginal discomfort. We are developing these hormone therapy drug candidates, which contain estradiol and progesterone alone or in combination, with the aim of demonstrating equivalent clinical efficacy at lower doses, thereby enabling an enhanced side effect profile compared with competing products. Our drug candidates are created from a platform of hormone technology that enables the administration of hormones with high bioavailability alone or in combination. In addition, we manufacture and distribute branded and generic prescription prenatal vitamins, as well as over-the-counter, or OTC, vitamins.

XML 38 R35.htm IDEA: XBRL DOCUMENT v3.3.0.814
FIXED ASSETS, NET (Details Narrative) - USD ($)
3 Months Ended 9 Months Ended
Sep. 30, 2015
Sep. 30, 2014
Sep. 30, 2015
Sep. 30, 2014
Property, Plant and Equipment [Abstract]        
Depreciation Expense $ 7,856 $ 7,122 $ 22,104 $ 22,713
XML 39 R22.htm IDEA: XBRL DOCUMENT v3.3.0.814
SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES (Policies)
9 Months Ended
Sep. 30, 2015
Accounting Policies [Abstract]  
Impairment of Long-Lived Assets

Impairment of Long-Lived Assets

 

We review the carrying values of property and equipment and long-lived intangible assets for impairment whenever events or changes in circumstances indicate that their carrying values may not be recoverable. There was no impairment of any long-lived assets during the three and nine months ended September 30, 2015 and 2014.

Fair Value of Financial Instruments

Fair Value of Financial Instruments

 

Our financial instruments consist primarily of accounts receivable, accounts payable and accrued expenses. The carrying amount of accounts receivable, accounts payable and accrued expenses approximates their fair value because of the short-term maturity of such instruments.

 

We categorize our assets and liabilities that are valued at fair value on a recurring basis into a three-level fair value hierarchy as defined by ASC 820, Fair Value Measurements. The fair value hierarchy gives the highest priority to quoted prices in active markets for identical assets and liabilities (Level 1) and lowest priority to unobservable inputs (Level 3). Assets and liabilities recorded in the consolidated balance sheet at fair value are categorized based on a hierarchy of inputs, as follows:

  

  Level 1 unadjusted quoted prices in active markets for identical assets or liabilities;
  Level 2 quoted prices for similar assets or liabilities in active markets or inputs that are observable for the asset or liability, either directly or indirectly through market corroboration, for substantially the full term of the financial instrument; and
  Level 3 unobservable inputs for the asset or liability.

 

At September 30, 2015 and December 31, 2014, we had no assets or liabilities that were valued at fair value on a recurring basis.

 

The fair value of indefinite-lived assets or long-lived assets is measured on a non-recurring basis using significant unobservable inputs (Level 3) in connection with any required impairment test.

 

Revenue Recognition

Revenue Recognition

 

We recognize revenue on arrangements in accordance with ASC 605, Revenue Recognition. We recognize revenue only when the price is fixed or determinable, persuasive evidence of an arrangement exists, the service is performed, and collectability is reasonably assured.

 

Our OTC and prescription prenatal vitamin products are generally variations of the same product with slight modifications in formulation and marketing. The primary difference between our OTC and prescription prenatal vitamin products is the source of payment. Purchasers of our OTC prenatal vitamin products pay for the product directly while purchasers of our prescription prenatal vitamin products pay for the product via third-party payers. Both OTC and prescription prenatal vitamin products share the same marketing support team utilizing similar marketing techniques.

 

Over-the-Counter Products

 

We generate OTC revenue from product sales primarily to retail consumers. We recognize revenue from product sales upon shipment, when the rights of ownership and risk of loss have passed to the consumer. We include outbound shipping and handling fees in revenues, net, and bill them upon shipment. We include shipping expenses in cost of goods sold. A majority of our customers pay for our products with credit cards, and we usually receive the cash settlement in two to three banking days. Credit card sales minimize accounts receivable balances relative to sales. We provide an unconditional 30-day money-back return policy under which we accept product returns from our retail and eCommerce customers. We recognize our revenue from OTC sales, net of estimated returns, sales discounts, and eCommerce fees.

 

Prescription Products

 

We sell our name brand and generic prescription products primarily through drug wholesalers and retail pharmacies. We recognize revenue from prescription product sales, net of sales discounts, chargebacks, and customer rebates.

 

We accept returns of unsalable product from customers within a return period of six months prior to and up to 12 months following product expiration. Our prescription products currently have a shelf life of 24 months from the date of manufacture. As of January 1, 2015, we started estimating returns based on historical return rates and recorded actual product returns against this reserve as received. Prior to January 1, 2015, we deferred the recognition of revenue on certain arrangements until the right of return no longer existed.

 

We maintain various rebate programs in an effort to maintain a competitive position in the marketplace and to promote sales and customer loyalty. The consumer rebate program is designed to enable the end user to submit a coupon to us. If the coupon qualifies, we send a rebate check to the end user. We estimate the allowance for consumer rebates based on our experience and industry averages, which is reviewed, and adjusted if necessary, on a quarterly basis.

Research and Development Expenses

Research and Development Expenses

 

Research and development, or R&D, expenses include internal R&D activities, services of external contract research organizations, or CROs, costs of their clinical research sites, manufacturing, scale-up and validation costs, and other activities. Internal R&D activity expenses include laboratory supplies, salaries, benefits, and non-cash share-based compensation expenses. Advance payments to be expensed in future research and development activities were $948,499 at September 30, 2015, of which $755,152 was included in Other current assets and $193,347 was included in long term Prepaid expense on the accompanying consolidated balance sheets. Advance payments to be expensed in future research and development activities were $1,175,082 at December 31, 2014, of which $711,362 was included in Other current assets and $463,720 was included in long term Prepaid expense on the accompanying consolidated balance sheets. CRO activity expenses include preclinical laboratory experiments and clinical trial studies. Other activity expenses include regulatory consulting and legal fees and costs. The activities undertaken by our regulatory consultants that were classified as research and development expenses include assisting, consulting with, and advising our in-house staff with respect to various FDA submission processes, clinical trial processes, and scientific writing matters, including preparing protocols and FDA submissions. Legal activities that were classified as research and development expenses related to designing experiments to generate data for patents and to further the formulation development process for our pipeline technologies. Outside legal counsel also provided professional research and advice regarding research and development, patents and regulatory matters. These consulting and legal expenses were direct costs associated with preparing, reviewing, and undertaking work for our clinical trials and investigative drugs. We charge internal R&D activities and other activity expenses to operations as incurred. We make payments to CROs based on agreed-upon terms, which may include payments in advance of a study starting date. We expense nonrefundable advance payments for goods and services that will be used in future R&D activities when the activity has been performed or when the goods have been received rather than when the payment is made. We review and accrue CRO expenses and clinical trial study expenses based on services performed and rely on estimates of those costs applicable to the completion stage of a study as provided by CROs. As of September 30, 2015, we classified $1,213,874 of the accrued clinical study costs as long term Accrued Expenses related to the costs that will be paid at the completion of one of our clinical trials. Estimated accrued CRO costs are subject to revisions as such studies progress to completion. We charge revisions expense in the period in which the facts that give rise to the revision become known.

Segment Reporting

Segment Reporting

 

We are managed and operated as one business, which is focused on creating and commercializing products targeted exclusively for women. Our business operations are managed by a single management team that reports to the President of our Company. We do not operate separate lines of business with respect to any of our products and we do not prepare discrete financial information with respect to separate products. All product sales are derived from sales in the United States. Accordingly, we view our business as one reportable operating segment.

XML 40 R36.htm IDEA: XBRL DOCUMENT v3.3.0.814
FIXED ASSETS, NET (Details) - USD ($)
Sep. 30, 2015
Dec. 31, 2014
Fixed assets, gross $ 201,604 $ 186,045
Accumulated depreciation (144,856) (122,752)
TOTAL FIXED ASSETS 56,748 63,293
Equipment [Member]    
Fixed assets, gross 132,150 132,150
Furniture and Fixtures [Member]    
Fixed assets, gross $ 69,454 $ 53,895
XML 41 R24.htm IDEA: XBRL DOCUMENT v3.3.0.814
OTHER CURRENT ASSETS (Tables)
9 Months Ended
Sep. 30, 2015
Deferred Costs, Capitalized, Prepaid, and Other Assets Disclosure [Abstract]  
Schedule of other current assets

Other current assets consist of the following:

  

September 30,

2015

 

December 31,

2014

Prepaid insurance  $870,949   $394,878 
Prepaid research and development costs   381,813    299,498 
Prepaid consulting   373,339    411,864 
Other receivables-related party (Note 13)   249,981    249,981 
Other prepaid costs   219,086    181,186 
Prepaid vendor deposits   25,637    —   
     TOTAL OTHER CURRENT ASSETS  $2,120,805   $1,537,407 

 

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BASIS OF PRESENTATION AND RECENTLY ISSUED ACCOUNTING PRONOUNCEMENTS
9 Months Ended
Sep. 30, 2015
Organization, Consolidation and Presentation of Financial Statements [Abstract]  
BASIS OF PRESENTATION AND RECENTLY ISSUED ACCOUNTING PRONOUNCEMENTS

NOTE 2 – BASIS OF PRESENTATION AND RECENTLY ISSUED ACCOUNTING PRONOUNCEMENTS

 

Interim Financial Statements

 

The accompanying unaudited interim consolidated financial statements of TherapeuticsMD, Inc., which include our wholly owned subsidiaries, should be read in conjunction with the audited consolidated financial statements and notes thereto included in our Annual Report on Form 10-K for the year ended December 31, 2014, as filed with the Securities and Exchange Commission, or the SEC, from which we derived the accompanying consolidated balance sheet as of December 31, 2014. The accompanying unaudited interim consolidated financial statements have been prepared in accordance with accounting principles generally accepted in the United States of America, or GAAP, for interim financial information and with the instructions to Form 10-Q and Article 10 of Regulation S-X. Accordingly, since they are interim statements, the accompanying unaudited interim consolidated financial statements do not include all of the information and notes required by GAAP for complete financial statements. The accompanying unaudited interim consolidated financial statements reflect all adjustments, consisting of normal recurring adjustments, that are, in the opinion of our management, necessary to a fair statement of the results for the interim periods presented. Interim results are not necessarily indicative of results for a full year, or any other interim period.

 

Recently Issued Accounting Pronouncements

 

In July 2015, the Financial Accounting Standards Board, or FASB, issued final guidance that requires entities to measure inventory at the lower of cost or net realizable value rather than at the lower of cost or market (LOCOM). The guidance applies only to inventories for which cost is determined by methods other than last-in first-out (LIFO) or the retail inventory method (RIM). Entities that use LIFO or RIM will continue to use existing impairment models. The new guidance does not change the calculation of net realizable value that entities are required to calculate when applying existing LOCOM guidance. Net realizable value is the estimated selling price in the ordinary course of business, less reasonably predictable costs of completion, disposal and transportation. Under the new guidance, however, entities will no longer need to calculate other measures of “market.” The guidance is effective for public business entities for fiscal years beginning after December 15, 2016, and interim periods within those fiscal years. Early adoption is permitted. We are currently evaluating the impact of this guidance on our consolidated financial statements and disclosures.

 

In June 2015, the FASB issued Accounting Standards Update, or ASU, No. 2015-10, Technical Corrections and Improvements, to correct differences between original guidance and the Accounting Standards Codification, or ASC, clarify the guidance, correct references and make minor improvements affecting a variety of topics. Amendments that the FASB deemed more substantive are effective for fiscal years, and interim periods within those fiscal years, beginning after December 15, 2015. The other amendments are effective immediately. We do not expect the adoption of ASU 2015-10 to have a material effect on our consolidated financial statements and disclosures.

 

In August 2014, the FASB issued ASU No. 2014-15, Presentation of Financial Statements-Going Concern (Subtopic 205-40): Disclosure of Uncertainties about an Entity’s Ability to Continue as a Going Concern. ASU 2014-15 requires management to evaluate whether there are conditions and events that raise substantial doubt about the entity’s ability to continue as a going concern within one year after the financial statements are issued (or available to be issued when applicable) and, if so, disclose that fact. ASU 2014-15 is effective for annual periods ending after December 15, 2016 and interim periods within annual periods beginning after December 15, 2016. Early adoption is permitted for annual or interim reporting periods for which the financial statements have not previously been issued. We do not expect the adoption of ASU 2014-15 to have a material effect on our consolidated financial statements and disclosures.

 

In May 2014, the FASB and the International Accounting Standards Board (IASB) issued ASU No. 2014-09, Revenue from Contracts with Customers (Topic 606). The standard’s core principle is that a company will recognize revenue when it transfers promised goods or services to customers in an amount that reflects the consideration to which the company expects to be entitled in exchange for those goods or services. In doing so, companies will need to use more judgment and make more estimates than under previous guidance. These may include identifying performance obligations in the contract, estimating the amount of variable consideration to include in the transaction price and allocating the transaction price to each separate performance obligations. In July 2015, the FASB approved the proposal to defer the effective date of ASU 2014-09 standard by one year. Early adoption is permitted after December 15, 2016, and the standard is effective for public entities for annual reporting periods beginning after December 15, 2017 and interim periods therein. We are currently evaluating the impact of ASU 2014-09 on our consolidated financial statements and disclosures.

 

We do not believe there would have been a material effect on the accompanying consolidated financial statements had any other recently issued, but not yet effective, accounting standards been adopted in the current period.

XML 44 R3.htm IDEA: XBRL DOCUMENT v3.3.0.814
CONSOLIDATED BALANCE SHEETS (Unaudited) (Parenthetical) - USD ($)
Sep. 30, 2015
Dec. 31, 2014
Statement of Financial Position [Abstract]    
Allowance for doubtful accounts $ 96,916 $ 59,753
Preferred stock, par value (in dollars per share) $ 0.001 $ 0.001
Preferred stock, shares authorized 10,000,000 10,000,000
Preferred stock, shares issued 0 0
Preferred stock, shares outstanding 0 0
Common stock, par value (in dollars per share) $ 0.001 $ 0.001
Common stock, shares authorized 350,000,000 250,000,000
Common stock, shares issued 177,787,927 156,097,019
Common stock, shares outstanding 177,787,927 156,097,019
XML 45 R17.htm IDEA: XBRL DOCUMENT v3.3.0.814
INCOME TAXES
9 Months Ended
Sep. 30, 2015
Income Tax Disclosure [Abstract]  
INCOME TAXES

NOTE 12 – INCOME TAXES

 

Deferred income tax assets and liabilities are determined based upon differences between the financial reporting and tax basis of assets and liabilities and are measured using the enacted tax rates and laws that will be in effect when the differences are expected to reverse. We do not expect to pay any significant federal or state income tax for 2015 as a result of (i) the losses recorded during the nine months ended September 30, 2015, (ii) additional losses expected for the remainder of 2015, and/or (iii) net operating loss carry forwards from prior years. Accounting standards require the consideration of a valuation allowance for deferred tax assets if it is "more likely than not" that some component or all of the benefits of deferred tax assets will not be realized. As of September 30, 2015, we maintain a full valuation allowance for all deferred tax assets. Based on these requirements, no provision or benefit for income taxes has been recorded. There were no recorded unrecognized tax benefits at the end of the reporting period.

XML 46 R1.htm IDEA: XBRL DOCUMENT v3.3.0.814
Document and Entity Information - shares
9 Months Ended
Sep. 30, 2015
Nov. 02, 2015
Document And Entity Information    
Entity Registrant Name TherapeuticsMD, Inc.  
Entity Central Index Key 0000025743  
Document Type 10-Q  
Document Period End Date Sep. 30, 2015  
Amendment Flag false  
Current Fiscal Year End Date --12-31  
Entity a Well-known Seasoned Issuer No  
Entity a Voluntary Filer No  
Entity's Reporting Status Current Yes  
Entity Filer Category Accelerated Filer  
Entity Common Stock, Shares Outstanding   177,848,041
Document Fiscal Period Focus Q3  
Document Fiscal Year Focus 2015  
XML 47 R18.htm IDEA: XBRL DOCUMENT v3.3.0.814
RELATED PARTIES
9 Months Ended
Sep. 30, 2015
Related Party Transactions [Abstract]  
RELATED PARTIES

NOTE 13 – RELATED PARTIES

 

On February 29, 2012, Cooper C. Collins, who was then president and largest shareholder of Pernix Therapeutics, LLC, or Pernix, was elected to serve on our board of directors. From time to time, we have entered into agreements with Pernix in the normal course of business. All such agreements are reviewed by independent directors of our company or a committee consisting of independent directors of our company.

 

During the nine months ended September 30, 2015 and 2014, we did not engage in any transactions with Pernix. At September 30, 2015 and December 31, 2014, there were amounts due Pernix of approximately $46,000.

 

Additionally, there were amounts due to us from Pernix for legal fee reimbursement relating to a litigation matter stemming from a license and supply agreement in the amounts of approximately $250,000 at both September 30, 2015 and December 31, 2014.

XML 48 R4.htm IDEA: XBRL DOCUMENT v3.3.0.814
CONSOLIDATED STATEMENTS OF OPERATIONS (Unaudited) - USD ($)
3 Months Ended 9 Months Ended
Sep. 30, 2015
Sep. 30, 2014
Sep. 30, 2015
Sep. 30, 2014
Income Statement [Abstract]        
Revenues, net $ 5,190,175 $ 4,186,261 $ 14,513,158 $ 10,768,572
Cost of goods sold 1,193,965 1,068,605 3,270,695 2,792,268
Gross profit 3,996,210 3,117,656 11,242,463 7,976,304
Operating expenses:        
Sales, general, and administrative 7,060,944 6,043,354 20,089,998 16,610,015
Research and development 16,421,753 14,909,430 58,789,302 29,052,149
Depreciation and amortization 16,548 12,747 44,400 39,909
Total operating expense 23,499,245 20,965,531 78,923,700 45,702,073
Operating loss (19,503,035) (17,847,875) (67,681,237) (37,725,769)
Other income (expense):        
Miscellaneous income 27,630 6,260 71,728 43,411
Interest income 2,760 9,364 15,162 27,756
Financing costs       (260,027)
Total other income (expense) 30,390 15,624 86,890 (188,860)
Loss before income taxes (19,472,645) (17,832,251) (67,594,347) (37,914,629)
Net loss $ (19,472,645) $ (17,832,251) $ (67,594,347) $ (37,914,629)
Loss per share, basic and diluted:        
Net loss per share, basic and diluted $ (0.11) $ (0.12) $ (0.39) $ (0.26)
Weighted average number of common shares outstanding, basic and diluted 177,206,168 152,200,455 171,589,595 147,594,810
XML 49 R12.htm IDEA: XBRL DOCUMENT v3.3.0.814
PREPAID EXPENSE
9 Months Ended
Sep. 30, 2015
Prepaid Expense and Other Assets [Abstract]  
PREPAID EXPENSE

NOTE 7 – PREPAID EXPENSE

 

Prepaid expense (long-term) consists of the following:

  

September 30,

2015

 

December 31,

2014

Prepaid manufacturing costs  $978,704   $963,543 
Prepaid research and development costs   193,347    463,720 
     TOTAL PREPAID EXPENSE  $1,172,051   $1,427,263 
XML 50 R11.htm IDEA: XBRL DOCUMENT v3.3.0.814
FIXED ASSETS, NET
9 Months Ended
Sep. 30, 2015
Property, Plant and Equipment [Abstract]  
FIXED ASSETS

NOTE 6 – FIXED ASSETS, NET

 

Fixed assets, net consist of the following:

  

September 30,

2015

 

December 31,

2014

Equipment  $132,150   $132,150 
Furniture and fixtures   69,454    53,895 
    201,604    186,045 
Accumulated depreciation   (144,856)   (122,752)
     TOTAL FIXED ASSETS, NET  $56,748   $63,293 

 

Depreciation expense for the three months ended September 30, 2015 and 2014 was $7,856 and $7,122, respectively, and $22,104 and $22,713 for the nine months ended September 30, 2015 and 2014, respectively.

XML 51 R23.htm IDEA: XBRL DOCUMENT v3.3.0.814
INVENTORY (Tables)
9 Months Ended
Sep. 30, 2015
Inventory Disclosure [Abstract]  
Schedule of Inventory

Inventory consists of the following:

 

  

September 30,

2015

 

December 31,

2014

Finished product  $787,232   $874,294 
Raw material   82,827    155,341 
Deferred costs   —      152,478 
     TOTAL INVENTORY  $870,059   $1,182,113 
XML 52 R19.htm IDEA: XBRL DOCUMENT v3.3.0.814
BUSINESS CONCENTRATIONS
9 Months Ended
Sep. 30, 2015
Risks and Uncertainties [Abstract]  
BUSINESS CONCENTRATIONS

NOTE 14 - BUSINESS CONCENTRATIONS

 

We purchase our products from several suppliers with approximately 54% and 77% of our purchases supplied from one vendor for the nine months ended September 30, 2015 and 2014, respectively.

 

We sell our prescription prenatal vitamin products to wholesale distributors, specialty pharmacies, specialty distributors, and chain drug stores that generally sell products to retail pharmacies, hospitals, and other institutional customers. Revenue generated from four major customers accounted for approximately 90% and 95% of our recognized revenue for the nine months ended September 30, 2015 and 2014, respectively.

 

Customers that generated more than 10% of our sales are designated as customers “A”, “B”, “C” and “D”.

During the nine months ended September 30, 2015, two customers generated more than 10% of revenues and during the nine months ended September 30, 2014, four customers generated more than 10% of revenues. During the nine months ended September 30, 2015, customer A generated approximately $6,930,000 in revenues and customer B generated approximately $3,005,000 in revenues. During the nine months ended September 30, 2014, customers A, B, C and D generated approximately $3,930,000, $1,846,000, $1,590,000 and $1,555,000 in sales, respectively.

XML 53 R15.htm IDEA: XBRL DOCUMENT v3.3.0.814
NET LOSS PER SHARE
9 Months Ended
Sep. 30, 2015
Net Loss Per Share  
NET LOSS PER SHARE

NOTE 10 – NET LOSS PER SHARE

 

We calculate basic and diluted net loss per share allocable to common stockholders using the weighted-average number of shares of common stock, par value $0.001 per share, or Common Stock outstanding during the period, less any shares subject to repurchase or forfeiture. There were no shares of our Common Stock outstanding subject to repurchase or forfeiture for the three and nine months ended September 30, 2015 and 2014.

 

Since we are in a net loss position, we have excluded outstanding stock options, all of which are subject to forfeiture, as well as warrants for the purchase of our Common Stock from our calculation of diluted net loss per share.

 

The table below presents the potentially dilutive securities that would have been included in our calculation of diluted net loss per share allocable to common stockholders if they were not antidilutive for the periods presented.

 

   As of September 30,
   2015  2014
Stock options   17,414,242    16,851,943 
Warrants   12,722,431    13,927,916 
    30,136,673    30,779,859 
XML 54 R13.htm IDEA: XBRL DOCUMENT v3.3.0.814
INTANGIBLE ASSETS
9 Months Ended
Sep. 30, 2015
Goodwill and Intangible Assets Disclosure [Abstract]  
INTANGIBLE ASSETS

NOTE 8 – INTANGIBLE ASSETS, NET

 

The following table sets forth the gross carrying amount, accumulated amortization and net carrying amount of our intangible assets as of September 30, 2015 and December 31, 2014:

 

    September 30, 2015
   

 

Gross Carrying Amount

 

 

Accumulated Amortization

 

 Net

Amount

  Weighted- Average Amortization Period (yrs.)
Amortizing intangible assets:                                
   OPERA® software patent   $ 31,951     $ (3,994 )   $ 27,957       14  
   Development costs of                                
      corporate website     91,743       (91,743 )     —         n/a  
   Approved hormone                                
      therapy drug                                
      candidate patents     605,502       (40,199 )     565,303       17.25  
Non-amortizing intangible                                
  assets:                                
   Hormone therapy drug                                
      candidate patents                                
      (pending)     585,241       —         585,241       n/a  
   Multiple trademarks for                                
      vitamins/supplements     145,783       —         145,783       indefinite  
      Total   $ 1,460,220     $ (135,936 )   $ 1,324,284          

  

   

 December 31, 2014

   

 

Gross Carrying Amount

 

 

Accumulated Amortization

 

 Net

Amount

  Weighted- Average Amortization Period (yrs.)
Amortizing intangible assets:                                
   OPERA® software patent   $ 31,951     $ (2,496 )   $ 29,455       14.75  
   Development costs of                                
      corporate website     91,743       (91,743 )     —         n/a  
   Approved hormone                                
      therapy drug                                
      candidate patents     439,184       (19,401 )     419,783       18  
Non-amortizing intangible                                
  assets:                                
   Hormone therapy drug                                
      candidate patents                                
      (pending)     675,982       —         675,982       n/a  
   Multiple trademarks for                                
      vitamins/supplements     103,368       —         103,368       indefinite  
      Total   $ 1,342,228     $ (113,640 )   $ 1,228,588          

 

We capitalize external costs, consisting primarily of legal costs, related to securing our patents and trademarks. Once a patent is granted, we amortize the capitalized patent costs over the remaining life of the patent using the straight-line method. If the patent is not granted, we write-off any capitalized patent costs at that time.

 

Trademarks are perpetual and are not amortized. As of September 30, 2015, the remaining life related to OPERA® patent was approximately 14 years and the remaining life related to the approved hormone therapy drug candidate patents was approximately 17 years. During the three and nine months ended September 30, 2015 and 2014, there was no impairment recognized.

 

In addition to numerous pending patent applications, as of September 30, 2015, we had 13 issued patents, including:

· one method patent that relates to our OPERA® information technology platform, which is owned by us and is a U.S. jurisdiction patent with an expiration date in 2029;
  · twelve utility patents that relate to our combination progesterone and estradiol formulations, which are owned by us and are U.S. jurisdiction patents with expiration dates in 2032. We have pending patent applications with respect to certain of these patents in Argentina, Australia, Canada, the European Union, Israel, Mexico, Brazil, Japan, Russia, South Africa and South Korea.

 

Amortization expense was $8,692 and $5,625 for the three months ended September 30, 2015 and 2014, respectively and $22,296 and $17,196 for the nine months ended September 30, 2015 and 2014, respectively. Estimated amortization expense for the next five years is as follows:

 

Year Ending December 31,   Estimated Amortization
  2015 (3 months)     $ 8,692  
  2016     $ 34,768  
  2017     $ 34,768  
  2018     $ 34,768  
  2019     $ 34,768  

 

XML 55 R14.htm IDEA: XBRL DOCUMENT v3.3.0.814
OTHER CURRENT LIABILITIES
9 Months Ended
Sep. 30, 2015
Other Liabilities Disclosure [Abstract]  
OTHER CURRENT LIABILITIES

NOTE 9 – OTHER CURRENT LIABILITIES

 

Other current liabilities consist of the following:

  

September 30,

2015

 

December 31,

2014

Accrued clinical trial costs  $3,528,061   $1,706,542 
Accrued payroll, bonuses and commission costs   930,913    814,205 
Accrued legal and accounting expense   615,946    276,470 
Accrued compensated absences   490,170    442,430 
Other accrued expenses   388,268    185,965 
Allowance for coupons and returns   208,361    90,446 
Allowance for wholesale distributor fees   96,440    160,503 
Accrued rent   86,998    91,368 
Accrued royalties   41,620    72,710 
     TOTAL OTHER CURRENT LIABILITIES  $6,386,777   $3,840,639 
XML 56 R16.htm IDEA: XBRL DOCUMENT v3.3.0.814
STOCKHOLDERS' EQUITY
9 Months Ended
Sep. 30, 2015
Stockholders' Equity:  
STOCKHOLDERS' EQUITY

NOTE 11 – STOCKHOLDERS’ EQUITY

 

Preferred Stock

 

At September 30, 2015, we had 10,000,000 shares of Preferred Stock, par value $0.001, authorized for issuance, of which no shares of Preferred Stock were issued or outstanding.

 

Common Stock

 

At September 30, 2015, we had 350,000,000 shares of Common Stock authorized, of which 177,787,927 shares of Common Stock were issued and outstanding.

 

On July 9, 2015, we entered into an underwriting agreement with Stifel, Nicolaus & Company, Incorporated and Guggenheim Securities, LLC, as the representatives of the several underwriters, or the Stifel Underwriters, relating to an underwritten public offering of 3,846,154 shares of Common Stock at a public offering price of $7.80 per share. Under the terms of the underwriting agreement, we granted the Stifel Underwriters a 30-day option to purchase up to an aggregate of 576,923 additional shares of Common Stock, which option was exercised in full. The net proceeds to us from the offering were approximately $32.2 million, after deducting underwriting discounts and commissions and other estimated offering expenses payable by us. The offering closed on July 15, 2015 and we issued 4,423,077 shares of our Common Stock.

 

On February 10, 2015, we entered into an underwriting agreement, or the Cowen Agreement, with Cowen and Company, LLC, as the representative of the several underwriters, or the Cowen Underwriters, relating to an underwritten public offering of 13,580,246 shares of Common Stock, at a public offering price of $4.05 per share. Under the terms of the Cowen Agreement, we granted the Cowen Underwriters a 30-day option to purchase up to an aggregate of 2,037,036 additional shares of Common Stock, which option was exercised in full. The net proceeds from the offering were approximately $59.1 million, after deducting underwriting discounts and commissions and other estimated offering expenses payable by us. The offering closed on February 17, 2015 and we issued 15,617,282 shares of our Common Stock.

 

On July 29, 2014, we entered into an underwriting agreement with Goldman Sachs & Co, or Goldman Sachs, as the representative of the underwriters named therein, or the Goldman Sachs Underwriters, relating to an underwritten public offering of 8,565,310 shares of Common Stock. The price to the public in the offering was $4.67 per share. Under the terms of the underwriting agreement, we granted the Goldman Sachs Underwriters a 30-day option to purchase up to an additional 1,284,796 shares of Common Stock. On July 30, 2014, the Goldman Sachs Underwriters exercised their option to purchase the additional 1,284,796 shares of Common Stock. Net proceeds from this offering were approximately $42.8 million, after deducting underwriting discounts and commissions and other offering expenses. The offering closed on August 4, 2014 and we issued 9,850,106 shares of our Common Stock.

 

Exercises During 2015

 

During the three months ended September 30, 2015, certain individuals exercised stock options to purchase 95,000 shares of Common Stock for $98,478 in cash. During the nine months ended September 30, 2015, certain individuals exercised stock options to purchase 472,867 shares of Common Stock for $589,829 in cash.

 

Exercises During 2014

 

During the nine months ended September 30, 2014, certain individuals exercised stock options to purchase 793,800 shares of Common Stock. Stock options to purchase shares of Common Stock were exercised as follows: (i) 674,193 options for $315,546 in cash and (ii) 119,607 options, pursuant to the stock options’ cashless provision, wherein 113,837 shares of Common Stock were issued. Also during the nine months ended September 30, 2014, we issued 50,000 shares of Common Stock to an employee upon the vesting of restricted stock units that were granted in December 2013.

 

Warrants to Purchase Common Stock

 

As of September 30, 2015, we had warrants outstanding to purchase an aggregate of 12,772,431 shares of Common Stock with a weighted-average contractual remaining life of 1.92 years, and exercise prices ranging from $0.24 to $6.35 per share, resulting in a weighted average exercise price of $1.93 per share.

  

The valuation methodology used to determine the fair value of our warrants is the Black-Scholes-Merton valuation model, or the Black-Scholes Model. The Black-Scholes Model requires the use of a number of assumptions, including volatility of the stock price, the risk-free interest rate and the term of the warrant.

 

In January 2013, we granted warrants to purchase 1,250,000 shares of Common Stock in connection with the issuance of a Revolving Credit Note to Plato and Associates, LLC, or the Plato Warrant. The Plato Warrant has an exercise price of $3.20 per share. The Plato Warrant vested on October 31, 2013 and may be exercised prior to its expiration on January 31, 2019. The Plato Warrant, with a fair value of $1,711,956, was valued on the date of the grant using a term of six years; a volatility of 44.29%; risk free rate of 0.88%; and a dividend yield of 0%. For the nine months ended September 30, 2015 and 2014, $0 and $260,027, respectively, was recorded as financing costs in connection with the issuance of the Plato Warrant on the accompanying consolidated financial statements.

 

In May 2013, we entered into a consulting agreement with Sancilio & Company, Inc., or SCI, to develop drug technology to be used in our hormone replacement drug candidates. These services include support of our efforts to successfully obtain U.S. Food and Drug Administration, or the FDA, approval for our drug candidates, including a vaginal capsule for the treatment of vulvar and vaginal atrophy, or VVA. In connection with the agreement, SCI agreed to forfeit its rights to receive warrants to purchase 833,000 shares of Common Stock that were to be granted pursuant to the terms of a prior consulting agreement dated May 17, 2012. As consideration under the agreement, we agreed to grant to SCI a warrant to purchase 850,000 shares of Common Stock at $2.01 per share that has vested or will vest, as applicable, as follows:

 

  1. 283,333 shares were earned on May 11, 2013 upon acceptance of an Investigational New Drug application by the FDA for an estradiol-based drug candidate in a softgel vaginal capsule for the treatment of VVA; however, pursuant to the terms of the consulting agreement, the shares did not vest until June 30, 2013.  The fair value of $405,066 for the shares vested on June 30, 2013 was determined by using the Black-Scholes Model on the date of vesting using a term of five years; a volatility of 45.89%; risk free rate of 1.12%; and a dividend yield of 0%.  We recorded the entire $405,066 as non-cash compensation as of June 30, 2013;

 

  2. 283,333 shares vested on June 30, 2013.  The fair value of $462,196 for these shares was determined by using the Black-Scholes Model on the date of the vesting using a term of five years; a volatility of 45.84%; risk free rate of 1.41%; and a dividend yield of 0%.  As of September 30, 2015, we recorded $115,543 in other current assets in the accompanying consolidated financial statements with respect to such shares.  During the three and nine month periods ended September 30, 2015 and 2014, we recorded $38,517 and $115,551, respectively, as non-cash compensation in the accompanying consolidated financial statements with respect to such shares; and

 

  3. 283,334 shares will vest upon the receipt by us of any final FDA approval of a drug candidate that SCI helped us design.  It is anticipated that this event will not occur before December 2016.

 

As of September 30, 2015, unamortized costs associated with the SCI warrants issued in 2013 and 2012 totaled approximately $567,000 and will be recognized over a period of 1.75 years.

 

During the nine months ended September 30, 2015, we granted warrants to purchase 50,000 shares of Common Stock to an outside consultant at an exercise price of $6.35 and the expiration date of April 6, 2020. The total non-cash compensation expense related to this warrant was $42,266 and $86,008, respectively, for the three and nine months ended September 30, 2015.

 

Warrant exercises

 

During the three months ended September 30, 2015, certain individuals and an entity exercised warrants to purchase 310,000 shares of Common Stock pursuant to the warrants’ cashless exercise provisions, wherein 232,197 shares of Common Stock were issued. During the nine months ended September 30, 2015, certain individuals and an entity exercised warrants to purchase 1,255,485 shares of Common Stock as follows: (i) 945,485 shares of Common Stock were issued for $366,000 in cash and (ii) warrants to purchase 310,000 shares of Common Stock were exercised pursuant to the warrants’ cashless exercise provisions, wherein 232,197 shares of Common Stock were issued.

 

During the nine months ended September 30, 2014, certain individuals exercised warrants to purchase 365,583 shares of Common Stock for $181,000 in cash.

 

Options to Purchase Common Stock

 

In 2009, we adopted the 2009 Long Term Incentive Compensation Plan, or the 2009 Plan, to provide financial incentives to employees, directors, advisers, and consultants of our company who are able to contribute towards the creation of or who have created stockholder value by providing them stock options and other stock and cash incentives, or the Awards. The Awards available under the 2009 Plan consist of stock options, stock appreciation rights, restricted stock, restricted stock units, performance stock, performance units, and other stock or cash awards as described in the 2009 Plan. There are 25,000,000 shares authorized for issuance thereunder. During the nine months ended September 30, 2015, we granted 1,231,000 non-qualified stock options under the 2009 Plan. As of September 30, 2015, there were non-qualified stock options to purchase 15,445,768 shares of Common Stock outstanding under the 2009 Plan.

 

In 2012, we adopted the 2012 Stock Incentive Plan, or the 2012 Plan, a non-qualified plan that was amended in August 2013. The 2012 Plan was designed to serve as an incentive for retaining qualified and competent key employees, officers, directors, and certain consultants and advisors of our company. There are 10,000,000 shares of Common Stock authorized for issuance thereunder. As of September 30, 2015, there were non-qualified stock options to purchase 1,968,474 shares of Common Stock outstanding under the 2012 Plan.

 

The valuation methodology used to determine the fair value of stock options is the Black-Scholes Model. The Black-Scholes Model requires the use of a number of assumptions including estimated volatility of the stock price, the risk-free interest rate, and the expected life of the stock options. The assumptions used in the Black-Scholes Model during the nine months ended September 30, 2015 and 2014 are set forth in the table below.

 

    Nine Months Ended September 30,
    2015   2014
Risk-free interest rate     1.47-1.54 %     1.68-1.77 %
Volatility     58.77-62.94 %     69.15-70.93 %
Term (in years)     5.27-6.25       5-6.25  
Dividend yield     0.00 %     0.00 %

 

The risk-free interest rate assumption is based upon observed interest rates on zero coupon U.S. Treasury bonds whose maturity period is appropriate for the expected term. Estimated volatility is a measure of the amount by which the price of our Common Stock is expected to fluctuate each year during the term of an award. Our estimated volatility is an average of the historical volatility of the stock prices of our peer entities whose stock prices were publicly available. Our calculation of estimated volatility is based on historical stock prices over a period equal to the term of the awards. We used the historical volatility of our peer entities due to the lack of sufficient historical data on our stock price. The average expected life is based on the contractual terms of the stock option using the simplified method.

  

A summary of activity under the 2009 and 2012 Plans and related information follows:

 

    Number of Shares Underlying Stock Options  

 

Weighted Average Exercise Price

 

Weighted Average

Remaining

Contractual

Life in Years

 

 

 

Aggregate Intrinsic Value

Balance at December 31, 2014     16,792,443     $ 1.88       6.92     $ 43,996,311  
   Granted     1,231,000     $ 6.38                  
   Exercised     (472,867 )   $ 1.25                  
   Expired/Forfeited     (136,334 )   $ 3.01                  
Balance at September 30, 2015     17,414,242     $ 2.21       6.09     $ 64,265,785  

Vested and Exercisable at September 30, 2015

    13,848,923     $ 1.59       5.49     $ 59,095,453  

 

 

At September 30, 2015, our outstanding stock options had exercise prices ranging from $0.10 to $7.72 per share.

 

Share-based compensation expense for options recognized in our results of operations (based on vested awards) for the three and nine months ended September 30, 2015 were $1,626,862 and $4,328,964, respectively, and $1,047,493 and $3,341,604, respectively, for the same periods in 2014. ASC 718-10 requires forfeitures to be estimated at the time of grant and revised in subsequent periods if actual forfeitures differ from the estimates. At September 30, 2015, total unrecognized estimated compensation expense related to unvested options granted prior to that date was approximately $5,593,000 which may be adjusted for future changes in forfeitures. This cost is expected to be recognized over a weighted-average period of 2.3 years. No tax benefit was realized due to a continued pattern of operating losses.

 

XML 57 R34.htm IDEA: XBRL DOCUMENT v3.3.0.814
OTHER CURRENT ASSETS (Details) - USD ($)
Sep. 30, 2015
Dec. 31, 2014
Other Current Assets    
Prepaid insurance $ 870,949 $ 394,878
Prepaid research and development costs 381,813 299,498
Prepaid consulting 373,339 411,864
Other receivables-related party (Note 13) 249,981 249,981
Other prepaid costs 219,086 181,186
Prepaid vendor deposits 25,637  
TOTAL OTHER CURRENT ASSETS $ 2,120,805 $ 1,537,407
XML 58 R51.htm IDEA: XBRL DOCUMENT v3.3.0.814
COMMITMENTS AND CONTINGENCIES (Details)
Sep. 30, 2015
USD ($)
Future minimum rental payments, year ending December 31,  
2015 (3 months) $ 121,698
2016 493,790
2017 507,087
2018 388,976
Minimum lease payments $ 1,511,551
XML 59 R21.htm IDEA: XBRL DOCUMENT v3.3.0.814
SUBSEQUENT EVENTS
9 Months Ended
Sep. 30, 2015
Subsequent Events [Abstract]  
SUBSEQUENT EVENTS

NOTE 16 – SUBSEQUENT EVENTS

 

In October 2015, we completed enrollment in the REPLENISH trial, a phase 3 study of TX-001HR in postmenopausal women with an intact uterus. The trial was designed to enroll approximately 1,750 patients at approximately 100 sites.

XML 60 R26.htm IDEA: XBRL DOCUMENT v3.3.0.814
PREPAID EXPENSE (Tables)
9 Months Ended
Sep. 30, 2015
Prepaid Expense and Other Assets [Abstract]  
Schedule of prepaid expense

Prepaid expense (long-term) consists of the following:

  

September 30,

2015

 

December 31,

2014

Prepaid manufacturing costs  $978,704   $963,543 
Prepaid research and development costs   193,347    463,720 
     TOTAL PREPAID EXPENSE  $1,172,051   $1,427,263 
XML 61 R49.htm IDEA: XBRL DOCUMENT v3.3.0.814
BUSINESS CONCENTRATIONS (Details Narrative) - USD ($)
3 Months Ended 9 Months Ended
Sep. 30, 2015
Sep. 30, 2014
Sep. 30, 2015
Sep. 30, 2014
Concentration Risk [Line Items]        
Revenues $ 5,190,175 $ 4,186,261 $ 14,513,158 $ 10,768,572
Supplier Concentration Risk [Member]        
Concentration Risk [Line Items]        
Concentration Risk     54.00% 77.00%
Customer Concentration Risk [Member] | Sales Revenue [Member]        
Concentration Risk [Line Items]        
Concentration Risk     90.00% 95.00%
Customer Concentration Risk [Member] | Sales Revenue [Member] | Minimum [Member]        
Concentration Risk [Line Items]        
Concentration Risk     10.00% 10.00%
Customer A [Member] | Sales Revenue [Member]        
Concentration Risk [Line Items]        
Revenues     $ 6,930,000 $ 3,930,000
Customer B [Member] | Sales Revenue [Member]        
Concentration Risk [Line Items]        
Revenues     $ 3,005,000 1,846,000
Customer C [Member] | Sales Revenue [Member]        
Concentration Risk [Line Items]        
Revenues       1,590,000
Customer D [Member] | Sales Revenue [Member]        
Concentration Risk [Line Items]        
Revenues       $ 1,555,000
XML 62 R41.htm IDEA: XBRL DOCUMENT v3.3.0.814
OTHER CURRENT LIABILITIES (Details) - USD ($)
Sep. 30, 2015
Dec. 31, 2014
Other Liabilities Disclosure [Abstract]    
Accrued clinical trial costs $ 3,528,061 $ 1,706,542
Accrued payroll, bonuses and commission costs 930,913 814,205
Accrued legal and accounting expense 615,946 276,470
Accrued compensated absences 490,170 442,430
Other accrued expenses [1] 388,268 185,965
Allowance for coupons and returns 208,361 90,446
Allowance for wholesale distributor fees 96,440 160,503
Accrued rent 86,998 91,368
Accrued royalties 41,620 72,710
TOTAL OTHER CURRENT LIABILITIES $ 6,386,777 $ 3,840,639
[1] In June 2008, we declared and paid a special dividend of $0.40 per share of our Common Stock to all stockholders of record as of June 10, 2008, of which $41,359 remained unclaimed by certain shareholders at March 31, 2015 and December 31, 2014.
XML 63 R5.htm IDEA: XBRL DOCUMENT v3.3.0.814
CONSOLIDATED STATEMENTS OF CASH FLOWS (Unaudited) - USD ($)
9 Months Ended
Sep. 30, 2015
Sep. 30, 2014
CASH FLOWS FROM OPERATING ACTIVITIES    
Net loss $ (67,594,347) $ (37,914,629)
Adjustments to reconcile net loss to net cash flows used in operating activities:    
Depreciation 22,104 22,713
Amortization of intangible assets 22,296 17,196
Provision for doubtful accounts 37,163 2,594
Stock based compensation 4,740,906 3,934,836
Amortization of deferred financing costs   260,027
Changes in operating assets and liabilities:    
Accounts receivable (1,549,532) (460,565)
Inventory 312,054 31,673
Other current assets (621,923) 197,569
Other assets (15,162) (17,069)
Accounts payable (1,025,504) 3,534,462
Deferred revenue (522,613) (754,431)
Other current liabilities 2,546,138 909,890
Long term accrued expenses 1,213,874  
Net cash flows used in operating activities (62,434,546) (30,235,734)
CASH FLOWS FROM INVESTING ACTIVITIES    
Patent costs (117,992) (193,349)
Purchase of property and equipment (15,559) (30,962)
Net cash flows used in investing activities (133,551) (224,311)
CASH FLOWS FROM FINANCING ACTIVITIES    
Proceeds from sale of common stock, net of costs 91,374,649 42,771,353
Proceeds from exercise of options 589,829 315,546
Proceeds from exercise of warrants 366,000 181,000
Net cash flows provided by financing activities 92,330,478 43,267,899
Increase in cash 29,762,381 12,807,854
Cash, beginning of period 51,361,607 54,191,260
Cash, end of period $ 81,123,988 $ 66,999,114
XML 64 R10.htm IDEA: XBRL DOCUMENT v3.3.0.814
OTHER CURRENT ASSETS
9 Months Ended
Sep. 30, 2015
Deferred Costs, Capitalized, Prepaid, and Other Assets Disclosure [Abstract]  
OTHER CURRENT ASSETS

NOTE 5 – OTHER CURRENT ASSETS

 

Other current assets consist of the following:

  

September 30,

2015

 

December 31,

2014

Prepaid insurance  $870,949   $394,878 
Prepaid research and development costs   381,813    299,498 
Prepaid consulting   373,339    411,864 
Other receivables-related party (Note 13)   249,981    249,981 
Other prepaid costs   219,086    181,186 
Prepaid vendor deposits   25,637    —   
     TOTAL OTHER CURRENT ASSETS  $2,120,805   $1,537,407 
XML 65 R27.htm IDEA: XBRL DOCUMENT v3.3.0.814
INTANGIBLE ASSETS (Tables)
9 Months Ended
Sep. 30, 2015
Goodwill and Intangible Assets Disclosure [Abstract]  
Schedule of intangible assets

The following table sets forth the gross carrying amount, accumulated amortization and net carrying amount of our intangible assets as of September 30, 2015 and December 31, 2014:

 

    September 30, 2015
   

 

Gross Carrying Amount

 

 

Accumulated Amortization

 

 Net

Amount

  Weighted- Average Amortization Period (yrs.)
Amortizing intangible assets:                                
   OPERA® software patent   $ 31,951     $ (3,994 )   $ 27,957       14  
   Development costs of                                
      corporate website     91,743       (91,743 )     —         n/a  
   Approved hormone                                
      therapy drug                                
      candidate patents     605,502       (40,199 )     565,303       17.25  
Non-amortizing intangible                                
  assets:                                
   Hormone therapy drug                                
      candidate patents                                
      (pending)     585,241       —         585,241       n/a  
   Multiple trademarks for                                
      vitamins/supplements     145,783       —         145,783       indefinite  
      Total   $ 1,460,220     $ (135,936 )   $ 1,324,284          

 

   

 December 31, 2014

   

 

Gross Carrying Amount

 

 

Accumulated Amortization

 

 Net

Amount

  Weighted- Average Amortization Period (yrs.)
Amortizing intangible assets:                                
   OPERA® software patent   $ 31,951     $ (2,496 )   $ 29,455       14.75  
   Development costs of                                
      corporate website     91,743       (91,743 )     —         n/a  
   Approved hormone                                
      therapy drug                                
      candidate patents     439,184       (19,401 )     419,783       18  
Non-amortizing intangible                                
  assets:                                
   Hormone therapy drug                                
      candidate patents                                
      (pending)     675,982       —         675,982       n/a  
   Multiple trademarks for                                
      vitamins/supplements     103,368       —         103,368       indefinite  
      Total   $ 1,342,228     $ (113,640 )   $ 1,228,588          

 

Schedule of estimated amortization expense

Estimated amortization expense for the next five years is as follows:

 

Year Ending December 31,  Estimated Amortization
 2015 (3 months)   $8,692 
 2016   $34,768 
 2017   $34,768 
 2018   $34,768 
 2019   $34,768 
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INTANGIBLE ASSETS (Details Narrative)
3 Months Ended 9 Months Ended
Sep. 30, 2015
USD ($)
Sep. 30, 2014
USD ($)
Sep. 30, 2015
USD ($)
Sep. 30, 2014
USD ($)
Goodwill and Intangible Assets Disclosure [Abstract]        
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Number of patents 13   13  
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COMMITMENTS AND CONTINGENCIES
9 Months Ended
Sep. 30, 2015
Commitments and Contingencies Disclosure [Abstract]  
COMMITMENTS AND CONTINGENCIES

NOTE 15 – COMMITMENTS AND CONTINGENCIES

 

We lease administrative office space in Boca Raton, Florida pursuant to a 63 month non-cancelable operating lease that commenced on July 1, 2013 and expires on September 30, 2018. On February 18, 2015, we entered into an agreement to lease additional administrative office space in Boca Raton, Florida, pursuant to an addendum to such lease. This addendum was effective beginning April 1, 2015 and will expire with the original lease term on September 30, 2018.

 

The straight line rental expense related to our current lease totaled approximately $119,000 and $90,000 for the three months ended September 30, 2015 and 2014, respectively, and approximately $328,000 and $271,000 for the nine months ended September 30, 2015 and 2014, respectively. The 2014 amounts were partially offset by the rent income of approximately $6,000 and $42,000, respectively, for sublet space. We did not sublet any space during the nine months ended September 30, 2015.

 

As of September 30, 2015, future minimum rental payments are as follows:

 

Years Ending December 31,    
  2015 (3 months)     $ 121,698  
  2016       493,790  
  2017       507,087  
  2018       388,976  
  Minimum lease payments     $ 1,511,551