0000799698-15-000015.txt : 20150803 0000799698-15-000015.hdr.sgml : 20150801 20150803064724 ACCESSION NUMBER: 0000799698-15-000015 CONFORMED SUBMISSION TYPE: 10-Q PUBLIC DOCUMENT COUNT: 11 CONFORMED PERIOD OF REPORT: 20150630 FILED AS OF DATE: 20150803 DATE AS OF CHANGE: 20150803 FILER: COMPANY DATA: COMPANY CONFORMED NAME: CYTRX CORP CENTRAL INDEX KEY: 0000799698 STANDARD INDUSTRIAL CLASSIFICATION: BIOLOGICAL PRODUCTS (NO DIAGNOSTIC SUBSTANCES) [2836] IRS NUMBER: 581642750 STATE OF INCORPORATION: DE FISCAL YEAR END: 1231 FILING VALUES: FORM TYPE: 10-Q SEC ACT: 1934 Act SEC FILE NUMBER: 000-15327 FILM NUMBER: 151020999 BUSINESS ADDRESS: STREET 1: 11726 SAN VICENTE BOULEVARD STREET 2: SUITE 650 CITY: LOS ANGELES STATE: CA ZIP: 90049 BUSINESS PHONE: 310-826-5648 MAIL ADDRESS: STREET 1: 11726 SAN VICENTE BOULEVARD STREET 2: SUITE 650 CITY: LOS ANGELES STATE: CA ZIP: 90049 10-Q 1 form10q022015.htm QUARTER 2, 2015 FORM 10Q form10q022015.htm






UNITED STATES SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549

Form 10-Q

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

For the quarterly period ended June 30, 2015


OR

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

For the transition period from                                                                              to         


Commission file number 0-15327

CytRx Corporation
(Exact name of Registrant as specified in its charter)

Delaware
58-1642740
(State or other jurisdiction of incorporation or organization)
(I.R.S. Employer Identification No.)

11726 San Vicente Blvd., Suite 650
Los Angeles, CA
90049
(Address of principal executive offices)
(Zip Code)

(310) 826-5648
(Registrant’s telephone number, including area code)

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 R     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 during the preceding 12 months (or for such shorter period that the registrant was required to submit and post such files). Yes R  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 R
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 12(b)-2 of the Exchange Act).  Yes £     No R
 
Number of shares of CytRx Corporation common stock, $.001 par value, outstanding as of August 3, 2015: 66,480,065 shares, exclusive of treasury shares.
 


 
 

 



CYTRX CORPORATION

FORM 10-Q

TABLE OF CONTENTS

 
Page
PART I. — FINANCIAL INFORMATION
 
Item 1.    Financial Statements (unaudited)
  1
Item 2.    Management’s Discussion and Analysis of Financial Condition and Results of Operations
  13
Item 3.    Quantitative and Qualitative Disclosures About Market Risk
  18
Item 4.    Controls and Procedures
  18
   
PART II. — OTHER INFORMATION
 
Item 1.    Legal Proceedings
  19
Item 1A.         Risk Factors
  19
Item 6.    Exhibits
  19
   
SIGNATURES
  20
   
INDEX TO EXHIBITS
  21


 
 

 


PART I — FINANCIAL INFORMATION
 
Item 1. — Financial Statements
 
CYTRX CORPORATION
 
CONDENSED BALANCE SHEETS
 
(Unaudited)
 
 
 
June 30,
2015
   
December 31, 2014
 
ASSETS
           
Current assets:
           
Cash and cash equivalents
  $ 38,833,736     $ 32,218,905  
Short-term investments
    15,002,213       45,621,593  
Receivables
    5,175,007       2,019,293  
Interest receivable
    14,196       104,627  
Prepaid expenses and other current assets
    976,325       3,250,355  
Total current assets
    60,001,477       83,214,773  
Equipment and furnishings, net
    879,359       970,873  
Goodwill
    183,780       183,780  
Other assets
    1,569,193       1,323,156  
Total assets
  $ 62,633,809     $ 85,692,582  
LIABILITIES AND STOCKHOLDERS’ EQUITY
               
                 
Current liabilities:
   Accounts payable
  $ 5,328,351     $ 6,655,962  
   Accrued expenses and other current liabilities
    10,376,415       5,994,072  
  Warrant liability
    4,566,515       5,131,085  
   Total current liabilities
    20,271,281       17,781,119  
                 
Commitments and contingencies
               
                 
Stockholders’ equity:
               
Preferred Stock, $0.01 par value, 5,000,000 shares authorized, including 25,000 shares of Series A Junior Participating Preferred Stock; no shares issued and outstanding
           
Common stock, $0.001 par value, 250,000,000 shares authorized;  55,927,197 shares issued and outstanding at June 30, 2015; 55,921,986 shares issued and outstanding at December 31, 2014
    55,927       55,924  
Additional paid-in capital
    380,638,689       376,975,984  
Treasury stock, at cost (199,275 shares)
    (2,612,861 )     (2,612,861 )
Accumulated deficit
    (335,719,227 )     (306,507,584 )
Total stockholders’ equity
    42,362,528       67,911,463  
Total liabilities and stockholders’ equity
  $ 62,633,809     $ 85,692,582  

The accompanying notes are an integral part of these condensed financial statements.


 
-1- 

 

CYTRX CORPORATION
CONDENSED STATEMENTS OF OPERATIONS
(Unaudited)

   
Three Months Ended
June 30,
   
Six Months Ended
June 30,
 
   
2015
   
2014
   
2015
   
2014
 
Revenue:
                       
License revenue
  $     $     $     $  
                                 
Expenses:
                               
Research and development
    10,008,304       10,427,877       22,573,181       17,415,725  
General and administrative
    4,191,769       2,909,127       7,322,001       6,040,201  
      14,200,073       13,337,004       29,895,182       23,455,926  
                                 
Loss before other income (loss)
    (14,200,073 )     (13,337,004 )     (29,895,182 )     (23,455,926 )
                                 
Other income (loss):
                               
Interest income
    46,455       89,377       103,029       160,015  
Other income (loss), net
    30,660       (3,243 )     15,940       6,655  
Gain (loss) on warrant derivative liability
    2,435,865       (2,468,603 )     564,570       12,234,301  
                                 
Net loss
  $ (11,687,093 )   $ (15,719,473 )   $ (29,211,643 )   $ (11,054,955 )
                                 
Basic and diluted net loss per share
  $ (0.21 )   $ (0.28 )   $ (0.52 )   $ (0.21 )
                                 
Basic and diluted weighted-average shares outstanding
    55,726,432       55,676,766       55,724,581       53,010,556  
                                 
                                 

The accompanying notes are an integral part of these condensed financial statements

 
-2-

 


CYTRX CORPORATION
CONDENSED STATEMENTS OF CASH FLOWS
(Unaudited)

   
 
Six Months Ended June 30,
 
 
 
2015
   
2014
 
Cash flows from operating activities:
           
Net loss
  $ (29,211,643 )   $ (11,054,955 )
Adjustments to reconcile net loss to net cash used in operating activities:
               
Depreciation and amortization
    165,830       64,856  
Stock-based compensation expense
    3,662,708       2,627,010  
Fair value adjustment on warrant liability
    (564,570 )     (12,234,301 )
Net foreign exchange loss
          (64 )
Changes in assets and liabilities:
               
Receivables
    (3,155,714 )     (1,480,067 )
Interest receivable
    90,431       (48,929 )
Prepaid expenses and other current assets
    2,027,993       1,410,893  
Accounts payable
    (1,332,633 )     (160,032 )
Accrued expenses and other current liabilities
    4,382,343       3,832,235  
Net cash used in operating activities
    (23,935,255 )     (17,043,354 )
                 
Cash flows from investing activities:
               
Purchase of short-term investments
    (17,960,256 )     (45,601,506 )
Proceeds from the sale of short-term investments
    48,579,636       22,084,980  
Purchases of equipment and furnishings
    (69,294 )     (20,733 )
Net cash provided by (used in) investing activities
    30,550,086       (23,537,259 )
                 
Cash flows from financing activities:
   Net proceeds from public offering
          80,535,401  
   Proceeds from issuance of restricted stock to employee
          100  
   Net proceeds from exercise of warrants and stock options
          428,891  
Net cash provided by financing activities
          80,964,392  
                 
Net increase in cash and cash equivalents
    6,614,831       40,383,779  
Cash and cash equivalents at beginning of period
    32,218,905       11,483,112  
Cash and cash equivalents at end of period
  $ 38,833,736     $ 51,866,891  
                 
Supplemental disclosure of cash flow information:
               
                 
Equipment and furnishings purchased on credit
  $ 5,022     $ 107,506  
                 
Cashless warrant exercises
  $ 3     $ 133  
                 
Cash paid for income taxes
  $ 800     $ 59,431  


The accompanying notes are an integral part of these condensed financial statements.


 

 
-3- 

 

NOTES TO CONDENSED FINANCIAL STATEMENTS
 
June 30, 2015
 
(Unaudited)
 
1.  Description of Company and Basis of Presentation
 
CytRx Corporation (“CytRx” or the “Company”) is a biopharmaceutical research and development company specializing in oncology. The Company is currently focused on the clinical development of aldoxorubicin (formerly known as INNO-206), its modified version of the widely-used chemotherapeutic agent, doxorubicin. CytRx previously reported positive top-line efficacy results (median progression-free survival, or PFS, PFS at six months, overall response rates, hazard ratios and overall survival) from its completed, global Phase 2b clinical trial with aldoxorubicin as a treatment for soft tissue sarcoma, or STS. Hazard ratios, or the likelihood that the study endpoint (in this case tumor progression) will be reached during a given period, are an important measure of the reliability and uniformity of the absolute data for PFS. The trial investigated the efficacy and safety of aldoxorubicin compared with doxorubicin in subjects with first-line metastatic, locally advanced or unresectable STS. Aldoxorubicin combines the chemotherapeutic agent doxorubicin with a novel linker-molecule that binds specifically to albumin in the blood and is designed to allow for delivery of higher amounts of doxorubicin (3½ to 4 times) without the major dose-limiting toxicities as seen with the administration of doxorubicin alone.
 
In the first quarter of 2014, the Company initiated a pivotal Phase 3 trial of aldoxorubicin as a therapy for patients with STS whose tumors have progressed following treatment with chemotherapy. The Phase 3 trial is being conducted under a Special Protocol Assessment, or SPA, granted by the FDA. The SPA means that the FDA agrees that the design and analyses proposed in the Phase 3 trial protocol are acceptable to support regulatory approval of the product candidate with respect to effectiveness of the indication studied, and will not change its perspective on these matters, except in limited circumstances such as where a sponsor fails to follow a protocol agreed to with the FDA or where previously unrecognized health concerns occur.  Thus, if the study demonstrates an acceptable benefit-risk profile as determined by the FDA, it will support registration of aldoxorubicin for this indication.  If approved for marketing, the Company’s current plan would be to commercially launch aldoxorubicin in late 2017.
 
CytRx is currently evaluating aldoxorubicin in a global Phase 2b clinical trial in small cell lung cancer, a Phase 2 clinical trial in HIV-related Kaposi's sarcoma, a Phase 2 clinical trial in patients with late-stage glioblastoma (brain cancer), a Phase 1b clinical trial in combination with ifosfamide in patients with STS and a Phase 1b clinical trial in combination with gemcitabine in patients with metastatic solid tumors. The Company has completed a global Phase 2b clinical trial with aldoxorubicin as a 1st-line therapy for STS, a Phase 1b/2 clinical trial primarily in the same indication, a Phase 1b clinical trial of aldoxorubicin in combination with doxorubicin in patients with advanced solid tumors and a Phase 1b pharmacokinetics clinical trial in patients with metastatic solid tumors.
 
CytRx plans to expand its pipeline of oncology candidates through its drug-development activities at its laboratory facility in Freiburg, Germany, based on its Linker Activated Drug Release, or LADR™, technology that can be utilized with multiple chemotherapeutic agents and may allow for greater drug concentration at tumor sites.
 
The accompanying condensed financial statements at June 30, 2015 and for the three-month and six-month periods ended June 30, 2015 and 2014, respectively, are unaudited, but include all adjustments, consisting of normal recurring entries, that management believes to be necessary for a fair presentation of the periods presented. Interim results are not necessarily indicative of results for a full year. Balance sheet amounts as of December 31, 2014 have been derived from the Company’s audited financial statements as of that date.
 
The financial statements included herein have been prepared by the Company pursuant to the rules and regulations of the Securities and Exchange Commission (“SEC”). Certain information and footnote disclosures normally included in financial statements prepared in accordance with accounting principles generally accepted in the United States of America have been condensed or omitted pursuant to such rules and regulations. The financial statements should be read in conjunction with the Company’s audited financial statements contained in its Annual Report on Form 10-K for the year ended December 31, 2014. The Company’s operating results will fluctuate for the foreseeable future. Therefore, period-to-period comparisons should not be relied upon as predictive of the results in future periods.
 
2.           Recent Accounting Pronouncements
 
We have reviewed all of the recent accounting pronouncements and have determined that they have not or will not have a material impact on the Company’s financial statements, or simply do not apply to the Company’s operations.
 

 
-4- 

 
3.           Foreign Currency Remeasurement
 
The U.S. dollar has been determined to be the functional currency for the net assets of the Company’s laboratory facility in Germany. The transactions are recorded in the local currencies and are remeasured at each reporting date using the historical rates for nonmonetary assets and liabilities and exchange rates for monetary assets and liabilities at the balance sheet date. Exchange gains and losses from the remeasurement of monetary assets and liabilities are recognized in other income (loss). The Company recognized a gain of approximately $5,000 and a loss of approximately $10,700 for the three-month and six-month periods ended June 30, 2015, respectively, and $0 and $4,900 for the three and six-month periods ended June 30, 2014, respectively.
 
4.           Short-term Investments
 
The Company held $15.0 million of short-term investments at June 30, 2015, as compared to $45.6 million at December 31, 2014.  The Company has classified these investments as available for sale.  These investments are federally insured certificates of deposit with a maturity date of August 27, 2015.
 
5.           Basic and Diluted Net Loss Per Common Share
 
Basic and diluted net loss per common share is computed based on the weighted-average number of common shares outstanding. Common share equivalents (which consist of options, warrants and restricted stock) are excluded from the computation of diluted net loss per common share where the effect would be anti-dilutive.  Common share equivalents that could potentially dilute net loss per share in the future, and which were excluded from the computation of diluted loss per share, totaled 17.8 million shares for each of the three-month and six-month periods ended June 30, 2015, and 14.6 million shares for each of the three-month and six-month periods ended June 30, 2014.
 
6.           Warrant Liabilities
 
Liabilities measured at fair value on a recurring basis include warrant liabilities resulting from the Company’s past equity financings.  In accordance with ASC 815-40, Derivatives and Hedging – Contracts in Entity’s Own Equity (“ASC 815-40”), the warrant liabilities are being recorded at fair value until they are completely settled.  The warrants are valued using the Black-Scholes method, using assumptions consistent with the Company’s application of ASC 505-50, Equity-Based Payments to Non-Employees (“ASC 505-50”).  The gain or loss resulting from the change in fair value is shown on the Condensed Statements of Operations as gain (loss) on warrant derivative liability. The Company recognized a gain (loss) of $2.4 million and ($2.5) million for the three-month periods ended June 30, 2015 and 2014, respectively, and a gain of $0.6 million and $12.2 million for the six-month periods ended June 30, 2015 and 2014, respectively. The following reflects the weighted-average assumptions for each of the six-month periods indicated:
 
   
Six Months Ended June 30,
 
 
 
2015
   
2014
 
             
Risk-free interest rate
    0.28 %     0.44 %
Expected dividend yield
    0 %     0 %
Expected lives
    1.09       1.96  
    Expected volatility
    62.7 %     84.1 %
    Warrants classified as liabilities (in shares)
    6,371,854       6,984,716  
 
The Company’s computation of expected volatility is based on the historical daily volatility of its publicly traded stock. The dividend yield assumption of zero is based upon the fact that the Company has never paid cash dividends and presently has no intention to do so.  The risk-free interest rate used for each warrant classified as a derivative is equal to the U.S. Treasury rates in effect at June 30 of each year presented. The expected lives are based on the remaining contractual lives of the related warrants at the valuation date.
 
7.           Stock Based Compensation
 
The Company has a 2000 Long-Term Incentive Plan, which expired on August 6, 2010.  As of June 30, 2015, there were approximately 0.6 million shares subject to outstanding stock options under this plan.  No further shares are available for future grant under this plan.
 
The Company also has a 2008 Stock Incentive Plan.  As of June 30, 2015, there were 9.9 million shares subject to outstanding stock options and 10.1 million shares available for future grant under this plan.
 

 
-5- 

 

The Company follows ASC 718, Compensation-Stock Compensation, which requires the measurement and recognition of compensation expense for all stock-based awards made to employees.
 
For stock options and stock warrants paid in consideration of services rendered by non-employees, the Company recognizes compensation expense in accordance with the requirements of ASC 505-50.
 
Non-employee option grants that do not vest immediately upon grant are recorded as an expense over the vesting period. At the end of each financial reporting period, the value of these options, as calculated using the Black-Scholes option-pricing model, is determined, and compensation expense recognized or recovered during the period is adjusted accordingly. As a result, the amount of the future compensation expense is subject to adjustment until the common stock options are fully vested.
 
The following table sets forth the total stock-based compensation expense resulting from stock options and warrants included in the Company’s unaudited interim statements of operations:
 
   
Three Months Ended June 30,
   
Six Months Ended June 30,
 
   
2015
   
2014
   
2015
   
2014
 
Research and development — employee
  $ 392,842     $ 234,484     $ 728,780     $ 409,638  
General and administrative — employee
    1,744,440       325,379       2,699,844       637,339  
Total employee stock-based compensation
  $ 2,137,282     $ 559,863     $ 3,428,624     $ 1,046,977  
                                 
Research and development — non-employee
  $     $     $     $  
General and administrative — non-employee
    140,533       160,629       234,084       352,620  
 Total non-employee stock-based compensation
  $ 140,533     $ 160,629     $ 234,084     $ 352,620  

During the six-month period ended June 30, 2015, the Company granted stock options to purchase 550,000 shares of its common stock. During the six-month period ended June 30, 2014, the Company granted stock options to purchase 300,000 shares of its common stock and issued warrants to purchase 25,000 shares of its stock with an exercise price of $5.60.The fair value of the stock options was estimated using the Black-Scholes option-pricing model, based on the following assumptions:
 
 
 
Six Months Ended June 30, 2015
   
Six Months Ended June 30, 2014
 
Risk-free interest rate
    2.21 %     1.92 %
Expected volatility
    78.2% - 84.4 %     87.0% - 89.6 %
Expected lives (years)
    6 - 10       6 - 10  
Expected dividend yield
    0.00 %     0.00 %
 
The Company’s computation of expected volatility is based on the historical daily volatility of its publicly traded stock.  The Company uses historical information to compute expected lives. In the six-month period ended June 30, 2015, the contractual term of the options granted was ten years. The dividend yield assumption of zero is based upon the fact the Company has never paid cash dividends and presently has no intention to do so.  The risk-free interest rate used for each grant and issuance is equal to the U.S. Treasury rates in effect at the time of the grant and issuance for instruments with a similar expected life. Based on historical experience, for the six-month period ended June 30, 2015, the Company estimated annualized forfeiture rates of 10% for options granted to its employees, 2% for options granted to senior management and 0% for options granted to directors and non-employees and for warrants issued to non-employees.  For the six-month period ended June 30, 2014, the Company estimated annualized forfeiture rates of 12% for options granted to its employees, 2% for options granted to senior management and 0% for options granted to directors and non-employees.  Compensation costs will be adjusted for future changes in estimated forfeitures.  The Company will record additional expense if the actual forfeitures are lower than estimated and will record a recovery of prior expense if the actual forfeiture rates are higher than estimated.
 
 
-6- 

 
As of June 30, 2015, there remained approximately $4.9 million of unrecognized compensation expense related to unvested stock options granted to current and former employees, directors, to be recognized as expense over a weighted-average period of 1.03 years. Presented below is the Company’s stock option activity:
 
 
 
Six Months Ended June 30, 2015
 
 
 
 
Number of Options (Employees)
   
Number of Options (Non-Employees)
   
Total Number
of Options
   
Weighted-Average Exercise Price
 
Outstanding at January 1, 2015
    9,348,952       692,143       10,040,735     $ 2.87  
Granted
    550,000             550,000     $ 3.86  
Expired
    (68,000 )     (56,429 )     (124,429 )   $ 6.90  
Outstanding at June 30, 2015
    9,830,952       635,714       10,466,306     $ 3.33  
Options exercisable at June 30, 2015
    6,276,275       635,714       6,911,989     $ 3.59  


The following table summarizes significant ranges of outstanding stock options under the Company’s plans at June 30, 2015:

Range of
 Exercise Prices
   
Total Number
of Options
   
Weighted-Average Remaining Contractual Life (years)
   
Weighted-Average Exercise Price
   
Total Number of Options Exercisable
   
Weighted-Average Remaining Contractual Life (years)
   
Weighted-Average Exercise Price
 
$ 1.83 - $2.50       5,837,558       8.51     $ 2.12       3,226,398       8.00     $ 2.08  
$ 2.51 – $3.50       954,482       8.64     $ 2.85       874,482       8.62     $ 2.83  
$ 3.51 – $8.00       3,386,201       7.93     $ 5.06       2,523,043       7.74     $ 5.16  
$ 8.01 – $32.55       288,065       2.31     $ 9.00       288,066       2.31     $ 9.00  
          10,466,306       8.16     $ 3.33       6,911,989       7.74     $ 3.59  

The aggregate intrinsic value of all outstanding options and vested options as of June 30, 2015 was $10.2 million and $6.1 million, respectively, representing options with exercise prices of less than the closing fair market value of the Company’s common stock on June 30, 2015 of $3.72 per share.
 
There were 7,282,617 and 7,349,760 warrants outstanding at June 30, 2015 and December 31, 2014, respectively at a weighted-average exercise price of $4.29 and $4.27, respectively.
 
Restricted Stock
 
On January 1, 2014, the Company granted to Dr. Daniel Levitt, Executive Vice President and Chief Medical Officer, 100,000 shares of CytRx Corporation restricted stock pursuant to the 2008 Plan, which shares have now fully vested.  The fair value of the restricted stock is based on the market price of the Company’s shares on the grant date less the par value received as consideration. The fair value of the restricted shares granted on January 1, 2014 was $627,000. The stock-based compensation expense relating to restricted stock included in the Company’s unaudited statements of operations for the three-month and six-month periods ended  June 30, 2014 was $156,296 and $310,874, respectively.  No restricted shares of common stock of the Company were granted in the comparable periods in 2015.
 
 
-7- 

 
8.           Fair Value Measurements
 
Assets and liabilities recorded at fair value on the balance sheets are categorized based upon the level of judgment associated with the inputs used to measure the fair value.  Level inputs are as follows:
 
Level 1 – quoted prices in active markets for identical assets or liabilities.
 
 
Level 2 – other significant observable inputs for the assets or liabilities through corroboration with market data at the measurement date.
 
 
Level 3 – significant unobservable inputs that reflect management’s best estimate of what market participants would use to price the assets or liabilities at the measurement date.
 
The following table summarizes fair value measurements by level at June 30, 2015 for assets and liabilities measured at fair value on a recurring basis:
 
(In thousands)
 
Level I
   
Level II
   
Level III
   
Total
 
Cash equivalents
  $ 38,437     $     $     $ 38,437  
Short-term investments
    15,002                   15,002  
Warrant liabilities
                (4,567 )     (4,567 )

The following table summarizes fair value measurements by level at December 31, 2014 for assets and liabilities measured at fair value on a recurring basis:
 
(In thousands)
 
Level I
   
Level II
   
Level III
   
Total
 
Cash equivalents
  $ 31,159     $     $     $ 31,159  
Short-term investments
    45,622                   45,622  
Warrant liability
                (5,131 )     (5,131 )

Liabilities measured at market value on a recurring basis include warrant liability resulting from the Company’s August 2011 equity financing. In accordance with ASC 815-40, the warrant liability are marked to market each quarter-end until they are completely settled. The warrants are valued using the Black-Scholes method, using assumptions consistent with the Company’s application of ASC 505-50. The change in the fair value of the liabilities classified in Level III is due to the unrealized gain of $0.6 million recognized and the gain is presented in the Condensed Statement of Operations (see Note 6).
 
The Company considers carrying amounts of accounts receivable, accounts payable and accrued expenses to approximate fair value due to the short-term nature of these financial instruments.  
 
The Company’s non-financial assets are measured at fair value when there is an indicator of impairment and recorded at fair value only when an impairment charge is recognized.  The Company’s non-financial assets were not material at June 30, 2015 or 2014.
 
9.           Liquidity and Capital Resources
 
At June 30, 2015, the Company had cash and cash equivalents of approximately $38.8 million and short-term investments of approximately $15.0 million.  Management believes that the Company’s current cash and cash equivalents and short-term investments, along with the $26.8 million of net proceeds received from our underwritten public offering on July 21, 2015 (see Note 13), will be sufficient to fund its operations for the foreseeable future.  The estimate is based, in part, upon the Company’s currently projected expenditures for the remainder of 2015 and the first six months of 2016 of approximately $53.1 million, which includes approximately $36.1 million for its clinical programs for aldoxorubicin, approximately $2.3 million for pre-clinical development of new albumin-binding cancer drug candidates, approximately $3.9 million for general operation of its clinical programs, and approximately $10.8 million for other general and administrative expenses (including pre-commercialization). These projected expenditures are also based upon numerous other assumptions and subject to many uncertainties, and the Company’s actual expenditures may be significantly different from these projections.
 
If the Company obtains marketing approval and successfully commercializes aldoxorubicin or other product candidates, the Company anticipates it could take several years, for it to generate significant recurring revenue.  The Company will be dependent on future financing and possible strategic partnerships until such time, if ever, as it can generate significant recurring revenue. The Company has no commitments from third parties to provide any additional financing, and it may not be able to obtain future financing on favorable terms, or at all. If the Company fails to obtain sufficient funding when needed, it may be forced to delay, scale back or eliminate all or a portion of its development programs or clinical trials, seek to license to other companies its product candidates or technologies that it would prefer to develop and commercialize itself, or seek to sell some or all of its assets or merge with or be acquired by another company.
 
 
-8- 

 
10.           Equity Transactions
 
On April 27, 2015, the Company issued 5,211 common shares pursant to a net exercise of warrants to purchase 10,000 shares.
 
On January 1, 2014, the Company granted 100,000 shares of restricted stock to Dr. Daniel Levitt, Executive Vice President and Chief Medical Officer (see Note 7), which resulted in non-cash expense of $0.6 million.
 
On February 5, 2014, the Company completed an $86.0 million underwritten public offering, in which it sold and issued 13.2 million shares of common stock at a price of $6.50 per share. Net of underwriting discounts, legal, accounting and other offering expenses, the Company received proceeds of approximately $80.5 million.
 
On March 15, 2014, the Company issued 200,000 common shares and warrants to purchase 25,000 common shares to KTB Tumorforschungs GmbH, or “KTB,” the licensor of aldoxorubicin, in connection with the establishment of the Company’s Freiburg, Germany research and development laboratory. The fair value of the shares was $0.8 million.
 
In the first quarter of 2014, the Company issued approximately 278,000 common shares for $0.4 million pursuant to the exercise of warrants.
 
11.           Income Taxes
 
At December 31, 2014, the Company had federal and state net operating loss carryforwards as of  $227.5 million and $157.5 million, respectively, available to offset against future taxable income, and which expire in 2015 through 2034. Of such loss carryforwards, $165.2 million and $157.5 million, respectively, are not subject to limitation under Section 382 of the Internal Revenue Code.
 
12.           Commitments and Contingencies
 
Commitments
 
The Company has an agreement with KTB for the Company’s exclusive license of patent rights held by KTB for the worldwide development and commercialization of aldoxorubicin. Under the agreement, the Company must make payments to KTB in the aggregate of $7.5 million upon meeting clinical and regulatory milestones up to and including the product’s second final marketing approval. In the six months ended June 30, 2014, the Company met two clinical milestones, resulting in total payments of $2.0 million to KTB.  The Company also has agreed to pay:
 
·  
commercially reasonable royalties based on a percentage of net sales (as defined in the agreement);
 
·  
a percentage of non-royalty sub-licensing income (as defined in the agreement); and
 
·  
milestones of $1 million for each additional final marketing approval that the Company obtains.
 
In the event that the Company must pay a third party in order to exercise its rights to the intellectual property under the agreement, the Company will deduct a percentage of those payments from the royalties due KTB, up to an agreed upon cap.
 
 
-9- 

 
Contingencies
 
On June 13, 2014, three purported securities class action lawsuits pending in the United States District Court for the Central District of California, were consolidated in the matter of In re CytRx Corporation Securities Litigation, 2:14-CV-01956-GHK (PJWx), and lead plaintiff and lead counsel were appointed. On October 1, 2014, plaintiffs filed a consolidated amended complaint on behalf of all persons who purchased or otherwise acquired the publicly traded securities of CytRx between November 20, 2013 and March 13, 2014, against CytRx, certain Company officers and directors, a freelance writer, and certain underwriters. The complaint alleges that certain of the defendants violated the Securities Exchange Act of 1934 by making materially false and misleading statements in press releases, promotional articles, SEC filings and other public statements. The complaint further alleges that certain of the defendants violated the Securities Act of 1933 by making materially misleading statements and omitting material information in the shelf Registration Statement on Form S-3 filed with the SEC on December 6, 2012 and Prospectus Supplement on Form 424(b)(2) filed with the SEC on January 31, 2014. These allegations arise out of the Company’s alleged retention of The DreamTeam Group and MissionIR, external investor and public relations firms unaffiliated with the Company, as well as the Company’s December 9, 2013 grant of stock options to certain board members and officers. The consolidated amended complaint seeks damages, including interest, in an unspecified amount, reasonable costs and attorneys’ fees, and any equitable, injunctive, or other relief that the court may deem just and proper.  On December 5, 2014, CytRx and the individual defendants filed a motion to dismiss the complaint.  The Court was scheduled to hear argument on this motion on March 2, 2015.  On February 25, 2015, the Court took this motion under submission and took the hearing off calendar. On July 13, 2015, the Court issued an order granting in part and denying in part the motions to dismiss filed by us, the individual defendants and the underwriters. The Court afforded the plaintiffs 30 days to amend their complaint, if they elect to do so.
 
    On April 3, 2014, a purported class action lawsuit was filed against the Company and certain of its officers and each of its directors, as well as certain underwriters, in the Superior Court of California, County of Los Angeles, captioned Rajasekaran v. CytRx Corporation, et al., BC541426. The complaint purports to be brought on behalf of all shareholders who purchased or otherwise acquired the Company’s common stock pursuant or traceable to its public offering that closed on February 5, 2014. The complaint alleges that defendants violated the federal securities laws by making materially false and misleading statements in the Company’s filings with the SEC. The complaint seeks compensatory damages in an unspecified amount, rescission, and attorney’s fees and costs. On October 14, 2014, the Court granted the parties’ joint ex parte motion to stay this proceeding pending resolution of motions to dismiss in the related federal action,  In re CytRx Corporation Securities Litigation , 2:14-CV-01956-GHK (PJWx).
 
    On July 3, 2014, a shareholder derivative lawsuit was filed in the United States District Court for the Central District of California, captioned  Fishman v. Kriegsman, et al. , 2:14-cv-05169, purportedly on the Company’s behalf against certain of its officers and each of its directors. The complaint alleges breach of fiduciary duties, corporate waste, gross mismanagement, and unjust enrichment in connection with the Company’s alleged retention of DreamTeamGroup and MissionIR. The complaint seeks damages, restitution, corporate governance reforms, and attorney’s fees and costs. On September 3, 2014, plaintiff filed a notice to voluntarily dismiss this action against all parties without prejudice, which the Court granted on September 9, 2014.
 
    On September 10, 2014, the Delaware Court of Chancery consolidated Schwartz v. Ignarro, et al., Case No. 9864, Johnson v. Ignarro, et al. , Case No. 9884, and  Silverberg v. Kriegsman, et al. , Case No. 9919, three shareholder derivative lawsuits described in the Company’s Quarterly Report filed with the SEC on August 6, 2014. The allegations in the  Schwartz  and  Johnson complaints relate to the Company’s December 9, 2013 grant of stock options to certain board members and officers. The allegations in the  Silverberg  complaint relate to the Company’s December 9, 2013 grant of stock options to certain board members and officers, as well as its alleged retention of DreamTeamGroup and MissionIR. A consolidated complaint concentrated on the stock-option grant claims was filed on October 9, 2014. The consolidated lawsuit is captioned  In re CytRx Corp. Stockholder Derivative Litigation,  C.A. No. 9864-VCL. On November 10, 2014, the Company and the individual defendants filed a motion to dismiss the consolidated complaint or, in the alternative, to stay the action. The Court heard argument on the motions on January 8, 2015. The Court denied the motion to dismiss and granted in part and denied in part the motion to stay.
 
 
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    On June 2, 2015, the Company announced that they had reached an agreement to settle the Delaware stockholder derivative action. Under the settlement, it agreed to re-price certain stock options to purchase common stock that were granted on December 10, 2013 to certain of its directors and officers from the original exercise price of $2.39 to an exercise price of $4.66 (the share price at market closing on December 20, 2013). The settlement also provides that the Company will implement certain corporate governance changes and modify its governance practices regarding the granting of stock options. The parties have reached an agreement on an award of $1.1 million of fees and expenses to plaintiffs’ attorneys, which award must be approved by the Court regardless of whether there is an agreement between the parties. These fees and expenses will be covered by the Company’s insurance companies. The settlement is subject to the drafting of definitive documentation, notice to stockholders, and Court approval.
 
    On August 14, 2014, a shareholder derivative lawsuit, captioned Pankratz v. Kriegsman, et al., 2:14-cv-06414-PA-JPR, was filed in the United States District Court for the Central District of California purportedly on the Company’s behalf against certain of its officers and each of its directors. The complaint alleges breach of fiduciary duties, unjust enrichment, gross mismanagement, abuse of control, insider selling and misappropriation of information in connection with the Company’s alleged retention of DreamTeamGroup and MissionIR, as well as its December 9, 2013 grant of stock options to certain board members and officers. The complaint seeks unspecified damages, corporate governance and internal procedures reforms, restitution, disgorgement of all profits, benefits, and other compensation obtained by the individual defendants, and the costs and disbursements of the action.
 
    On August 15, 2014, a shareholder derivative complaint, captioned Taylor v. Kriegsman, et al., 2:14-cv-06451, was filed in the United States District Court for the Central District of California purportedly on the Company’s behalf against certain of its officers and each of its directors. The complaint alleges breach of fiduciary duties, unjust enrichment, gross mismanagement, abuse of control, unjust enrichment, insider selling and misappropriation of information in connection with the Company’s alleged retention of DreamTeamGroup and MissionIR, as well as its December 9, 2013 grant of stock options to certain board members and officers. The complaint seeks unspecified damages, corporate governance and internal procedures reforms, restitution, disgorgement of all profits, benefits, and other compensation obtained by the individual defendants, and the costs and disbursements of the action.
 
    On October 8, 2014, the Court in Pankratz and Taylor consolidated the cases and appointed lead plaintiffs and co-lead counsel. On October 20, 2014, the Company and the individual defendants filed motions to dismiss the consolidated  Pankratz  and Taylor  cases or, in the alternative, to stay the cases. On January 9, 2015, the Court stayed the action pending the resolution of the consolidated Delaware derivative action. On February 27, 2015, the  Pankratz  and  Taylor  plaintiffs filed a motion to vacate the stay. On June 24, 2015, the Court granted the motion to lift the stay in light of the pending settlement of the Delaware derivative litigation discussed above. The Court further denied the motion to dismiss without prejudice and invited the Company to move to dismiss the case within 30 days pursuant to the doctrine of  forum non conveniens  based on its forum-selection bylaw, which mandates that derivative actions be filed in Delaware. The Court advised that it would consider any  forum non conveniens  motion before considering a subsequent motion to dismiss under Rule 12.

    The Company intends to vigorously defend against the foregoing complaints. The Company has directors’ and officers’ liability insurance, which will be utilized in the defense of these matters. The Company has incurred legal expenses in defending these complaints and as of June 30, 2015, the Company has an outstanding receivable from its insurance carrier of $5.2 million related to these expenses. The liability insurance may not cover all of the future liabilities the Company may incur in connection with the foregoing matters. These claims are subject to inherent uncertainties, and managements’s views of these matters may change in the future.

    The Company evaluates developments in legal proceedings and other matters on a quarterly basis. If an unfavorable outcome becomes probable and reasonably estimable, the Company could incur charges that could have a material adverse impact on the Comapny’s financial condition and results of operations for the period in which the outcome becomes probable and reasonably estimable.
 
 
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13. Subsequent Events
 
On July 24, 2015, the Company completed a $28.7 million underwritten public offering, in which it sold and issued 10,465,000 shares of common stock at a price of $2.75 per share. Net of underwriting discounts, legal, accounting and other offering expenses, the Company received proceeds of approximately $26.8 million, exclusive of treasury shares.
 
The following selected pro forma balance sheet data is derived from our balance sheet as of June 30, 2015 and gives retroactive effect to the completion of the underwritten offering, but does not give effect to other events that occurred since June 30, 2015  and thus may not be indicative of our current financial condition. The information should be read in conjunction with our balance sheet as of June 30, 2015  and related notes.
 
   
Actual as of June 30, 2015 (unaudited)
   
Adjustments Related to July 2015 Equity Financing (unaudited)
   
Pro Forma as of June 30, 2015 (unaudited)
 
ASSETS
                 
                   
Current assets:
                 
Cash and cash equivalents
  $ 38,833,736     $ 26,752,025     $ 65,585,761  
Short-term investments
    15,002,213             15,002,213  
Prepaid and other current assets
    6,165,528             6,165,528  
    Total current assets
    60,001,477       26,752,025       86,753,502  
Non-current assets
    2,632,332             2,632,332  
Total assets
  $ 62,633,809     $ 26,752,025     $ 89,385,834  
                         
LIABILITIES AND STOCKHOLDERS’ EQUITY
                       
                         
Current liabilities:                        
     Accounts payable and other current liabilities                    $ 15,704,766            $ 15,704,766   
     Warrant liability   $     4,566,515             $ 4,566,515   
Total current liabilities
  $ 20,271,281     $     $ 20,271,281  

Stockholders’ equity:
                 
                   
 Common stock
  $ 55,927     $ 10,465     $ 66,392  
   Additional paid-in-capital
    380,638,689       26,741,560       407,380,249  
   Treasury stock
    (2,612,861 )           (2,612,861 )
   Accumulated deficit
    (335,719,227 )           (335,719,227 )
Total stockholders’ equity
    42,362,528       26,752,025       69,114,553  
Total liabilities and stockholders’ equity
  $ 62,633,809     $ 26,752,025     $ 89,385,834  

 
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Item 2. — Management’s Discussion and Analysis of Financial Condition and Results of Operations
 
Forward Looking Statements
 
From time to time, we make oral and written statements that may constitute “forward-looking statements” (rather than historical facts) as defined in the Private Securities Litigation Reform Act of 1995 or by the SEC in its rules, regulations and releases, including Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended. We desire to take advantage of the “safe harbor” provisions in the Private Securities Litigation Reform Act of 1995 for forward-looking statements made from time to time, including, but not limited to, the forward-looking statements made in this Quarterly Report, as well as those made in our other filings with the SEC.
 
All statements in this Quarterly Report, including statements in this section, other than statements of historical fact are forward-looking statements for purposes of these provisions, including statements of our current views with respect to the recent developments regarding our business strategy, business plan and research and development activities, our future financial results, and other future events. These statements include forward-looking statements both with respect to us, specifically, and the biotechnology industry, in general. In some cases, forward-looking statements can be identified by the use of terminology such as “may,” “will,” “expects,” “plans,” “anticipates,” “estimates,” “potential” or “could” or the negative thereof or other comparable terminology. Although we believe that the expectations reflected in the forward-looking statements contained herein are reasonable, there can be no assurance that such expectations or any of the forward-looking statements will prove to be correct, and actual results could differ materially from those projected or assumed in the forward-looking statements.
 
All forward-looking statements involve inherent risks and uncertainties, and there are or will be important factors that could cause actual results to differ materially from those indicated in these statements. We believe that these factors include, but are not limited to, the factors discussed in this section and under the caption “Risk Factors” in our Annual Report on Form 10-K for the year ended December 31, 2014, which should be reviewed carefully. If one or more of these or other risks or uncertainties materialize, or if our underlying assumptions prove to be incorrect, actual results may vary materially from what we anticipate. Please consider our forward-looking statements in light of those risks as you read this Quarterly Report. We undertake no obligation to publicly update or review any forward-looking statement, whether as a result of new information, future developments or otherwise.
 
Overview
 
CytRx Corporation (“CytRx” or the “Company,we, us, our”) is a biopharmaceutical research and development company specializing in oncology. We are currently focused on the clinical development of aldoxorubicin (formerly known as INNO-206), our modified version of the widely-used chemotherapeutic agent, doxorubicin. We previously reported positive top-line efficacy results (median progression-free survival, or PFS, PFS at six months, overall response rates, hazard ratios and overall survival) from our completed, global Phase 2b clinical trial with aldoxorubicin as a treatment for soft tissue sarcoma, or STS. Hazard ratios, or the likelihood that the study endpoint (in this case tumor progression) will be reached during a given period, are an important measure of the reliability and uniformity of the absolute data for PFS. The trial investigated the efficacy and safety of aldoxorubicin compared with doxorubicin in subjects with first-line metastatic, locally advanced or unresectable STS. Aldoxorubicin combines the chemotherapeutic agent doxorubicin with a novel linker-molecule that binds specifically to albumin in the blood and is designed to allow for delivery of higher amounts of doxorubicin (3½ to 4 times) without the major dose-limiting toxicities as seen with the administration of doxorubicin alone.
 
In the first quarter of 2014, we initiated a pivotal Phase 3 trial of aldoxorubicin as a therapy for patients with STS whose tumors have progressed following treatment with chemotherapy. The Phase 3 trial is being conducted under a Special Protocol Assessment, or SPA, granted by the FDA. The SPA means that the FDA agrees that the design and analyses proposed in the Phase 3 trial protocol are acceptable to support regulatory approval of the product candidate with respect to effectiveness of the indication studied, and will not change its perspective on these matters, except in limited circumstances such as where a sponsor fails to follow a protocol agreed to with the FDA or where previously unrecognized health concerns occur.  Thus, if the study demonstrates an acceptable benefit-risk profile as determined by the FDA, it will support registration of aldoxorubicin for this indication.  If approved for marketing, our current plan would be to commercially launch aldoxorubicin in late 2017.
 
We are currently evaluating aldoxorubicin in a global Phase 2b clinical trial in small cell lung cancer, a Phase 2 clinical trial in HIV-related Kaposi's sarcoma, a Phase 2 clinical trial in patients with late-stage glioblastoma (brain cancer), a Phase 1b clinical trial in combination with ifosfamide in patients with STS and a Phase 1b clinical trial in combination with gemcitabine in patients with metastatic solid tumors. We have completed a global Phase 2b clinical trial with aldoxorubicin as a 1st-line therapy for STS, a Phase 1b/2 clinical trial primarily in the same indication, a Phase 1b clinical trial of aldoxorubicin in combination with doxorubicin in patients with advanced solid tumors and a Phase 1b pharmacokinetics clinical trial in patients with metastatic solid tumors.
 
We plan to expand our pipeline of oncology candidates through our drug-development activities at our laboratory facility in Freiburg, Germany, based on our Linker Activated Drug Release, or LADR™, technology that can be utilized with multiple chemotherapeutic agents and may allow for greater drug concentration at tumor sites.
 
 
 
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Critical Accounting Policies and Estimates
 
Management’s discussion and analysis of our financial condition and results of operations are based on our financial statements, which have been prepared in accordance with accounting principles generally accepted in the U.S. The preparation of these financial statements requires management to make estimates and judgments that affect the reported amounts of assets, liabilities, revenue and expenses, and related disclosure of contingent assets and liabilities. On an ongoing basis, management evaluates its estimates, including those related to revenue recognition, impairment of long-lived assets, including finite-lived intangible assets, research and development expenses and clinical trial expenses and stock-based compensation expense.
 
We base our estimates on historical experience and on various other assumptions that are believed to be reasonable under the circumstances, the results of which form the basis for making judgments about the carrying values of assets and liabilities that are not readily apparent from other sources. Actual results may differ materially from these estimates under different assumptions or conditions.
 
Our significant accounting policies are summarized in Note 2 to our financial statements contained in our Annual Report on Form 10-K for the year ended December 31, 2014. We believe the following critical accounting policies affect our more significant judgments and estimates used in the preparation of our financial statements.
 
Revenue Recognition
 
Revenue consists of license fees from strategic alliances with pharmaceutical companies, as well as service and grant revenues. Service revenue consists of contract research and laboratory consulting. Grant revenues consist of government and private grants.
 
Monies received for license fees are deferred and recognized ratably over the performance period in accordance with  Financial Accounting Standards Board (“FASB”) Accounting Codification Standards (“ASC”) ASC 605-25, Revenue Recognition – Multiple-Element Arrangements (“ASC 605-25”). Milestone payments will be recognized upon achievement of the milestone as long as the milestone is deemed substantive and we have no other performance obligations related to the milestone and collectability is reasonably assured, which is generally upon receipt, or recognized upon termination of the agreement and all related obligations. Deferred revenue represents amounts received prior to revenue recognition.
 
Revenues from contract research, government grants, and consulting fees are recognized over the respective contract periods as the services are performed, provided there is persuasive evidence or an arrangement, the fee is fixed or determinable and collection of the related receivable is reasonably assured. Once all conditions of the grant are met and no contingencies remain outstanding, the revenue is recognized as grant fee revenue and an earned but unbilled revenue receivable is recorded.
 
Research and Development Expenses
 
Research and development expenses consist of direct and overhead-related research expenses and are expensed as incurred. Costs to acquire technologies, including licenses, that are utilized in research and development and that have no alternative future use are expensed when incurred. Costs of technology developed for use in our products are expensed as incurred until technological feasibility has been established.
 
Clinical Trial Expenses
 
Clinical trial expenses, which are included in research and development expenses, include obligations resulting from our contracts with various clinical research organizations in connection with conducting clinical trials for our product candidates. We recognize expenses for these activities based on a variety of factors, including actual and estimated labor hours, clinical site initiation activities, patient enrollment rates, estimates of external costs and other activity-based factors. We believe that this method best approximates the efforts expended on a clinical trial with the expenses we record. We adjust our rate of clinical expense recognition if actual results differ from our estimates. If our estimates prove incorrect, clinical trial expenses recorded in future periods could vary.
 
 
-14- 

 
Stock-Based Compensation
 
Our stock-based employee compensation plans are described in Note 7 of the Notes to Condensed Financial Statements included in this Quarterly Report. We follow ASC 718, Compensation-Stock Compensation (“ASC 718”), which requires the measurement and recognition of compensation expense for all stock-based awards made to employees.
 
For stock options and warrants paid in consideration of services rendered by non-employees, we recognize compensation expense in accordance with the requirements of ASC 505-50, Equity-Based Payments to Non-Employees (“ASC 505-50”).
 
Non-employee option grants that do not vest immediately upon grant are recorded as an expense over the vesting period. At the end of each financial reporting period prior to performance, the value of these options is determined using the Black-Scholes option-pricing model, and compensation expense recognized or recovered during the period is adjusted accordingly. Since the fair market value of options granted or issued to non-employees is subject to change in the future, the amount of the future compensation expense is subject to adjustment until the common stock options or warrants are fully vested.
 
The fair value of each stock option and warrant is estimated using the Black-Scholes option-pricing model, which uses certain assumptions related to risk-free interest rates, expected volatility, expected life of the stock options and future dividends. Compensation expense is recorded based upon the value derived from the Black-Scholes option-pricing model, based on an expected forfeiture rate that is adjusted for our actual experience. If our Black-Scholes option-pricing model assumptions or our actual or estimated forfeiture rate are different in the future, it could materially affect our compensation expense recorded in future periods.
 
Impairment of Long-Lived Assets
 
We review long-lived assets, including finite-lived intangible assets, for impairment on an annual basis as of December 31, or on an interim basis if an event occurs that might reduce the fair value of such assets below their carrying values. An impairment loss would be recognized based on the difference between the carrying value of the asset and its estimated fair value, which would be determined based on either discounted future cash flows or other appropriate fair value methods. If our estimates used in the determination of either discounted future cash flows or other appropriate fair value methods are not accurate as compared to actual future results, we may be required to record an impairment charge.
 
Net Income (Loss) per Share
 
Basic and diluted net loss per common share is computed using the weighted-average number of common shares outstanding.Potentially dilutive stock options and warrants to purchase 17.8 million shares for each of the three-month and six-month periods ended June 30, 2015, and 14.6 million  shares for each of the three-month and six-month periods ended June 30, 2014, were excluded from the computation of diluted net loss per share, because the effect would be anti-dilutive.
 
Warrant Liabilities
 
Liabilities measured at fair value on a recurring basis include warrant liabilities resulting from our August 2011 equity financing. In accordance with ASC 815-40, Accounting for Derivative Financial Instruments Indexed to and Potentially Settled in a Company’s Own Stock (“ASC 815-40”), the warrant liabilities are recorded at fair value each quarter-end until they are completely settled. The warrants are valued using the Black-Scholes method, using assumptions consistent with our application of ASC 505-50. The gain or loss resulting from the change in fair value is shown on the statements of operations as a gain or loss on warrant derivative liabilities.
 
 
-15- 

 
Liquidity and Capital Resources
 
We have relied primarily upon proceeds from sales of our equity securities and the exercise of options and warrants, and to a much lesser extent upon payments from our strategic partners and licensees, to generate funds needed to finance our business and operations.
 
At June 30, 2015, we had cash and cash equivalents of approximately $38.8 million and short-term investments of approximately $15.0 million.  Management believes that our current cash on hand and short-term investments, along with the $26.8 million of net proceeds received from our underwritten public offering on July 21, 2015, will be sufficient to fund our operations for the foreseeable future.  The estimate is based, in part, upon our currently projected expenditures for the remainder of 2015 and the first six months of 2016 of approximately $53.1 million, which includes approximately $36.1 million for our clinical programs for aldoxorubicin, approximately $2.3 million for pre-clinical development of new albumin-binding cancer drugs, approximately $3.9 million for general operation of our clinical programs, and approximately $10.8 million for other general and administrative expenses (including pre-commercialization). These projected expenditures are also based upon numerous other assumptions and subject to many uncertainties, and our actual expenditures may be significantly different from these projections.
 
If we obtain marketing approval and successfully commercialize aldoxorubicin or other product candidates, we anticipate it will take several years for us to generate significant recurring revenue. We will be dependent on future financing and possible strategic partnerships until such time, if ever, as we can generate significant recurring revenue. We have no commitments from third parties to provide us with any additional financing, and we may not be able to obtain future financing on favorable terms, or at all.  If we fail to obtain sufficient funding when needed, we may be forced to delay, scale back or eliminate all or a portion of our development programs or clinical trials, seek to license to other companies our product candidates or technologies that we would prefer to develop and commercialize ourselves, or seek to sell some or all of our assets or merge with or be acquired by another company.

    We recorded a net loss in the six-months ended June 30, 2015 of $29.2 million as compared to a net loss in the six-months ended June 30, 2014 of $11.1 million, or an increase of $18.1 million.  This was due primarily to an increase in our research and development expenditures in the current six-month period of $5.2 million as compared to comparative 2014 period, resulting from increased expenditures associated with our clinical program for aldoxorubicin, as well as the new expenditures in the 2015 period of $0.8 million associated with our German lab operations.  We also incurred a gain of $0.6 million on warrant derivative liability in the current period, as compared to a gain on warrant derivative liability of $12.2 million in the six-months ended June 30, 2014, for a decrease of $11.6 million.
 
We purchased $18.0 million and sold $48.6 million of short-term investments, for a net decrease of $30.6 million in the six-month period ended June 30, 2015. We purchased $45.6 million and sold $22.1 million of short-term investments, for a net increase of $23.5 million, in the comparable period ended June 30, 2014. We utilized approximately $69,300 for capital expenditures in the six-month period ended June 30, 2015 as compared to approximately $21,000 in the comparable 2014 period. We do not expect any significant capital spending during the next 12 months.
 
We did not conduct any public offering in the six-month period ended June 30, 2015, and we raised net proceeds of $80.5 million from a public offering in the six-month period ended June 30, 2014.
 
We continue to evaluate potential future sources of capital, as we do not currently have commitments from any third parties to provide us with additional capital. The results of our technology licensing efforts and the actual proceeds of any fund-raising activities will determine our ongoing ability to operate as a going concern. Our ability to obtain future financings through joint ventures, product licensing arrangements, royalty sales, equity financings, grants or otherwise is subject to market conditions and our ability to identify parties that are willing and able to enter into such arrangements on terms that are satisfactory to us. Depending upon the outcome of our fundraising efforts, the accompanying financial information may not necessarily be indicative of our future financial condition.
 
As a development company that is primarily engaged in research and development activities, we expect to incur significant losses and negative cash flow from operating activities for the foreseeable future.  There can be no assurance that we will be able to generate revenues from our product candidates and become profitable.  Even if we become profitable, we may not be able to sustain that profitability.
 
 
-16- 

 
Results of Operations
 
We recorded a net loss of approximately $11.7 million and $29.2 million for the three-month and six-month periods ended June 30, 2015, respectively, as compared to a net loss of approximately $15.7 million and $11.1 million for the three-month and six-month periods ended June 30, 2014, respectively. The decrease of $4.0 million in our net loss during the current three-month period resulted primarily from a gain of $2.4 million on warrant derivative liability in the current quarter, as compared to a loss on warrant derivative liability of $2.5 million in the comparative 2014 period, for a difference of $4.9 million.
 
We recognized no licensing revenue in the three or six-month periods ended June 30, 2015 or 2014. All future licensing fees under our current licensing agreements are dependent upon successful development milestones being achieved by the licensor. During the remainder of 2015, we do not anticipate receiving any significant licensing fees.
 
Research and Development
 
   
Three-Month Period Ended
June 30,
   
Six-Month Period Ended
June 30,
 
   
2015
   
2014
   
2015
   
2014
 
   
(In thousands)
   
(In thousands)
 
Research and development expenses
  $ 9,547     $ 10,028     $ 21,707     $ 15,760  
Non-cash research and development expenses
          156             1,227  
Employee stock option expense
    393       235       729       410  
Depreciation and amortization
    68       9       137       19  
    $ 10,008     $ 10,428     $ 22,573     $ 17,416  
                                 

Research expenses are expenses incurred by us in the discovery of new information that will assist us in the creation and the development of new drugs or treatments. Development expenses are expenses incurred by us in our efforts to commercialize the findings generated through our research efforts.  Our research and development expenses, excluding stock option expense, non-cash expenses and depreciation and amortization, were $9.5 million and $21.7 million for the three-month and six-month periods ended June 30, 2015, respectively, and $10.0 million and $15.8 million for the three-month and six-month periods ended June 30, 2014, respectively.
 
Research and development expenses incurred during the three-month period ended June 30, 2015 related primarily to our aldoxorubicin clinical program.  In the three-month and six-month periods ended June 30, 2015, the development expenses of our program for aldoxorubicin were $8.2 million and $19.1 million, respectively, as compared to $9.3 million and $14.2 million for the same periods in 2014, respectively. The 2014 aldoxorubicin program expenses include milestone payments to the licensor of $1.0 million and $2.0 million, respectively, for the three-month and six-month periods ended June 30, 2014, respectively. There were no such milestones paid in 2015. We incurred $0.5 million and $0.9 million, respectively, for the three-month and six-month periods ended June 30, 2015, for our German lab operations, as compared to $0.2 million in the 2014 comparative periods. The remainder of our research and development expenses primarily related to research and development support costs. We recorded no non-cash stock option and warrant expense in the three-month and six-month periods ended June 30, 2015, respectively, as compared to $0.2 million and $1.2 million in the comparative 2014 periods, respectively.  We recorded approximately $0.4 million and $0.7 million of employee stock option expense in the three-month and six-month periods ended June 30, 2015, as compared to $0.2 million and $0.4 million for the same periods in 2014, respectively.
 
 
-17- 

 
General and Administrative Expenses
 
   
Three-Month Period Ended
June 30,
   
Six-Month Period Ended
June 30,
 
   
2015
   
2014
   
2015
   
2014
 
   
(In thousands)
   
(In thousands)
 
General and administrative expenses
  $ 2,298     $ 2,400     $ 4,359     $ 5,004  
Non-cash general and administrative expenses
    141       161       234       353  
Employee stock option expense
    1,744       325       2,700       637  
Depreciation and amortization
    9       23       29       46  
    $ 4,192     $ 2,909     $ 7,322     $ 6,040  

General and administrative expenses include all administrative salaries and general corporate expenses, including legal expenses. Our general and administrative expenses, excluding stock option expense, non-cash expenses and depreciation and amortization, were $2.3million and $4.4 million for the three-month and six-month periods ended June 30, 2015, respectively, and $2.4 million and $5.0 million, respectively, for the same periods in 2014.
 
Employee stock option expense relates to options granted to retain and compensate directors, officers and other employees.  We recorded approximately $1.7 million and $2.7 million of employee stock option expense in the three-month and six-month periods ended June 30, 2015, respectively, as compared $0.3 million and $0.6 million, respectively, for the same periods in 2014. We recorded approximately $0.1 million and $0.2 million of non-employee stock option expense in the three-month and six-month periods, ended June 30, 2015, respectively, and $0.2 million and $0.4 million for the comparative 2014 periods.
 
Depreciation and Amortization
 
Depreciation expense reflects the depreciation of our equipment and furnishings.
 
Interest Income
 
Interest income was approximately $46,000 and $103,000 for the three-month and six-month periods ended June 30, 2015, respectively, as compared to $89,000 and $160,000, respectively, for the same periods in 2014. This decrease was related to the reduction in cash and cash equivalents and short term investments.
 
Item 3. — Quantitative and Qualitative Disclosures About Market Risk
 
Our exposure to market risk is limited primarily to interest income sensitivity, which is affected by changes in the general level of U.S. interest rates, particularly because a significant portion of our investments are in short-term debt securities issued by the U.S. government and institutional money market funds. The primary objective of our investment activities is to preserve principal. Due to the nature of our short-term investments, we believe that we are not subject to any material market risk exposure. We do not have any speculative or hedging derivative financial instruments or foreign currency instruments. If interest rates had varied by 10% in the three-month period ended June 30, 2015, it would not have had a material effect on our results of operations or cash flows for that period.
 
Item 4. Controls and Procedures
 
Evaluation of Disclosure Controls and Procedures
 
Our management, with the participation of our Chief Executive Officer and our Chief Financial Officer, performed an evaluation of the effectiveness of the design and operation of our disclosure controls and procedures (as defined in Securities Exchange Act Rule 13a-15(e)) as of the end of the quarterly period covered by this Quarterly Report. Based on that evaluation, our Chief Executive Officer and our Chief Financial Officer concluded that our disclosure controls and procedures were effective to ensure that information required to be disclosed by us in reports that we file or submit under the Securities Exchange Act of 1934 is recorded, processed, summarized and reported within the time periods specified in the rules and forms of the SEC.
 
Changes in Controls over Financial Reporting
 
There was no change in our internal control over financial reporting that occurred during the quarter ended June 30, 2015 that materially affected, or is reasonably likely to materially affect, our internal control over financial reporting. We continually seek to assure that all of our controls and procedures are adequate and effective. Any failure to implement and maintain improvements in the controls over our financial reporting could cause us to fail to meet our reporting obligations under the SEC’s rules and regulations. Any failure to improve our internal controls to address the weaknesses we have identified could also cause investors to lose confidence in our reported financial information, which could have a negative impact on the trading price of our common stock.
 
 
-18- 

 
PART II — OTHER INFORMATION
 
Item 1A. — Legal Proceedings
 
The disclosure set forth in Note 12 to our financial statements is herein incorporated by reference.
 
We are, and in the future may be, subject to legal or administrative actions that could adversely affect our results of operations and our business.
 
Claims have been threatened and have been brought against the Company and its officers and/or directors. Adverse outcomes with respect to some or all of these claims may result in significant monetary damages or injunctive relief that could adversely affect the Company’s ability to conduct its business. Defending a lawsuit can be expensive and can divert the attention of key employees from operating the Company’s business. Litigation and other claims are subject to inherent uncertainties and management’s view of these matters may change in the future. A material adverse impact on the Company’s financial statements also could occur for the period in which the effect of an unfavorable final outcome becomes probable and reasonably estimable.
 
Item 6. — Exhibits
 
The exhibits listed in the accompanying Index to Exhibits are filed as part of this Quarterly Report and incorporated herein by reference.
 

 

 
-19- 

 

SIGNATURES
 
Pursuant to the requirements of the Securities Exchange Act of 1934, the Registrant has duly caused this report to be signed on its behalf by the undersigned thereunto duly authorized.
 
 
 
CytRx Corporation
 
       
August 3, 2015
By:
/s/ JOHN Y. CALOZ  
    John Y. Caloz  
    Chief Financial Officer  
       
 
 
 
 
-20- 

 

INDEX TO EXHIBITS
 
Exhibit
Number
 
 
Description
31.1    
Certification of Chief Executive Officer Pursuant to 17 CFR 240.13a-14(a)
31.2    
Certification of Chief Financial Officer Pursuant to 17 CFR 240.13a-14(a)
32.1    
Certification of Chief Executive Officer Pursuant to 18 U.S.C. Section 1350, as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002
32.2    
Certification of Chief Financial Officer Pursuant to 18 U.S.C. Section 1350, as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002
101.INS
 
XBRL Instance Document
101.SCH
 
XBRL Schema Document
101.CAL
 
XBRL Calculation Linkbase Document
101.DEF
 
XBRL Definition Linkbase Document
101.LAB
 
XBRL Label Linkbase Document
101.PRE
 
XBRL Presentation Linkbase Document

______________________________

 
-21-
 


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

Exhibit 31.1

CERTIFICATIONS

I, Steven A. Kriegsman, Chief Executive Officer of CytRx Corporation, certify that:
 
1.           I have reviewed this quarterly report on Form 10-Q of CytRx Corporation;
 
2.           Based on my knowledge, this quarterly 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 periods covered by this quarterly report;
 
3.           Based on my knowledge, the financial statements, and other financial information included in this quarterly 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 quarterly 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 subsidiaries, is made known to us by others within those entities, particularly during the period in which this quarterly 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 periods 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.
 
     
       
August 3, 2015
By:
STEVEN A. KRIEGSMAN  
    Steven A. Kriegsman   
    Chief Executive Officer   
       

 
 

 

EX-31.2 3 ex31-2.htm CERTIFICATION OF CHIEF FINANCIAL OFFICER ex31-2.htm
Exhibit 31.2
CERTIFICATIONS
 
I, John Y. Caloz, Chief Financial Officer of CytRx Corporation, certify that:
 
1.           I have reviewed this quarterly report on Form 10-Q of CytRx Corporation;
 
2.           Based on my knowledge, this quarterly 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 periods covered by this quarterly report;
 
3.           Based on my knowledge, the financial statements, and other financial information included in this quarterly 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 quarterly 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  subsidiaries, is made known to us by others within those entities, particularly during the period in which this quarterly 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 periods 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.
 

     
       
August 3, 2015
By:
/s/ JOHN Y. CALOZ  
    John Y. Caloz   
    Chief Financial Officer   
       
 
 
 

 
 

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

Exhibit 32.1

 
Certification of Chief Executive Officer
 
Pursuant to 18 U.S.C. 1350, as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002, the undersigned officer of CytRx Corporation (the “Company”) hereby certifies based on his knowledge that:
 
(i)           the accompanying Quarterly Report on Form 10-Q of the Company for the period ended June 30, 2015 as filed with the Securities and Exchange Commission on the date hereof (the “Report”) fully complies with the requirements of Section 13(a) or Section 15(d), as applicable, of the Securities Exchange Act of 1934, as amended; and
 
(ii)           the information contained in the Report fairly presents, in all material respects, the financial condition and results of operations of the Company as of and for the periods covered in the Report.
 
 
     
       
August 3, 2015
By:
/s/ STEVEN A. KRIEGSMAN  
    Steven A. Kriegsman  
    Chief Executive Officer   
       
 
 
A signed original of this written statement required by Section 906 of the Sarbanes-Oxley Act of 2002 (Section 906), or other document authenticating, acknowledging, or otherwise adopting the signature that appears in typed form within the electronic version of this written statement required by Section 906, has been provided to CytRx Corporation and will be retained by CytRx Corporation and furnished to the Securities and Exchange Commission or its staff upon request.
 
The foregoing certification is being furnished to the Securities and Exchange Commission as an Exhibit to the Form 10-Q and shall not be considered filed as part of the Form 10-Q.
 

 
 

 

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

Exhibit 32.2
 

 
Certification of Chief Financial Officer
 
Pursuant to 18 U.S.C. 1350, as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002, the undersigned officer of CytRx Corporation (the “Company”) hereby certifies based on his knowledge that:
 
(i)           the accompanying Quarterly Report on Form 10-Q of the Company for the period ended June 30, 2015 as filed with the Securities and Exchange Commission on the date hereof (the “Report”) fully complies with the requirements of Section 13(a) or Section 15(d), as applicable, of the Securities Exchange Act of 1934, as amended; and
 
(ii)           the information contained in the Report fairly presents, in all material respects, the financial condition and results of operations of the Company as of and for the periods covered in the Report.
 
 
  Company Name  
       
August 3, 2015
By:
/s/ JOHN Y. CALOZ  
    John Y. Caloz  
    Chief Financial Officer  
       
 
 
A signed original of this written statement required by Section 906 of the Sarbanes-Oxley Act of 2002 (Section 906), or other document authenticating, acknowledging, or otherwise adopting the signature that appears in typed form within the electronic version of this written statement required by Section 906, has been provided to CytRx Corporation and will be retained by CytRx Corporation and furnished to the Securities and Exchange Commission or its staff upon request.
 
The foregoing certification is being furnished to the Securities and Exchange Commission as an Exhibit to the Form 10-Q and shall not be considered filed as part of the Form 10-Q.
 

 

 




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The Company is currently focused on the clinical development of aldoxorubicin (formerly known as INNO-206), its modified version of the widely-used chemotherapeutic agent, doxorubicin. CytRx previously reported positive top-line efficacy results (median progression-free survival, or PFS, PFS at six months, overall response rates, hazard ratios and overall survival) from its completed, global Phase 2b clinical trial with aldoxorubicin as a treatment for soft tissue sarcoma, or STS. Hazard ratios, or the likelihood that the study endpoint (in this case tumor progression) will be reached during a given period, are an important measure of the reliability and uniformity of the absolute data for PFS. The trial investigated the efficacy and safety of aldoxorubicin compared with doxorubicin in subjects with first-line metastatic, locally advanced or unresectable STS. Aldoxorubicin combines the chemotherapeutic agent doxorubicin with a novel linker-molecule that binds specifically to albumin in the blood and is designed to allow for delivery of higher amounts of doxorubicin (3&#189; to 4 times) without the major dose-limiting toxicities as seen with the administration of doxorubicin alone.</div><div style="text-align: justify; margin-left: 0pt; display: block; margin-right: 0pt; text-indent: 0pt;">&#160;</div><div style="font-size: 10pt; font-family: Times New Roman; text-align: left; margin-left: 0pt; display: block; margin-right: 0pt; text-indent: 36pt;">In the first quarter of 2014, the Company initiated a pivotal Phase 3 trial of aldoxorubicin as a therapy for patients with STS whose tumors have progressed following treatment with chemotherapy. The Phase 3 trial is being conducted under a Special Protocol Assessment, or SPA, granted by the FDA. The SPA means that the FDA agrees that the design and analyses proposed in the Phase 3 trial protocol are acceptable to support regulatory approval of the product candidate with respect to effectiveness of the indication studied, and will not change its perspective on these matters, except in limited circumstances such as where a sponsor fails to follow a protocol agreed to with the FDA or where previously unrecognized health concerns occur.&#160;&#160;Thus, if the study demonstrates an acceptable benefit-risk profile as determined by the FDA, it will support registration of aldoxorubicin for this indication.&#160;&#160;If approved for marketing, the Company&#8217;s current plan would be to commercially launch aldoxorubicin in late 2017.</div><div style="text-align: justify; margin-left: 0pt; display: block; margin-right: 0pt; text-indent: 0pt;">&#160;</div><div style="font-size: 10pt; font-family: Times New Roman; text-align: left; margin-left: 0pt; display: block; margin-right: 0pt; text-indent: 36pt;">CytRx is currently evaluating aldoxorubicin in a global Phase 2b clinical trial in small cell lung cancer, a Phase 2 clinical trial in HIV-related Kaposi's sarcoma, a Phase 2 clinical trial in patients with late-stage glioblastoma (brain cancer), a Phase 1b clinical trial in combination with ifosfamide in patients with STS and a Phase 1b clinical trial in combination with gemcitabine in patients with metastatic solid tumors. The Company has completed a global Phase 2b clinical trial with aldoxorubicin as a 1st-line therapy for STS, a Phase 1b/2 clinical trial primarily in the same indication, a Phase 1b clinical trial of aldoxorubicin in combination with doxorubicin in patients with advanced solid tumors and a Phase 1b pharmacokinetics clinical trial in patients with metastatic solid tumors.</div><div style="text-align: justify; margin-left: 0pt; display: block; margin-right: 0pt; text-indent: 0pt;">&#160;</div><div style="font-size: 10pt; font-family: Times New Roman; text-align: left; margin-left: 0pt; display: block; margin-right: 0pt; text-indent: 36pt;">CytRx plans to expand its pipeline of oncology candidates through its drug-development activities at its laboratory facility in Freiburg, Germany, based on its Linker Activated Drug Release, or LADR&#8482;, technology that can be utilized with multiple chemotherapeutic agents and may allow for greater drug concentration at tumor sites.</div><div style="text-align: justify; margin-left: 0pt; display: block; margin-right: 0pt; text-indent: 0pt;">&#160;</div><div style="font-size: 10pt; font-family: Times New Roman; text-align: left; margin-left: 0pt; display: block; margin-right: 0pt; text-indent: 36pt;">The accompanying condensed financial statements at June 30, 2015 and for the three-month and six-month periods ended June 30, 2015 and 2014, respectively, are unaudited, but include all adjustments, consisting of normal recurring entries, that management believes to be necessary for a fair presentation of the periods presented. 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On October 1, 2014, plaintiffs filed a consolidated amended complaint on behalf of all persons who purchased or otherwise acquired the publicly traded securities of CytRx between November 20, 2013 and March 13, 2014, against CytRx, certain Company officers and directors, a freelance writer, and certain underwriters. The complaint alleges that certain of the defendants violated the Securities Exchange Act of 1934 by making materially false and misleading statements in press releases, promotional articles, SEC filings and other public statements. The complaint further alleges that certain of the defendants violated the Securities Act of 1933 by making materially misleading statements and omitting material information in the shelf Registration Statement on Form S-3 filed with the SEC on December 6, 2012 and Prospectus Supplement on Form 424(b)(2) filed with the SEC on January 31, 2014. 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border-bottom: black 2px solid; text-align: right;">6,165,528</td><td nowrap="nowrap" valign="bottom" style="font-size: 10pt; font-family: times new roman; width: 1%; padding-bottom: 2px; text-align: left;">&#160;</td></tr><tr bgcolor="white"><td align="left" valign="bottom" style="width: 64%; padding-bottom: 4px;"><div style="font-size: 10pt; font-family: times new roman; text-align: left; margin-left: 9pt; display: block; margin-right: 5.05pt; text-indent: 0pt;"><font style="letter-spacing: 9pt;">&#160;&#160;&#160;</font>&#160;Total current assets</div></td><td align="left" valign="bottom" style="font-size: 10pt; font-family: times new roman; width: 1%; padding-bottom: 4px;">&#160;</td><td valign="bottom" style="font-size: 10pt; font-family: times new roman; width: 1%; border-bottom: black 4px double; text-align: left;">&#160;</td><td valign="bottom" style="font-size: 10pt; font-family: times new roman; width: 9%; border-bottom: black 4px double; text-align: right;">60,001,477</td><td nowrap="nowrap" valign="bottom" style="font-size: 10pt; 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font-family: times new roman; width: 1%; padding-bottom: 2px; text-align: left;">&#160;</td><td align="left" valign="bottom" style="font-size: 10pt; font-family: times new roman; width: 1%; padding-bottom: 2px;">&#160;</td><td valign="bottom" style="font-size: 10pt; font-family: times new roman; width: 1%; border-bottom: black 2px solid; text-align: left;">&#160;</td><td valign="bottom" style="font-size: 10pt; font-family: times new roman; width: 9%; border-bottom: black 2px solid; text-align: right;">&#8212;</td><td nowrap="nowrap" valign="bottom" style="font-size: 10pt; font-family: times new roman; width: 1%; padding-bottom: 2px; text-align: left;">&#160;</td><td align="left" valign="bottom" style="font-size: 10pt; font-family: times new roman; width: 1%; padding-bottom: 2px;">&#160;</td><td valign="bottom" style="font-size: 10pt; font-family: times new roman; width: 1%; border-bottom: black 2px solid; text-align: left;">&#160;</td><td valign="bottom" style="font-size: 10pt; font-family: times new roman; 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font-family: times new roman; width: 1%; display: inline;">&#160;</td><td valign="bottom" style="font-size: 10pt; font-family: times new roman; width: 1%; text-align: left;">&#160;</td><td valign="bottom" style="font-size: 10pt; font-family: times new roman; width: 9%; text-align: right;">&#160;</td><td nowrap="nowrap" valign="bottom" style="font-size: 10pt; font-family: times new roman; width: 1%; text-align: left;">&#160;</td></tr><tr bgcolor="#cceeff"><td valign="bottom" style="font-size: 10pt; font-family: times new roman; width: 64%; display: inline;">&#160; </td><td valign="bottom" style="font-size: 10pt; font-family: times new roman; width: 1%; display: inline;">&#160;</td><td valign="bottom" style="font-size: 10pt; font-family: times new roman; width: 1%; text-align: left;">&#160;</td><td valign="bottom" style="font-size: 10pt; font-family: times new roman; width: 9%; text-align: right;">&#160;</td><td nowrap="nowrap" valign="bottom" style="font-size: 10pt; font-family: times new roman; 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style="font-size: 10pt; font-family: times new roman; text-align: left; margin-left: 0pt; display: block; margin-right: 0pt; text-indent: 0pt;">Current assets:</div></td><td valign="bottom" style="font-size: 10pt; font-family: times new roman; display: inline;">&#160;</td><td colspan="2" valign="bottom" style="font-size: 10pt; font-family: times new roman; display: inline;">&#160;</td><td nowrap="nowrap" valign="bottom" style="font-size: 10pt; font-family: times new roman; text-align: left;">&#160;</td><td valign="bottom" style="font-size: 10pt; font-family: times new roman; display: inline;">&#160;</td><td colspan="2" valign="bottom" style="font-size: 10pt; font-family: times new roman; display: inline;">&#160;</td><td nowrap="nowrap" valign="bottom" style="font-size: 10pt; font-family: times new roman; text-align: left;">&#160;</td><td valign="bottom" style="font-size: 10pt; font-family: times new roman; display: inline;">&#160;</td><td colspan="2" valign="bottom" style="font-size: 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style="font-size: 10pt; font-family: times new roman; width: 1%; padding-bottom: 2px;">&#160;</td><td valign="bottom" style="font-size: 10pt; font-family: times new roman; width: 1%; border-bottom: black 2px solid; text-align: left;">&#160;</td><td valign="bottom" style="font-size: 10pt; font-family: times new roman; width: 9%; border-bottom: black 2px solid; text-align: right;">6,165,528</td><td nowrap="nowrap" valign="bottom" style="font-size: 10pt; font-family: times new roman; width: 1%; padding-bottom: 2px; text-align: left;">&#160;</td><td align="left" valign="bottom" style="font-size: 10pt; font-family: times new roman; width: 1%; padding-bottom: 2px;">&#160;</td><td valign="bottom" style="font-size: 10pt; font-family: times new roman; width: 1%; border-bottom: black 2px solid; text-align: left;">&#160;</td><td valign="bottom" style="font-size: 10pt; font-family: times new roman; width: 9%; border-bottom: black 2px solid; text-align: right;">&#8212;</td><td nowrap="nowrap" 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style="font-size: 10pt; font-family: times new roman; width: 1%; text-align: left;">&#160;</td><td valign="bottom" style="font-size: 10pt; font-family: times new roman; width: 1%; display: inline;">&#160;</td><td valign="bottom" style="font-size: 10pt; font-family: times new roman; width: 1%; text-align: left;">&#160;</td><td valign="bottom" style="font-size: 10pt; font-family: times new roman; width: 9%; text-align: right;">&#160;</td><td nowrap="nowrap" valign="bottom" style="font-size: 10pt; font-family: times new roman; width: 1%; text-align: left;">&#160;</td></tr><tr bgcolor="white"><td align="left" valign="bottom" style="width: 64%;"><div style="font-size: 10pt; font-family: times new roman; font-weight: bold; display: block; text-indent: 0pt;">LIABILITIES AND STOCKHOLDERS&#8217; EQUITY</div></td><td valign="bottom" style="font-size: 10pt; font-family: times new roman; width: 1%; display: inline;">&#160;</td><td valign="bottom" style="font-size: 10pt; font-family: times new 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left;">&#160;</td><td valign="bottom" style="font-size: 10pt; font-family: times new roman; width: 9%; text-align: right;">&#160;</td><td nowrap="nowrap" valign="bottom" style="font-size: 10pt; font-family: times new roman; width: 1%; text-align: left;">&#160;</td></tr><tr bgcolor="#cceeff"><td valign="bottom" style="font-size: 10pt; font-family: times new roman; width: 64%; display: inline;">&#160; </td><td valign="bottom" style="font-size: 10pt; font-family: times new roman; width: 1%; display: inline;">&#160;</td><td valign="bottom" style="font-size: 10pt; font-family: times new roman; width: 1%; text-align: left;">&#160;</td><td valign="bottom" style="font-size: 10pt; font-family: times new roman; width: 9%; text-align: right;">&#160;</td><td nowrap="nowrap" valign="bottom" style="font-size: 10pt; font-family: times new roman; width: 1%; text-align: left;">&#160;</td><td valign="bottom" style="font-size: 10pt; font-family: times new roman; width: 1%; display: 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nowrap="nowrap" valign="bottom" style="font-size: 10pt; font-family: times new roman; width: 1%; padding-bottom: 4px; text-align: left;">&#160;</td><td align="left" valign="bottom" style="font-size: 10pt; font-family: times new roman; width: 1%; padding-bottom: 4px;">&#160;</td><td valign="bottom" style="font-size: 10pt; font-family: times new roman; width: 1%; padding-bottom: 4px; text-align: left;">&#160;</td><td valign="bottom" style="font-size: 10pt; font-family: times new roman; width: 9%; padding-bottom: 4px; text-align: right;">&#160;</td><td nowrap="nowrap" valign="bottom" style="font-size: 10pt; font-family: times new roman; width: 1%; padding-bottom: 4px; text-align: left;">&#160;</td></tr><tr bgcolor="#cceeff"><td align="left" valign="bottom" style="font-size: 10pt; font-family: times new roman; width: 64%; padding-bottom: 4px; padding-left: 0pt; margin-left: 9pt;">&#160;&#160;&#160;&#160; Accounts payable and other current liabilities&#160;<font style="letter-spacing: 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and liabilities measured at fair value on a recurring basis [Abstract] Level III [Member] Level I [Member] Level II [Member] Foreign Currency Remeasurement Net foreign exchange loss Foreign Currency Transaction Gain (Loss), Unrealized Foreign Currency Remeasurement [Abstract] General and administrative General and Administrative Expense [Member] Goodwill Schedule of employee and non employee share based compensation allocation of recognized period costs by report line [Axis] CONDENSED STATEMENTS OF OPERATIONS (Unaudited) [Abstract] Income Taxes [Abstract] Income Tax Authority [Axis] Employee and non employee share based compensation allocation of recognized period costs report line [Domain] Income Tax Authority [Domain] Income Taxes Income Tax Disclosure [Text Block] Cash paid for income taxes Receivables Increase (Decrease) in Accounts Receivable Accounts payable Accrued expenses and other current liabilities Interest receivable Increase (Decrease) in Accrued Interest Receivable, Net Changes in assets and liabilities: Prepaid expenses and other current assets Increase (Decrease) in Prepaid Expense and Other Assets Interest receivable Interest income Short-term Investments Investments in Debt and Marketable Equity Securities (and Certain Trading Assets) Disclosure [Text Block] IPO [Member] Total current liabilities Total current liabilities Current liabilities: LIABILITIES AND STOCKHOLDERS' EQUITY Total liabilities and stockholders' equity Liabilities and Equity License revenue Licenses Revenue Fees and expenses related to settlement Litigation Settlement, Expense Estimated projected expenditure type [Domain] Estimated projected expenditures [Axis] Number of shareholders lawsuits Major Types of Debt and Equity Securities [Domain] Schedule of Available-for-sale Securities, Major Types of Debt and Equity Securities [Axis] Short-term Investments [Abstract] Maximum [Member] Minimum [Member] Cash flows from financing activities: Cash flows from operating activities: Net cash provided by (used in) investing activities Net Cash Provided by (Used in) Investing Activities, Continuing Operations Net cash used in operating activities Net Cash Provided by (Used in) Operating Activities, Continuing Operations Net loss Net loss Net Income (Loss) Attributable to Parent Cash flows from investing activities: Net cash provided by financing activities Net Cash Provided by (Used in) Financing Activities, Continuing Operations Other income (loss): Nonoperating Income (Expense) [Abstract] Underwriters Option [Member] Expenses: Loss before other income (loss) Operating Income (Loss) Operating Loss Carryforwards [Table] Operating Loss Carryforwards [Line Items] Operating loss carryforwards, expiration date Operating Loss Carryforwards, Expiration Date Operating loss carryforwards Operating Loss Carryforwards (Gain) loss on foreign currency translation adjustment Other assets Other income (loss), net Proceeds from the sale of short-term investments Payments for (Proceeds from) Short-term Investments Purchase of short-term investments Payments to Acquire Investments Purchases of equipment and furnishings Payments to Acquire Property, Plant, and Equipment Plan Name [Axis] Plan Name [Domain] Potential future payments Preferred Stock, par value (in dollars per share) Preferred Stock, $0.01 par value, 5,000,000 shares authorized, including 25,000 shares of Series A Junior Participating Preferred Stock; no shares issued and outstanding Preferred Stock, shares issued (in shares) Preferred Stock, shares authorized (in shares) Preferred Stock, shares outstanding (in shares) Prepaid expenses and other current assets Prepaid and other current assets Pro Forma [Member] Pro Forma [Member] Net proceeds from exercise of warrants and stock options Proceeds from issuance of restricted stock to employee Proceeds from the issuance of warrants Net proceeds from public offering Proceeds, exclusive of treasury shares Net proceeds received from underwritten public offering Net proceeds from issuance of common stock Equipment and furnishings, net Range [Domain] Range [Axis] Receivables Outstanding Receivable Research and development Research and Development Expense [Member] Restricted Stock [Member] Accumulated deficit Weighted-Average Remaining Contractual Life Share-based Compensation, Shares Authorized under Stock Option Plans, Exercise Price Range, Exercisable Options, Weighted Average Remaining Contractual Term Weighted-Average Exercise Price, Options Exercisable (in dollars per share) Expected lives Weighted-Average Remaining Contractual Life Weighted-Average Exercise Price (in dollars per share) Sale of Stock [Domain] Revenue: Adjustment [Member] Actual [Member] Scenario, Unspecified [Domain] Fair value measurements by level for assets and liabilities measured at fair value on a recurring basis Schedule of Fair Value, Assets and Liabilities Measured on Recurring Basis [Table Text Block] Schedule of share-based compensation, stock options, activity Schedule of share-based payment award, fair value of the stock options granted , assumptions Schedule of Available-for-sale Securities [Table] Schedule of Available-for-sale Securities [Line Items] Schedule of Share-based Compensation, Shares Authorized under Stock Option Plans, by Exercise Price Range [Table] Schedule of Share-based Compensation Arrangements by Share-based Payment Award [Table] Schedule of share-based compensation, summarizes significant ranges of outstanding stock options Restricted stock granted (in shares) Exercise price (in dollars per share) Share-based Compensation Arrangements by Share-based Payment Award, Options, Exercises in Period, Weighted Average Exercise Price Stock-based compensation expense Restricted shares granted (in shares) Expiration date Share-based Compensation Arrangement by Share-based Payment Award, Expiration Date Weighted-Average Exercise Price Options [Abstract] Share-based Compensation Arrangement by Share-based Payment Award, Options, Outstanding, Weighted Average Exercise Price [Abstract] Share-based Compensation Arrangement by Share-based Payment Award [Line Items] Warrants outstanding (in shares) Share-based Compensation Arrangement by Share-based Payment Award, Non-Option Equity Instruments, Outstanding, Number Common stock per share value (in dollars per share) Share price (in dollars per share) Closing price of the common stock (in dollars per share) Granted (in dollars per share) Granted (in shares) Options exercisable at end of period (in dollars per share) Share-based Compensation Arrangement by Share-based Payment Award, Options, Exercisable, Weighted Average Exercise Price Share-based Compensation Arrangement by Share-based Payment Award, Fair Value Assumptions, Method Used Expected dividend yield (in hundredths) Share-based Compensation Arrangement by Share-based Payment Award, Fair Value Assumptions, Expected Dividend Rate Options exercisable at end of period (in shares) Share-based Compensation Arrangement by Share-based Payment Award, Options, Exercisable, Number Share-based compensation, shares available for future grant (in shares) Expected volatility (in hundredths) Expected volatility (in hundredths) Risk-free interest rate (in hundredths) Share-based Compensation Arrangement by Share-based Payment Award, Fair Value Assumptions, Risk Free Interest Rate Share-based compensation arrangement by share-based payment award, fair value assumptions and methodology [Abstract] Share-based Compensation, Shares Authorized under Stock Option Plans, by Exercise Price Range [Axis] The aggregate intrinsic value of outstanding options Equity Award [Domain] Share-based compensation arrangement by share-based payment award, shares issued in period (in shares) Share-based Compensation, Shares Authorized under Stock Option Plans, Exercise Price Range [Line Items] Outstanding at end of period (in shares) Outstanding at beginning of period (in shares) Share-based Compensation Arrangement by Share-based Payment Award, Options, Outstanding, Number Outstanding at end of period (in dollars per share) Outstanding at beginning of period (in dollars per share) Share-based Compensation Arrangement by Share-based Payment Award, Options, Outstanding, Weighted Average Exercise Price Total stock-based compensation expense resulting from stock options and warrants [Abstract] Share-based Compensation, Shares Authorized under Stock Option Plans, Exercise Price Range [Domain] Number of Options (Employees and Non-Employees) [Abstract] Share-based Compensation Arrangement by Share-based Payment Award, Options, Outstanding [Roll Forward] Total Number of Options (in shares) Total Number of Options Exercisable (in shares) Range of Exercise Prices, Upper Range (in dollars per share) Range of Exercise Prices, Lower Range (in dollars per share) State [Member] CONDENSED STATEMENTS OF CASH FLOWS (Unaudited) [Abstract] Scenario [Axis] CONDENSED BALANCE SHEETS (Unaudited) [Abstract] Common shares issued from the exercise of warrants (in shares) Stock issued, underwritten public offering, value Stock issued, underwritten public offering, value Stock issued, underwritten public offering, value (in shares) Stock issued underwritten public offering (in shares) Equity Transactions Stockholders' Equity Note Disclosure [Text Block] Stockholders' equity Equity Transactions [Abstract] Total stockholders' equity Stockholders' Equity Attributable to Parent Subsequent Event Type [Axis] Subsequent Event [Line Items] Subsequent Event [Member] Subsequent Events Subsequent Events [Abstract] Subsequent Event Type [Domain] Subsequent Event [Table] Sale of Stock [Axis] Supplemental disclosure of cash flow information: Employee and non employee share based compensation by report line [Domain] Schedule of employee and non employee share based compensation by report line [Axis] Treasury stock (in shares) Treasury stock, at cost (199,275 shares) Treasury stock Treasury Stock, Value Unrealized gain recognized Warrants [Member] Basic and diluted weighted-average shares outstanding (in shares) Weighted Average Number of Shares Outstanding, Basic and Diluted Liquidity and Capital Resources [Abstract] The entire disclosure for liquidity and capital resources. Liquidity and Capital Resources [Text Block] Liquidity and Capital Resources This line item represents the amount of operating loss carryforwards available to reduce future taxable income, on which there are no limitations on its use. Operating loss carryforwards unrestricted Operating loss carryforwards, unrestricted Warrant Liabilities [Abstract] The entire disclosure of warrants or rights issued, specifically related to equity financing, and the accounting treatment of gain or loss prior to final settlement. Warrant Liabilities [Text Block] Warrant Liabilities Tabular disclosure of the significant assumptions, including, but not limited to: (a) expected term of share options and similar instruments, (b) expected volatility of the entity's shares, (c) expected dividends, (d) risk-free rate(s), and (e) discount for post-vesting restrictions. Schedule of weighted average assumptions [Table Text Block] Schedule of weighted-average assumptions Schedule that describes that estimated projected expenditure by an entity. Estimated projected expenditures [Table] Line items represent the estimated projected expenditure. Estimated projected expenditure [Line Items] Monetary value refers to the entity estimate currently projected expenditures. Currently projected expenditures for clinical programs Refers to currently projected expenditures for clinical programs for general operation. General operation [Member] General Operation [Member] Refers to currently projected expenditures for clinical programs for aldoxorubicin. Aldoxorubicin [Member] Refers to currently projected expenditures for clinical programs for other programs. Other Programs [Member] Refers to currently projected expenditures for clinical programs for other general and administrative expenses. Other general and administrative expenses [Member] Other General and Administrative Expenses [Member] The non-cash expense recorded for the issuance of restricted stock. Shares issued, non-cash expense Non-cash expense of shares issued Tabular disclosure of selected pro forma balance sheet data giving retroactive effect to the completion of the underwritten offering. Schedule Of Selected Pro Forma Balance Sheet Data [Table Text Block] Schedule of selected pro forma balance sheet data The cash flow associated with cashless warrant exercises. Cashless warrant exercises Incremental common shares attributable to stock options and warrants. A contract that gives the holder the right, but not the obligation, either to purchase or to sell a certain number of shares of stock at a predetermined price for a specified period of time. Stock Options And Warrants [Member] Value of restricted share issued. Value of Restricted Shares Issued Value of restricted shares issued The estimated an annualized forfeiture rate for options granted to employees. Estimated annualized forfeiture rate Estimated annualized forfeiture rate (in hundredths) Share based compensation stock options activity [Abstract] Contractual term of share-based compensation awards, in 'PnYnMnDTnHnMnS' format, for example, 'P1Y5M13D' represents the reported fact of one year, five months, and thirteen days. Share Based Compensation Arrangement By Share Based Payment Award Contractual Term Contractual term Refers to share-based compensation arrangements by share-based payment award, options, exercised, forfeitures, expired in period, weighted average exercise price. Share-based Compensation Arrangements by Share-based Payment Award, Options, Exercised, Forfeitures, Expired in Period, Weighted Average Exercise Price Expired A person serving on the board of directors (who collectively have responsibility for determining the overall policy of the entity and appointing officers) generally elected by the shareholders and an arrangement whereby an non employee stock-based compensation expense is classified. Directors and nonemployees [Member] An arrangement whereby an non-employees stock-based compensation expense is classified. Non employees [Member] Non-Employees [Member] Persons who are responsible for achieving the objectives of the entity and who have the authority to establish policies and make decisions by which those objectives are to be pursued. Senior management [Member] An arrangement whereby an employees stock-based compensation expense is classified. Employees [Member] A person serving on the board of directors (who collectively have responsibility for determining the overall policy of the entity and appointing officers) generally elected by the shareholders and an arrangement whereby an employee stock-based compensation expense is classified. Employees and Directors [Member] The 2000 Long-term incentive plan, reward system designed to improve employees' long term performance by providing rewards. 2000 Long Term Incentive Plan [Member] The 2008 stock incentive plan, reward system designed to improve employees' performance by providing rewards. 2008 Stock Incentive Plan [Member] Schedule that sets forth the allocation of equity-based compensation costs ,this may include the reporting line for the costs and the amount capitalized and expensed of employee and non employee. Schedule of employee and non employee service share based compensation allocation of recognized period costs [Table] Line items represent financial concepts included in a table. These concepts are used to disclose reportable information associated with domain members defined in one or many axes to the table of allocation of recognized period costs of employee and non employee. Employee and non employee share based compensation allocation of recognized period costs by report [Line Items] Intrinsic value of options vested. Excludes equity instruments other than options, for example, but not limited to, share units, stock appreciation rights, restricted stock. Share based Compensation Arrangement by Share based Payment Award, Options, Vested in Period, Intrinsic Value Aggregate intrinsic value of options vested Weighted-average price of equity instruments other than options outstanding, including both vested and non-vested instruments. Share Based Compensation Arrangement By Share Based Payment Award Non Option Equity Instruments Outstanding weighted average price Weighted-average exercise price of warrants outstanding (in dollars per share) Share based compensation, shares authorized under significant ranges of outstanding stock option plans in period [Abstract] Type of estimate of range of exercise prices, one including, but not limited to, upper and lower bound amounts, maximum and minimum amounts, and point estimates. Range Three [Member] Range $ 3.51 - 8.00 [Member] Type of estimate of range of exercise prices, one including, but not limited to, upper and lower bound amounts, maximum and minimum amounts, and point estimates. Range Two [Member] Range $ 2.51 - 3.50 [Member] Type of estimate of range of exercise prices, one including, but not limited to, upper and lower bound amounts, maximum and minimum amounts, and point estimates. Range Four [Member] Range $ 8.01 - 32.55 [Member] Type of estimate of range of exercise prices, one including, but not limited to, upper and lower bound amounts, maximum and minimum amounts, and point estimates. Range One [Member] Range $ 1.83 - 2.50 [Member] Refers to share-based compensation arrangements by share-based payment award, options, exercised, forfeitures, expired in period. Share-based Compensation Arrangements by Share-based Payment Award, Options, Exercised, Forfeitures, Expired in Period Expired (in shares) Description of Company and Basis of Presentation [Abstract] Recent Accounting Pronouncements [Abstract] The entire disclosure of financial statement line items and the effect of the guidance on the financial statement line items if the entity elects recent accounting pronouncements. Recent Accounting Pronouncements [Text Block] Recent Accounting Pronouncements The maximum number of participating junior series preferred shares (or preferred stock redeemable solely at the option of the issuer) permitted to be issued by an entity's charter and bylaws. Series A Junior Participating Preferred Stock, shares authorized Series A Junior Participating Preferred Stock, shares authorized (in shares) Tabular disclosure of total share-based compensation expense resulting from stock options and warrants included in the company's unaudited interim statements of operations. Schedule of total stock based compensation expense from stock options and warrants [Table Text Block] Schedule of total stock-based compensation expense from stock options and warrants Represents the number of programs in clinical development for cancer indications. Number of programs in clinical development for cancer indications Document and Entity Information [Abstract] Fair value portion of a security that gives the holder the right to purchase shares of stock in accordance with the terms of the instrument, usually upon payment of a specified amount. Warrant Liability, Fair Value Disclosure Warrant liabilities This element represents the portion of the balance sheet assertion valued at fair value by the entity whether such amount is presented as a separate caption or as a parenthetical disclosure. Additionally, this element may be used in connection with the fair value disclosures required in the footnote disclosures to the financial statements. Investments which are intended to be sold in the short term (usually less than one year or the normal operating cycle, whichever is longer) including trading securities, available-for-sale securities, held-to-maturity securities, and other short-term investments not otherwise listed in the existing taxonomy. Short Term Investments Fair Value Short-term investments Refers to number of days court afforded the plaintiffs to amend their complaint. Number of Days the Court Gave the Plaintiff to File an Amended Complaint Number of day's court afforded the plaintiffs to amend their complaint The payments made during the period on achievement of clinical milestones. Payments made on achievement of clinical milestones The potential future milestone payments on each additional final marketing approval as of the balance sheet date. Potential future milestone payments on each additional final marketing approval The number of clinical milestones. 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Commitments and contingencies (Details)
6 Months Ended
Jun. 02, 2015
USD ($)
$ / shares
Dec. 10, 2013
$ / shares
Jun. 30, 2015
USD ($)
ClinicalMilestone
d
Lawsuit
Dec. 31, 2014
USD ($)
Commitments and contingencies [Abstract]        
Potential future payments     $ 7,500,000  
Number of clinical milestones | ClinicalMilestone     2  
Number of day's court afforded the plaintiffs to amend their complaint | d     30  
Payments made on achievement of clinical milestones     $ 2,000,000  
Potential future milestone payments on each additional final marketing approval     $ 1,000,000  
Number of shareholders lawsuits | Lawsuit     3  
Exercise price (in dollars per share) | $ / shares $ 4.66 $ 2.39    
Fees and expenses related to settlement $ 1,100,000      
Outstanding Receivable     $ 5,175,007 $ 2,019,293
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Short-term Investments (Details) - USD ($)
6 Months Ended
Jun. 30, 2015
Dec. 31, 2014
Schedule of Available-for-sale Securities [Line Items]    
Short-term investments $ 15,002,213 $ 45,621,593
Certificates of Deposit [Member]    
Schedule of Available-for-sale Securities [Line Items]    
Maturity date of investments Aug. 27, 2015  
XML 16 R9.htm IDEA: XBRL DOCUMENT v3.2.0.727
Short-term Investments
6 Months Ended
Jun. 30, 2015
Short-term Investments [Abstract]  
Short-term Investments
4.           Short-term Investments
 
The Company held $15.0 million of short-term investments at June 30, 2015, as compared to $45.6 million at December 31, 2014.  The Company has classified these investments as available for sale.  These investments are federally insured certificates of deposit with a maturity date of August 27, 2015.
XML 17 R29.htm IDEA: XBRL DOCUMENT v3.2.0.727
Fair Value Measurements (Details) - Recurring [Member] - USD ($)
$ in Thousands
6 Months Ended
Jun. 30, 2015
Dec. 31, 2014
Fair value measurements by level for assets and liabilities measured at fair value on a recurring basis [Abstract]    
Cash equivalents $ 38,437 $ 31,159
Short-term investments 15,002 45,622
Warrant liabilities (4,567) (5,131)
Level I [Member]    
Fair value measurements by level for assets and liabilities measured at fair value on a recurring basis [Abstract]    
Cash equivalents 38,437 31,159
Short-term investments 15,002 45,622
Warrant liabilities 0 0
Level II [Member]    
Fair value measurements by level for assets and liabilities measured at fair value on a recurring basis [Abstract]    
Cash equivalents 0 0
Short-term investments 0 0
Warrant liabilities 0 0
Level III [Member]    
Fair value measurements by level for assets and liabilities measured at fair value on a recurring basis [Abstract]    
Cash equivalents 0 0
Short-term investments 0 0
Warrant liabilities (4,567) $ (5,131)
Unrealized gain recognized $ 600  
XML 18 R28.htm IDEA: XBRL DOCUMENT v3.2.0.727
Stock Based Compensation (Details)
3 Months Ended 6 Months Ended
Jun. 30, 2015
USD ($)
$ / shares
shares
Jun. 30, 2014
USD ($)
$ / shares
Jun. 30, 2015
USD ($)
$ / shares
shares
Jun. 30, 2014
USD ($)
$ / shares
shares
Dec. 31, 2014
$ / shares
shares
Feb. 05, 2014
$ / shares
Share based compensation, shares authorized under significant ranges of outstanding stock option plans in period [Abstract]            
Closing price of the common stock (in dollars per share) | $ / shares           $ 6.50
Employees [Member]            
Share-based compensation arrangement by share-based payment award, fair value assumptions and methodology [Abstract]            
Estimated annualized forfeiture rate (in hundredths)     10.00% 12.00%    
Employees and Directors [Member]            
Share-based compensation arrangement by share-based payment award, fair value assumptions and methodology [Abstract]            
Unrecognized compensation expense related to unvested stock options, granted | $ $ 4,900,000   $ 4,900,000      
Unrecognized compensation cost, recognized as expense over a weighted-average period     1 year 11 days      
Senior management [Member]            
Share-based compensation arrangement by share-based payment award, fair value assumptions and methodology [Abstract]            
Estimated annualized forfeiture rate (in hundredths)     2.00% 2.00%    
Directors and nonemployees [Member]            
Share-based compensation arrangement by share-based payment award, fair value assumptions and methodology [Abstract]            
Estimated annualized forfeiture rate (in hundredths)     0.00% 0.00%    
Stock Options [Member]            
Share-based compensation arrangement by share-based payment award, fair value assumptions and methodology [Abstract]            
Share-based Compensation Arrangement by Share-based Payment Award, Fair Value Assumptions, Method Used     Black-Scholes option-pricing model      
Contractual term     10 years      
Number of Options (Employees and Non-Employees) [Abstract]            
Outstanding at beginning of period (in shares)     10,040,735      
Granted (in shares)     550,000 300,000    
Expired (in shares)     (124,429)      
Outstanding at end of period (in shares) 10,466,306   10,466,306      
Options exercisable at end of period (in shares) 6,911,989   6,911,989      
Weighted-Average Exercise Price Options [Abstract]            
Outstanding at beginning of period (in dollars per share) | $ / shares     $ 2.87      
Granted (in dollars per share) | $ / shares     3.86      
Expired | $ / shares     6.90      
Outstanding at end of period (in dollars per share) | $ / shares $ 3.33   3.33      
Options exercisable at end of period (in dollars per share) | $ / shares $ 3.59   $ 3.59      
Share based compensation, shares authorized under significant ranges of outstanding stock option plans in period [Abstract]            
Total Number of Options (in shares) 10,466,306   10,466,306      
Weighted-Average Remaining Contractual Life     8 years 1 month 28 days      
Weighted-Average Exercise Price (in dollars per share) | $ / shares $ 3.33   $ 3.33      
Total Number of Options Exercisable (in shares) 6,911,989   6,911,989      
Weighted-Average Remaining Contractual Life     7 years 8 months 26 days      
Weighted-Average Exercise Price, Options Exercisable (in dollars per share) | $ / shares $ 3.59   $ 3.59      
The aggregate intrinsic value of outstanding options | $ $ 10,200,000   $ 10,200,000      
Aggregate intrinsic value of options vested | $     $ 6,100,000      
Closing price of the common stock (in dollars per share) | $ / shares $ 3.72   $ 3.72      
Stock Options [Member] | Employees [Member]            
Number of Options (Employees and Non-Employees) [Abstract]            
Outstanding at beginning of period (in shares)     9,348,952      
Granted (in shares)     550,000      
Expired (in shares)     (68,000)      
Outstanding at end of period (in shares) 9,830,952   9,830,952      
Options exercisable at end of period (in shares) 6,276,275   6,276,275      
Stock Options [Member] | Non-Employees [Member]            
Number of Options (Employees and Non-Employees) [Abstract]            
Outstanding at beginning of period (in shares)     692,143      
Granted (in shares)     0      
Expired (in shares)     (56,429)      
Outstanding at end of period (in shares) 635,714   635,714      
Options exercisable at end of period (in shares) 635,714   635,714      
Stock Options And Warrants [Member]            
Share-based compensation arrangement by share-based payment award, fair value assumptions and methodology [Abstract]            
Risk-free interest rate (in hundredths)     2.21% 1.92%    
Expected dividend yield (in hundredths)     0.00% 0.00%    
Stock Options And Warrants [Member] | Minimum [Member]            
Share-based compensation arrangement by share-based payment award, fair value assumptions and methodology [Abstract]            
Expected volatility (in hundredths)     78.20% 87.00%    
Expected lives     6 years 6 years    
Stock Options And Warrants [Member] | Maximum [Member]            
Share-based compensation arrangement by share-based payment award, fair value assumptions and methodology [Abstract]            
Expected volatility (in hundredths)     84.40% 89.60%    
Expected lives     10 years 10 years    
Stock Options And Warrants [Member] | Employees [Member]            
Total stock-based compensation expense resulting from stock options and warrants [Abstract]            
Allocated employee and non-employee stock-based compensation expense, Total | $ $ 2,137,282 $ 559,863 $ 3,428,624 $ 1,046,977    
Stock Options And Warrants [Member] | Non-Employees [Member]            
Total stock-based compensation expense resulting from stock options and warrants [Abstract]            
Allocated employee and non-employee stock-based compensation expense, Total | $ 140,533 160,629 234,084 352,620    
Restricted Stock [Member]            
Total stock-based compensation expense resulting from stock options and warrants [Abstract]            
Allocated employee and non-employee stock-based compensation expense, Total | $ $ 0 $ 156,296 $ 0 $ 310,874    
Warrants [Member]            
Weighted-Average Exercise Price Options [Abstract]            
Share-based compensation arrangement by share-based payment award, shares issued in period (in shares)       25,000    
Exercise price of warrants (in dollars per share) | $ / shares   $ 5.60   $ 5.60    
Share based compensation, shares authorized under significant ranges of outstanding stock option plans in period [Abstract]            
Warrants outstanding (in shares) 7,282,617   7,282,617   7,349,760  
Weighted-average exercise price of warrants outstanding (in dollars per share) | $ / shares 4.29   4.29   4.27  
Range $ 1.83 - 2.50 [Member] | Stock Options [Member]            
Share based compensation, shares authorized under significant ranges of outstanding stock option plans in period [Abstract]            
Range of Exercise Prices, Lower Range (in dollars per share) | $ / shares     $ 1.83      
Range of Exercise Prices, Upper Range (in dollars per share) | $ / shares     $ 2.50      
Total Number of Options (in shares) 5,837,558   5,837,558      
Weighted-Average Remaining Contractual Life     8 years 6 months 4 days      
Weighted-Average Exercise Price (in dollars per share) | $ / shares $ 2.12   $ 2.12      
Total Number of Options Exercisable (in shares) 3,226,398   3,226,398      
Weighted-Average Remaining Contractual Life     8 years      
Weighted-Average Exercise Price, Options Exercisable (in dollars per share) | $ / shares $ 2.08   $ 2.08      
Range $ 2.51 - 3.50 [Member] | Stock Options [Member]            
Share based compensation, shares authorized under significant ranges of outstanding stock option plans in period [Abstract]            
Range of Exercise Prices, Lower Range (in dollars per share) | $ / shares     2.51      
Range of Exercise Prices, Upper Range (in dollars per share) | $ / shares     $ 3.50      
Total Number of Options (in shares) 954,482   954,482      
Weighted-Average Remaining Contractual Life     8 years 7 months 20 days      
Weighted-Average Exercise Price (in dollars per share) | $ / shares $ 2.85   $ 2.85      
Total Number of Options Exercisable (in shares) 874,482   874,482      
Weighted-Average Remaining Contractual Life     8 years 7 months 13 days      
Weighted-Average Exercise Price, Options Exercisable (in dollars per share) | $ / shares $ 2.83   $ 2.83      
Range $ 3.51 - 8.00 [Member] | Stock Options [Member]            
Share based compensation, shares authorized under significant ranges of outstanding stock option plans in period [Abstract]            
Range of Exercise Prices, Lower Range (in dollars per share) | $ / shares     3.51      
Range of Exercise Prices, Upper Range (in dollars per share) | $ / shares     $ 8.00      
Total Number of Options (in shares) 3,386,201   3,386,201      
Weighted-Average Remaining Contractual Life     7 years 11 months 5 days      
Weighted-Average Exercise Price (in dollars per share) | $ / shares $ 5.06   $ 5.06      
Total Number of Options Exercisable (in shares) 2,523,043   2,523,043      
Weighted-Average Remaining Contractual Life     7 years 8 months 26 days      
Weighted-Average Exercise Price, Options Exercisable (in dollars per share) | $ / shares $ 5.16   $ 5.16      
Range $ 8.01 - 32.55 [Member] | Stock Options [Member]            
Share based compensation, shares authorized under significant ranges of outstanding stock option plans in period [Abstract]            
Range of Exercise Prices, Lower Range (in dollars per share) | $ / shares     8.01      
Range of Exercise Prices, Upper Range (in dollars per share) | $ / shares     $ 32.55      
Total Number of Options (in shares) 288,065   288,065      
Weighted-Average Remaining Contractual Life     2 years 3 months 22 days      
Weighted-Average Exercise Price (in dollars per share) | $ / shares $ 9.00   $ 9.00      
Total Number of Options Exercisable (in shares) 288,066   288,066      
Weighted-Average Remaining Contractual Life     2 years 3 months 22 days      
Weighted-Average Exercise Price, Options Exercisable (in dollars per share) | $ / shares $ 9.00   $ 9.00      
Research and Development Expense [Member] | Stock Options And Warrants [Member] | Employees [Member]            
Total stock-based compensation expense resulting from stock options and warrants [Abstract]            
Allocated employee and non-employee stock-based compensation expense, Total | $ $ 392,842 $ 234,484 $ 728,780 $ 409,638    
Research and Development Expense [Member] | Stock Options And Warrants [Member] | Non-Employees [Member]            
Total stock-based compensation expense resulting from stock options and warrants [Abstract]            
Allocated employee and non-employee stock-based compensation expense, Total | $ 0 0 0 0    
General and Administrative Expense [Member] | Stock Options And Warrants [Member] | Employees [Member]            
Total stock-based compensation expense resulting from stock options and warrants [Abstract]            
Allocated employee and non-employee stock-based compensation expense, Total | $ 1,744,440 325,379 2,699,844 637,339    
General and Administrative Expense [Member] | Stock Options And Warrants [Member] | Non-Employees [Member]            
Total stock-based compensation expense resulting from stock options and warrants [Abstract]            
Allocated employee and non-employee stock-based compensation expense, Total | $ $ 140,533 $ 160,629 $ 234,084 $ 352,620    
2000 Long Term Incentive Plan [Member]            
Share-based Compensation Arrangement by Share-based Payment Award [Line Items]            
Share-based compensation, shares subject to stock options (in shares) 600,000   600,000      
Expiration date     Aug. 06, 2010      
Share-based compensation, shares available for future grant (in shares) 0   0      
2008 Stock Incentive Plan [Member]            
Share-based Compensation Arrangement by Share-based Payment Award [Line Items]            
Share-based compensation, shares subject to stock options (in shares) 9,900,000   9,900,000      
Share-based compensation, shares available for future grant (in shares) 10,100,000   10,100,000      
2008 Stock Incentive Plan [Member] | Restricted Stock [Member] | Senior management [Member]            
Weighted-Average Exercise Price Options [Abstract]            
Restricted stock granted (in shares)     100,000      
Value of restricted shares issued | $ $ 627,000   $ 627,000      
XML 19 R30.htm IDEA: XBRL DOCUMENT v3.2.0.727
Liquidity and Capital Resources (Details) - USD ($)
6 Months Ended
Jul. 21, 2015
Feb. 05, 2014
Jun. 30, 2015
Dec. 31, 2014
Jun. 30, 2014
Dec. 31, 2013
Estimated projected expenditure [Line Items]            
Cash and cash equivalents     $ 38,833,736 $ 32,218,905 $ 51,866,891 $ 11,483,112
Short-term investments     15,002,213 $ 45,621,593    
Net proceeds received from underwritten public offering   $ 80,500,000        
Currently projected expenditures for clinical programs     54,000,000      
Subsequent Event [Member]            
Estimated projected expenditure [Line Items]            
Net proceeds received from underwritten public offering $ 26,800,000          
Aldoxorubicin [Member]            
Estimated projected expenditure [Line Items]            
Currently projected expenditures for clinical programs     37,000,000      
Other Programs [Member]            
Estimated projected expenditure [Line Items]            
Currently projected expenditures for clinical programs     2,300,000      
General Operation [Member]            
Estimated projected expenditure [Line Items]            
Currently projected expenditures for clinical programs     3,900,000      
Other General and Administrative Expenses [Member]            
Estimated projected expenditure [Line Items]            
Currently projected expenditures for clinical programs     $ 10,800,000      
XML 20 R31.htm IDEA: XBRL DOCUMENT v3.2.0.727
Equity Transactions (Details) - USD ($)
$ / shares in Units, $ in Millions
3 Months Ended 6 Months Ended
Apr. 27, 2015
Feb. 05, 2014
Jan. 01, 2014
Mar. 31, 2014
Jun. 30, 2015
Dec. 31, 2014
Mar. 15, 2014
Equity Transactions [Abstract]              
Common shares issued from the exercise of warrants (in shares) 5,211     278,000      
Restricted shares granted (in shares)     100,000        
Non-cash expense of shares issued         $ 0.6    
Stock issued, underwritten public offering, value   $ 86.0          
Stock issued, underwritten public offering, value (in shares)   13,200,000          
Common stock per share value (in dollars per share)   $ 6.50          
Net proceeds from issuance of common stock   $ 80.5          
Common stock, shares issued (in shares)         55,927,197 55,921,986 200,000
Warrants issued, rights (in shares) 10,000           25,000
Common stock, fair value             $ 0.8
Proceeds from the issuance of warrants       $ 0.4      
XML 21 R8.htm IDEA: XBRL DOCUMENT v3.2.0.727
Foreign Currency Remeasurement
6 Months Ended
Jun. 30, 2015
Foreign Currency Remeasurement [Abstract]  
Foreign Currency Remeasurement
3.           Foreign Currency Remeasurement
 
The U.S. dollar has been determined to be the functional currency for the net assets of the Company’s laboratory facility in Germany. The transactions are recorded in the local currencies and are remeasured at each reporting date using the historical rates for nonmonetary assets and liabilities and exchange rates for monetary assets and liabilities at the balance sheet date. Exchange gains and losses from the remeasurement of monetary assets and liabilities are recognized in other income (loss). The Company recognized a gain of approximately $5,000 and a loss of approximately $10,700 for the three-month and six-month periods ended June 30, 2015, respectively, and $0 and $4,900 for the three and six-month periods ended June 30, 2014, respectively.
XML 22 R32.htm IDEA: XBRL DOCUMENT v3.2.0.727
Income Taxes (Details) - USD ($)
$ in Millions
3 Months Ended
Jun. 30, 2015
Dec. 31, 2014
Minimum [Member]    
Operating Loss Carryforwards [Line Items]    
Operating loss carryforwards, expiration date Dec. 31, 2015  
Maximum [Member]    
Operating Loss Carryforwards [Line Items]    
Operating loss carryforwards, expiration date Dec. 31, 2034  
Federal [Member]    
Operating Loss Carryforwards [Line Items]    
Operating loss carryforwards   $ 227.5
Operating loss carryforwards, unrestricted   165.2
State [Member]    
Operating Loss Carryforwards [Line Items]    
Operating loss carryforwards   157.5
Operating loss carryforwards, unrestricted   $ 157.5
XML 23 R2.htm IDEA: XBRL DOCUMENT v3.2.0.727
CONDENSED BALANCE SHEETS (Unaudited) - USD ($)
Jun. 30, 2015
Dec. 31, 2014
Current assets:    
Cash and cash equivalents $ 38,833,736 $ 32,218,905
Short-term investments 15,002,213 45,621,593
Receivables 5,175,007 2,019,293
Interest receivable 14,196 104,627
Prepaid expenses and other current assets 976,325 3,250,355
Total current assets 60,001,477 83,214,773
Equipment and furnishings, net 879,359 970,873
Goodwill 183,780 183,780
Other assets 1,569,193 1,323,156
Total assets 62,633,809 85,692,582
Current liabilities:    
Accounts payable 5,328,351 6,655,962
Accrued expenses and other current liabilities 10,376,415 5,994,072
Warrant liability 4,566,515 5,131,085
Total current liabilities $ 20,271,281 $ 17,781,119
Commitments and contingencies    
Stockholders' equity    
Preferred Stock, $0.01 par value, 5,000,000 shares authorized, including 25,000 shares of Series A Junior Participating Preferred Stock; no shares issued and outstanding $ 0 $ 0
Common stock, $0.001 par value, 250,000,000 shares authorized; 55,927,197 shares issued and outstanding at June 30, 2015; 55,921,986 shares issued and outstanding at December 31, 2014 55,927 55,924
Additional paid-in capital 380,638,689 376,975,984
Treasury stock, at cost (199,275 shares) (2,612,861) (2,612,861)
Accumulated deficit (335,719,227) (306,507,584)
Total stockholders' equity 42,362,528 67,911,463
Total liabilities and stockholders' equity $ 62,633,809 $ 85,692,582
XML 24 R6.htm IDEA: XBRL DOCUMENT v3.2.0.727
Description of Company and Basis of Presentation
6 Months Ended
Jun. 30, 2015
Description of Company and Basis of Presentation [Abstract]  
Description of Company and Basis of Presentation
1.  Description of Company and Basis of Presentation
 
CytRx Corporation (“CytRx” or the “Company”) is a biopharmaceutical research and development company specializing in oncology. The Company is currently focused on the clinical development of aldoxorubicin (formerly known as INNO-206), its modified version of the widely-used chemotherapeutic agent, doxorubicin. CytRx previously reported positive top-line efficacy results (median progression-free survival, or PFS, PFS at six months, overall response rates, hazard ratios and overall survival) from its completed, global Phase 2b clinical trial with aldoxorubicin as a treatment for soft tissue sarcoma, or STS. Hazard ratios, or the likelihood that the study endpoint (in this case tumor progression) will be reached during a given period, are an important measure of the reliability and uniformity of the absolute data for PFS. The trial investigated the efficacy and safety of aldoxorubicin compared with doxorubicin in subjects with first-line metastatic, locally advanced or unresectable STS. Aldoxorubicin combines the chemotherapeutic agent doxorubicin with a novel linker-molecule that binds specifically to albumin in the blood and is designed to allow for delivery of higher amounts of doxorubicin (3½ to 4 times) without the major dose-limiting toxicities as seen with the administration of doxorubicin alone.
 
In the first quarter of 2014, the Company initiated a pivotal Phase 3 trial of aldoxorubicin as a therapy for patients with STS whose tumors have progressed following treatment with chemotherapy. The Phase 3 trial is being conducted under a Special Protocol Assessment, or SPA, granted by the FDA. The SPA means that the FDA agrees that the design and analyses proposed in the Phase 3 trial protocol are acceptable to support regulatory approval of the product candidate with respect to effectiveness of the indication studied, and will not change its perspective on these matters, except in limited circumstances such as where a sponsor fails to follow a protocol agreed to with the FDA or where previously unrecognized health concerns occur.  Thus, if the study demonstrates an acceptable benefit-risk profile as determined by the FDA, it will support registration of aldoxorubicin for this indication.  If approved for marketing, the Company’s current plan would be to commercially launch aldoxorubicin in late 2017.
 
CytRx is currently evaluating aldoxorubicin in a global Phase 2b clinical trial in small cell lung cancer, a Phase 2 clinical trial in HIV-related Kaposi's sarcoma, a Phase 2 clinical trial in patients with late-stage glioblastoma (brain cancer), a Phase 1b clinical trial in combination with ifosfamide in patients with STS and a Phase 1b clinical trial in combination with gemcitabine in patients with metastatic solid tumors. The Company has completed a global Phase 2b clinical trial with aldoxorubicin as a 1st-line therapy for STS, a Phase 1b/2 clinical trial primarily in the same indication, a Phase 1b clinical trial of aldoxorubicin in combination with doxorubicin in patients with advanced solid tumors and a Phase 1b pharmacokinetics clinical trial in patients with metastatic solid tumors.
 
CytRx plans to expand its pipeline of oncology candidates through its drug-development activities at its laboratory facility in Freiburg, Germany, based on its Linker Activated Drug Release, or LADR™, technology that can be utilized with multiple chemotherapeutic agents and may allow for greater drug concentration at tumor sites.
 
The accompanying condensed financial statements at June 30, 2015 and for the three-month and six-month periods ended June 30, 2015 and 2014, respectively, are unaudited, but include all adjustments, consisting of normal recurring entries, that management believes to be necessary for a fair presentation of the periods presented. Interim results are not necessarily indicative of results for a full year. Balance sheet amounts as of December 31, 2014 have been derived from the Company’s audited financial statements as of that date.
 
The financial statements included herein have been prepared by the Company pursuant to the rules and regulations of the Securities and Exchange Commission (“SEC”). Certain information and footnote disclosures normally included in financial statements prepared in accordance with accounting principles generally accepted in the United States of America have been condensed or omitted pursuant to such rules and regulations. The financial statements should be read in conjunction with the Company’s audited financial statements contained in its Annual Report on Form 10-K for the year ended December 31, 2014. The Company’s operating results will fluctuate for the foreseeable future. Therefore, period-to-period comparisons should not be relied upon as predictive of the results in future periods.
XML 25 R22.htm IDEA: XBRL DOCUMENT v3.2.0.727
Subsequent Events (Tables)
6 Months Ended
Jun. 30, 2015
Subsequent Events [Abstract]  
Schedule of selected pro forma balance sheet data
The following selected pro forma balance sheet data is derived from our balance sheet as of June 30, 2015 and gives retroactive effect to the completion of the underwritten offering, but does not give effect to other events that occurred since June 30, 2015  and thus may not be indicative of our current financial condition. The information should be read in conjunction with our balance sheet as of June 30, 2015  and related notes.
 
   
Actual as of June 30, 2015 (unaudited)
  
Adjustments Related to July 2015 Equity Financing (unaudited)
  
Pro Forma as of June 30, 2015 (unaudited)
 
ASSETS
         
           
Current assets:
         
Cash and cash equivalents
 $38,833,736  $26,752,025  $65,585,761 
Short-term investments
  15,002,213      15,002,213 
Prepaid and other current assets
  6,165,528      6,165,528 
    Total current assets
  60,001,477   26,752,025   86,753,502 
Non-current assets
  2,632,332      2,632,332 
Total assets
 $62,633,809  $26,752,025  $89,385,834 
              
LIABILITIES AND STOCKHOLDERS’ EQUITY
            
              
Current liabilities:            
     Accounts payable and other current liabilities                  $15,704,766      $15,704,766  
     Warrant liability $    4,566,515       $4,566,515  
Total current liabilities
 $20,271,281  $  $20,271,281 

Stockholders’ equity:
         
           
 Common stock
 $55,927  $10,465  $66,392 
   Additional paid-in-capital
  380,638,689   26,741,560   407,380,249 
   Treasury stock
  (2,612,861)     (2,612,861)
   Accumulated deficit
  (335,719,227)     (335,719,227)
Total stockholders’ equity
  42,362,528   26,752,025   69,114,553 
Total liabilities and stockholders’ equity
 $62,633,809  $26,752,025  $89,385,834 
XML 26 R24.htm IDEA: XBRL DOCUMENT v3.2.0.727
Foreign Currency Remeasurement (Details) - USD ($)
3 Months Ended 6 Months Ended
Jun. 30, 2015
Jun. 30, 2014
Jun. 30, 2015
Jun. 30, 2014
Foreign Currency Remeasurement [Abstract]        
(Gain) loss on foreign currency translation adjustment $ 5,000 $ 0 $ (10,700) $ (4,900)
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Recent Accounting Pronouncements
6 Months Ended
Jun. 30, 2015
Recent Accounting Pronouncements [Abstract]  
Recent Accounting Pronouncements
2.           Recent Accounting Pronouncements
 
We have reviewed all of the recent accounting pronouncements and have determined that they have not or will not have a material impact on the Company’s financial statements, or simply do not apply to the Company’s operations.
XML 29 R3.htm IDEA: XBRL DOCUMENT v3.2.0.727
CONDENSED BALANCE SHEETS (Unaudited) (Parenthetical) - $ / shares
Jun. 30, 2015
Dec. 31, 2014
Stockholders' equity    
Preferred Stock, par value (in dollars per share) $ 0.01 $ 0.01
Preferred Stock, shares authorized (in shares) 5,000,000 5,000,000
Series A Junior Participating Preferred Stock, shares authorized (in shares) 25,000 25,000
Preferred Stock, shares issued (in shares) 0 0
Preferred Stock, shares outstanding (in shares) 0 0
Common stock, par value (in dollars per share) $ 0.001 $ 0.001
Common stock, shares authorized (in shares) 250,000,000 250,000,000
Common stock, shares issued (in shares) 55,927,197 55,921,986
Common stock, shares outstanding (in shares) 55,927,197 55,921,986
Treasury stock (in shares) 199,275 199,275
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Commitments and contingencies
6 Months Ended
Jun. 30, 2015
Commitments and contingencies [Abstract]  
Commitments and contingencies
12.           Commitments and Contingencies
 
Commitments
 
The Company has an agreement with KTB for the Company’s exclusive license of patent rights held by KTB for the worldwide development and commercialization of aldoxorubicin. Under the agreement, the Company must make payments to KTB in the aggregate of $7.5 million upon meeting clinical and regulatory milestones up to and including the product’s second final marketing approval. In the six months ended June 30, 2014, the Company met two clinical milestones, resulting in total payments of $2.0 million to KTB.  The Company also has agreed to pay:
 
·  
commercially reasonable royalties based on a percentage of net sales (as defined in the agreement);
 
·  
a percentage of non-royalty sub-licensing income (as defined in the agreement); and
 
·  
milestones of $1 million for each additional final marketing approval that the Company obtains.
 
In the event that the Company must pay a third party in order to exercise its rights to the intellectual property under the agreement, the Company will deduct a percentage of those payments from the royalties due KTB, up to an agreed upon cap.
 
-9- 

Contingencies
 
On June 13, 2014, three purported securities class action lawsuits pending in the United States District Court for the Central District of California, were consolidated in the matter of In re CytRx Corporation Securities Litigation, 2:14-CV-01956-GHK (PJWx), and lead plaintiff and lead counsel were appointed. On October 1, 2014, plaintiffs filed a consolidated amended complaint on behalf of all persons who purchased or otherwise acquired the publicly traded securities of CytRx between November 20, 2013 and March 13, 2014, against CytRx, certain Company officers and directors, a freelance writer, and certain underwriters. The complaint alleges that certain of the defendants violated the Securities Exchange Act of 1934 by making materially false and misleading statements in press releases, promotional articles, SEC filings and other public statements. The complaint further alleges that certain of the defendants violated the Securities Act of 1933 by making materially misleading statements and omitting material information in the shelf Registration Statement on Form S-3 filed with the SEC on December 6, 2012 and Prospectus Supplement on Form 424(b)(2) filed with the SEC on January 31, 2014. These allegations arise out of the Company’s alleged retention of The DreamTeam Group and MissionIR, external investor and public relations firms unaffiliated with the Company, as well as the Company’s December 9, 2013 grant of stock options to certain board members and officers. The consolidated amended complaint seeks damages, including interest, in an unspecified amount, reasonable costs and attorneys’ fees, and any equitable, injunctive, or other relief that the court may deem just and proper.  On December 5, 2014, CytRx and the individual defendants filed a motion to dismiss the complaint.  The Court was scheduled to hear argument on this motion on March 2, 2015.  On February 25, 2015, the Court took this motion under submission and took the hearing off calendar. On July 13, 2015, the Court issued an order granting in part and denying in part the motions to dismiss filed by us, the individual defendants and the underwriters. The Court afforded the plaintiffs 30 days to amend their complaint, if they elect to do so.
 
    On April 3, 2014, a purported class action lawsuit was filed against the Company and certain of its officers and each of its directors, as well as certain underwriters, in the Superior Court of California, County of Los Angeles, captioned Rajasekaran v. CytRx Corporation, et al., BC541426. The complaint purports to be brought on behalf of all shareholders who purchased or otherwise acquired the Company’s common stock pursuant or traceable to its public offering that closed on February 5, 2014. The complaint alleges that defendants violated the federal securities laws by making materially false and misleading statements in the Company’s filings with the SEC. The complaint seeks compensatory damages in an unspecified amount, rescission, and attorney’s fees and costs. On October 14, 2014, the Court granted the parties’ joint ex parte motion to stay this proceeding pending resolution of motions to dismiss in the related federal action,  In re CytRx Corporation Securities Litigation , 2:14-CV-01956-GHK (PJWx).
 
    On July 3, 2014, a shareholder derivative lawsuit was filed in the United States District Court for the Central District of California, captioned  Fishman v. Kriegsman, et al. , 2:14-cv-05169, purportedly on the Company’s behalf against certain of its officers and each of its directors. The complaint alleges breach of fiduciary duties, corporate waste, gross mismanagement, and unjust enrichment in connection with the Company’s alleged retention of DreamTeamGroup and MissionIR. The complaint seeks damages, restitution, corporate governance reforms, and attorney’s fees and costs. On September 3, 2014, plaintiff filed a notice to voluntarily dismiss this action against all parties without prejudice, which the Court granted on September 9, 2014.
 
    On September 10, 2014, the Delaware Court of Chancery consolidated Schwartz v. Ignarro, et al., Case No. 9864, Johnson v. Ignarro, et al. , Case No. 9884, and  Silverberg v. Kriegsman, et al. , Case No. 9919, three shareholder derivative lawsuits described in the Company’s Quarterly Report filed with the SEC on August 6, 2014. The allegations in the  Schwartz  and  Johnson complaints relate to the Company’s December 9, 2013 grant of stock options to certain board members and officers. The allegations in the  Silverberg  complaint relate to the Company’s December 9, 2013 grant of stock options to certain board members and officers, as well as its alleged retention of DreamTeamGroup and MissionIR. A consolidated complaint concentrated on the stock-option grant claims was filed on October 9, 2014. The consolidated lawsuit is captioned  In re CytRx Corp. Stockholder Derivative Litigation,  C.A. No. 9864-VCL. On November 10, 2014, the Company and the individual defendants filed a motion to dismiss the consolidated complaint or, in the alternative, to stay the action. The Court heard argument on the motions on January 8, 2015. The Court denied the motion to dismiss and granted in part and denied in part the motion to stay.
 
-10- 

    On June 2, 2015, the Company announced that they had reached an agreement to settle the Delaware stockholder derivative action. Under the settlement, it agreed to re-price certain stock options to purchase common stock that were granted on December 10, 2013 to certain of its directors and officers from the original exercise price of $2.39 to an exercise price of $4.66 (the share price at market closing on December 20, 2013). The settlement also provides that the Company will implement certain corporate governance changes and modify its governance practices regarding the granting of stock options. The parties have reached an agreement on an award of $1.1 million of fees and expenses to plaintiffs’ attorneys, which award must be approved by the Court regardless of whether there is an agreement between the parties. These fees and expenses will be covered by the Company’s insurance companies. The settlement is subject to the drafting of definitive documentation, notice to stockholders, and Court approval.
 
    On August 14, 2014, a shareholder derivative lawsuit, captioned Pankratz v. Kriegsman, et al., 2:14-cv-06414-PA-JPR, was filed in the United States District Court for the Central District of California purportedly on the Company’s behalf against certain of its officers and each of its directors. The complaint alleges breach of fiduciary duties, unjust enrichment, gross mismanagement, abuse of control, insider selling and misappropriation of information in connection with the Company’s alleged retention of DreamTeamGroup and MissionIR, as well as its December 9, 2013 grant of stock options to certain board members and officers. The complaint seeks unspecified damages, corporate governance and internal procedures reforms, restitution, disgorgement of all profits, benefits, and other compensation obtained by the individual defendants, and the costs and disbursements of the action.
 
    On August 15, 2014, a shareholder derivative complaint, captioned Taylor v. Kriegsman, et al., 2:14-cv-06451, was filed in the United States District Court for the Central District of California purportedly on the Company’s behalf against certain of its officers and each of its directors. The complaint alleges breach of fiduciary duties, unjust enrichment, gross mismanagement, abuse of control, unjust enrichment, insider selling and misappropriation of information in connection with the Company’s alleged retention of DreamTeamGroup and MissionIR, as well as its December 9, 2013 grant of stock options to certain board members and officers. The complaint seeks unspecified damages, corporate governance and internal procedures reforms, restitution, disgorgement of all profits, benefits, and other compensation obtained by the individual defendants, and the costs and disbursements of the action.
 
    On October 8, 2014, the Court in Pankratz and Taylor consolidated the cases and appointed lead plaintiffs and co-lead counsel. On October 20, 2014, the Company and the individual defendants filed motions to dismiss the consolidated  Pankratz  and Taylor  cases or, in the alternative, to stay the cases. On January 9, 2015, the Court stayed the action pending the resolution of the consolidated Delaware derivative action. On February 27, 2015, the  Pankratz  and  Taylor  plaintiffs filed a motion to vacate the stay. On June 24, 2015, the Court granted the motion to lift the stay in light of the pending settlement of the Delaware derivative litigation discussed above. The Court further denied the motion to dismiss without prejudice and invited the Company to move to dismiss the case within 30 days pursuant to the doctrine of  forum non conveniens  based on its forum-selection bylaw, which mandates that derivative actions be filed in Delaware. The Court advised that it would consider any  forum non conveniens  motion before considering a subsequent motion to dismiss under Rule 12.

    The Company intends to vigorously defend against the foregoing complaints. The Company has directors’ and officers’ liability insurance, which will be utilized in the defense of these matters. The Company has incurred legal expenses in defending these complaints and as of June 30, 2015, the Company has an outstanding receivable from its insurance carrier of $5.2 million related to these expenses. The liability insurance may not cover all of the future liabilities the Company may incur in connection with the foregoing matters. These claims are subject to inherent uncertainties, and managements’s views of these matters may change in the future.

    The Company evaluates developments in legal proceedings and other matters on a quarterly basis. If an unfavorable outcome becomes probable and reasonably estimable, the Company could incur charges that could have a material adverse impact on the Comapny’s financial condition and results of operations for the period in which the outcome becomes probable and reasonably estimable.

XML 32 R1.htm IDEA: XBRL DOCUMENT v3.2.0.727
Document and Entity Information - shares
6 Months Ended
Jun. 30, 2015
Aug. 03, 2015
Document and Entity Information [Abstract]    
Entity Registrant Name CYTRX CORP  
Entity Central Index Key 0000799698  
Current Fiscal Year End Date --12-31  
Entity Well-known Seasoned Issuer No  
Entity Voluntary Filers No  
Entity Current Reporting Status Yes  
Entity Filer Category Accelerated Filer  
Entity Common Stock, Shares Outstanding   66,480,065
Document Fiscal Year Focus 2015  
Document Fiscal Period Focus Q2  
Document Type 10-Q  
Amendment Flag false  
Document Period End Date Jun. 30, 2015  
XML 33 R18.htm IDEA: XBRL DOCUMENT v3.2.0.727
Subsequent Events
6 Months Ended
Jun. 30, 2015
Subsequent Events [Abstract]  
Subsequent Events
13. Subsequent Events
 
On July 24, 2015, the Company completed a $28.7 million underwritten public offering, in which it sold and issued 10,465,000 shares of common stock at a price of $2.75 per share. Net of underwriting discounts, legal, accounting and other offering expenses, the Company received proceeds of approximately $26.8 million, exclusive of treasury shares.
 
The following selected pro forma balance sheet data is derived from our balance sheet as of June 30, 2015 and gives retroactive effect to the completion of the underwritten offering, but does not give effect to other events that occurred since June 30, 2015  and thus may not be indicative of our current financial condition. The information should be read in conjunction with our balance sheet as of June 30, 2015  and related notes.
 
   
Actual as of June 30, 2015 (unaudited)
  
Adjustments Related to July 2015 Equity Financing (unaudited)
  
Pro Forma as of June 30, 2015 (unaudited)
 
ASSETS
         
           
Current assets:
         
Cash and cash equivalents
 $38,833,736  $26,752,025  $65,585,761 
Short-term investments
  15,002,213      15,002,213 
Prepaid and other current assets
  6,165,528      6,165,528 
    Total current assets
  60,001,477   26,752,025   86,753,502 
Non-current assets
  2,632,332      2,632,332 
Total assets
 $62,633,809  $26,752,025  $89,385,834 
              
LIABILITIES AND STOCKHOLDERS’ EQUITY
            
              
Current liabilities:            
     Accounts payable and other current liabilities                  $15,704,766      $15,704,766  
     Warrant liability $    4,566,515       $4,566,515  
Total current liabilities
 $20,271,281  $  $20,271,281 

Stockholders’ equity:
         
           
 Common stock
 $55,927  $10,465  $66,392 
   Additional paid-in-capital
  380,638,689   26,741,560   407,380,249 
   Treasury stock
  (2,612,861)     (2,612,861)
   Accumulated deficit
  (335,719,227)     (335,719,227)
Total stockholders’ equity
  42,362,528   26,752,025   69,114,553 
Total liabilities and stockholders’ equity
 $62,633,809  $26,752,025  $89,385,834 
XML 34 R4.htm IDEA: XBRL DOCUMENT v3.2.0.727
CONDENSED STATEMENTS OF OPERATIONS (Unaudited) - USD ($)
3 Months Ended 6 Months Ended
Jun. 30, 2015
Jun. 30, 2014
Jun. 30, 2015
Jun. 30, 2014
Revenue:        
License revenue $ 0 $ 0 $ 0 $ 0
Expenses:        
Research and development 10,008,304 10,427,877 22,573,181 17,415,725
General and administrative 4,191,769 2,909,127 7,322,001 6,040,201
Total expenses 14,200,073 13,337,004 29,895,182 23,455,926
Loss before other income (loss) (14,200,073) (13,337,004) (29,895,182) (23,455,926)
Other income (loss):        
Interest income 46,455 89,377 103,029 160,015
Other income (loss), net 30,660 (3,243) 15,940 6,655
Gain (loss) on warrant derivative liability 2,435,865 (2,468,603) 564,570 12,234,301
Net loss $ (11,687,093) $ (15,719,473) $ (29,211,643) $ (11,054,955)
Basic and diluted net loss per share (in dollars per share) $ (0.21) $ (0.28) $ (0.52) $ (0.21)
Basic and diluted weighted-average shares outstanding (in shares) 55,726,432 55,676,766 55,724,581 53,010,556
XML 35 R12.htm IDEA: XBRL DOCUMENT v3.2.0.727
Stock Based Compensation
6 Months Ended
Jun. 30, 2015
Stock Based Compensation [Abstract]  
Stock Based Compensation
7.           Stock Based Compensation
 
The Company has a 2000 Long-Term Incentive Plan, which expired on August 6, 2010.  As of June 30, 2015, there were approximately 0.6 million shares subject to outstanding stock options under this plan.  No further shares are available for future grant under this plan.
 
The Company also has a 2008 Stock Incentive Plan.  As of June 30, 2015, there were 9.9 million shares subject to outstanding stock options and 10.1 million shares available for future grant under this plan.
 

-5- 


The Company follows ASC 718, Compensation-Stock Compensation, which requires the measurement and recognition of compensation expense for all stock-based awards made to employees.
 
For stock options and stock warrants paid in consideration of services rendered by non-employees, the Company recognizes compensation expense in accordance with the requirements of ASC 505-50.
 
Non-employee option grants that do not vest immediately upon grant are recorded as an expense over the vesting period. At the end of each financial reporting period, the value of these options, as calculated using the Black-Scholes option-pricing model, is determined, and compensation expense recognized or recovered during the period is adjusted accordingly. As a result, the amount of the future compensation expense is subject to adjustment until the common stock options are fully vested.
 
The following table sets forth the total stock-based compensation expense resulting from stock options and warrants included in the Company’s unaudited interim statements of operations:
 
   
Three Months Ended June 30,
  
Six Months Ended June 30,
 
   
2015
  
2014
  
2015
  
2014
 
Research and development — employee
 $392,842  $234,484  $728,780  $409,638 
General and administrative — employee
  1,744,440   325,379   2,699,844   637,339 
Total employee stock-based compensation
 $2,137,282  $559,863  $3,428,624  $1,046,977 
                  
Research and development — non-employee
 $  $  $  $ 
General and administrative — non-employee
  140,533   160,629   234,084   352,620 
 Total non-employee stock-based compensation
 $140,533  $160,629  $234,084  $352,620 

During the six-month period ended June 30, 2015, the Company granted stock options to purchase 550,000 shares of its common stock. During the six-month period ended June 30, 2014, the Company granted stock options to purchase 300,000 shares of its common stock and issued warrants to purchase 25,000 shares of its stock with an exercise price of $5.60.The fair value of the stock options was estimated using the Black-Scholes option-pricing model, based on the following assumptions:
 
 
 
Six Months Ended June 30, 2015
  
Six Months Ended June 30, 2014
 
Risk-free interest rate
  2.21%  1.92%
Expected volatility
  78.2% - 84.4%  87.0% - 89.6%
Expected lives (years)
  6 - 10   6 - 10 
Expected dividend yield
  0.00%  0.00%
 
The Company’s computation of expected volatility is based on the historical daily volatility of its publicly traded stock.  The Company uses historical information to compute expected lives. In the six-month period ended June 30, 2015, the contractual term of the options granted was ten years. The dividend yield assumption of zero is based upon the fact the Company has never paid cash dividends and presently has no intention to do so.  The risk-free interest rate used for each grant and issuance is equal to the U.S. Treasury rates in effect at the time of the grant and issuance for instruments with a similar expected life. Based on historical experience, for the six-month period ended June 30, 2015, the Company estimated annualized forfeiture rates of 10% for options granted to its employees, 2% for options granted to senior management and 0% for options granted to directors and non-employees and for warrants issued to non-employees.  For the six-month period ended June 30, 2014, the Company estimated annualized forfeiture rates of 12% for options granted to its employees, 2% for options granted to senior management and 0% for options granted to directors and non-employees.  Compensation costs will be adjusted for future changes in estimated forfeitures.  The Company will record additional expense if the actual forfeitures are lower than estimated and will record a recovery of prior expense if the actual forfeiture rates are higher than estimated.
 
-6- 

As of June 30, 2015, there remained approximately $4.9 million of unrecognized compensation expense related to unvested stock options granted to current and former employees, directors, to be recognized as expense over a weighted-average period of 1.03 years. Presented below is the Company’s stock option activity:
 
 
 
Six Months Ended June 30, 2015
 
 
 
 
Number of Options (Employees)
  
Number of Options (Non-Employees)
  
Total Number
of Options
  
Weighted-Average Exercise Price
 
Outstanding at January 1, 2015
  9,348,952   692,143   10,040,735  $2.87 
Granted
  550,000      550,000  $3.86 
Expired
  (68,000)  (56,429)  (124,429) $6.90 
Outstanding at June 30, 2015
  9,830,952   635,714   10,466,306  $3.33 
Options exercisable at June 30, 2015
  6,276,275   635,714   6,911,989  $3.59 


The following table summarizes significant ranges of outstanding stock options under the Company’s plans at June 30, 2015:

Range of
 Exercise Prices
  
Total Number
of Options
  
Weighted-Average Remaining Contractual Life (years)
  
Weighted-Average Exercise Price
  
Total Number of Options Exercisable
  
Weighted-Average Remaining Contractual Life (years)
  
Weighted-Average Exercise Price
 
$1.83 - $2.50   5,837,558   8.51  $2.12   3,226,398   8.00  $2.08 
$2.51 – $3.50   954,482   8.64  $2.85   874,482   8.62  $2.83 
$3.51 – $8.00   3,386,201   7.93  $5.06   2,523,043   7.74  $5.16 
$8.01 – $32.55   288,065   2.31  $9.00   288,066   2.31  $9.00 
     10,466,306   8.16  $3.33   6,911,989   7.74  $3.59 

The aggregate intrinsic value of all outstanding options and vested options as of June 30, 2015 was $10.2 million and $6.1 million, respectively, representing options with exercise prices of less than the closing fair market value of the Company’s common stock on June 30, 2015 of $3.72 per share.
 
There were 7,282,617 and 7,349,760 warrants outstanding at June 30, 2015 and December 31, 2014, respectively at a weighted-average exercise price of $4.29 and $4.27, respectively.
 
Restricted Stock
 
On January 1, 2014, the Company granted to Dr. Daniel Levitt, Executive Vice President and Chief Medical Officer, 100,000 shares of CytRx Corporation restricted stock pursuant to the 2008 Plan, which shares have now fully vested.  The fair value of the restricted stock is based on the market price of the Company’s shares on the grant date less the par value received as consideration. The fair value of the restricted shares granted on January 1, 2014 was $627,000. The stock-based compensation expense relating to restricted stock included in the Company’s unaudited statements of operations for the three-month and six-month periods ended  June 30, 2014 was $156,296 and $310,874, respectively.  No restricted shares of common stock of the Company were granted in the comparable periods in 2015.
XML 36 R11.htm IDEA: XBRL DOCUMENT v3.2.0.727
Warrant Liabilities
6 Months Ended
Jun. 30, 2015
Warrant Liabilities [Abstract]  
Warrant Liabilities
6.           Warrant Liabilities
 
Liabilities measured at fair value on a recurring basis include warrant liabilities resulting from the Company’s past equity financings.  In accordance with ASC 815-40, Derivatives and Hedging – Contracts in Entity’s Own Equity (“ASC 815-40”), the warrant liabilities are being recorded at fair value until they are completely settled.  The warrants are valued using the Black-Scholes method, using assumptions consistent with the Company’s application of ASC 505-50, Equity-Based Payments to Non-Employees (“ASC 505-50”).  The gain or loss resulting from the change in fair value is shown on the Condensed Statements of Operations as gain (loss) on warrant derivative liability. The Company recognized a gain (loss) of $2.4 million and ($2.5) million for the three-month periods ended June 30, 2015 and 2014, respectively, and a gain of $0.6 million and $12.2 million for the six-month periods ended June 30, 2015 and 2014, respectively. The following reflects the weighted-average assumptions for each of the six-month periods indicated:
 
   
Six Months Ended June 30,
 
 
 
2015
  
2014
 
        
Risk-free interest rate
  0.28%  0.44%
Expected dividend yield
  0%  0%
Expected lives
  1.09   1.96 
    Expected volatility
  62.7%  84.1%
    Warrants classified as liabilities (in shares)
  6,371,854   6,984,716 
 
The Company’s computation of expected volatility is based on the historical daily volatility of its publicly traded stock. The dividend yield assumption of zero is based upon the fact that the Company has never paid cash dividends and presently has no intention to do so.  The risk-free interest rate used for each warrant classified as a derivative is equal to the U.S. Treasury rates in effect at June 30 of each year presented. The expected lives are based on the remaining contractual lives of the related warrants at the valuation date.
XML 37 R23.htm IDEA: XBRL DOCUMENT v3.2.0.727
Description of Company and Basis of Presentation (Details)
6 Months Ended
Jun. 30, 2015
Program
Description of Company and Basis of Presentation [Abstract]  
Number of programs in clinical development for cancer indications 2
XML 38 R19.htm IDEA: XBRL DOCUMENT v3.2.0.727
Warrant Liabilities (Tables)
6 Months Ended
Jun. 30, 2015
Warrant Liabilities [Abstract]  
Schedule of weighted-average assumptions
The following reflects the weighted-average assumptions for each of the six-month periods indicated:
 
   
Six Months Ended June 30,
 
 
 
2015
  
2014
 
        
Risk-free interest rate
  0.28%  0.44%
Expected dividend yield
  0%  0%
Expected lives
  1.09   1.96 
    Expected volatility
  62.7%  84.1%
    Warrants classified as liabilities (in shares)
  6,371,854   6,984,716 
XML 39 R15.htm IDEA: XBRL DOCUMENT v3.2.0.727
Equity Transactions
6 Months Ended
Jun. 30, 2015
Equity Transactions [Abstract]  
Equity Transactions
10.           Equity Transactions
 
On April 27, 2015, the Company issued 5,211 common shares pursant to a net exercise of warrants to purchase 10,000 shares.
 
On January 1, 2014, the Company granted 100,000 shares of restricted stock to Dr. Daniel Levitt, Executive Vice President and Chief Medical Officer (see Note 7), which resulted in non-cash expense of $0.6 million.
 
On February 5, 2014, the Company completed an $86.0 million underwritten public offering, in which it sold and issued 13.2 million shares of common stock at a price of $6.50 per share. Net of underwriting discounts, legal, accounting and other offering expenses, the Company received proceeds of approximately $80.5 million.
 
On March 15, 2014, the Company issued 200,000 common shares and warrants to purchase 25,000 common shares to KTB Tumorforschungs GmbH, or “KTB,” the licensor of aldoxorubicin, in connection with the establishment of the Company’s Freiburg, Germany research and development laboratory. The fair value of the shares was $0.8 million.
 
In the first quarter of 2014, the Company issued approximately 278,000 common shares for $0.4 million pursuant to the exercise of warrants.
XML 40 R13.htm IDEA: XBRL DOCUMENT v3.2.0.727
Fair Value Measurements
6 Months Ended
Jun. 30, 2015
Fair Value Measurements [Abstract]  
Fair Value Measurements
8.           Fair Value Measurements
 
Assets and liabilities recorded at fair value on the balance sheets are categorized based upon the level of judgment associated with the inputs used to measure the fair value.  Level inputs are as follows:
 
Level 1 – quoted prices in active markets for identical assets or liabilities.
 
Level 2 – other significant observable inputs for the assets or liabilities through corroboration with market data at the measurement date.
 
Level 3 – significant unobservable inputs that reflect management’s best estimate of what market participants would use to price the assets or liabilities at the measurement date.
 
The following table summarizes fair value measurements by level at June 30, 2015 for assets and liabilities measured at fair value on a recurring basis:
 
(In thousands)
 
Level I
  
Level II
  
Level III
  
Total
 
Cash equivalents
 $38,437  $  $  $38,437 
Short-term investments
  15,002         15,002 
Warrant liabilities
        (4,567)  (4,567)

The following table summarizes fair value measurements by level at December 31, 2014 for assets and liabilities measured at fair value on a recurring basis:
 
(In thousands)
 
Level I
  
Level II
  
Level III
  
Total
 
Cash equivalents
 $31,159  $  $  $31,159 
Short-term investments
  45,622         45,622 
Warrant liability
        (5,131)  (5,131)

Liabilities measured at market value on a recurring basis include warrant liability resulting from the Company’s August 2011 equity financing. In accordance with ASC 815-40, the warrant liability are marked to market each quarter-end until they are completely settled. The warrants are valued using the Black-Scholes method, using assumptions consistent with the Company’s application of ASC 505-50. The change in the fair value of the liabilities classified in Level III is due to the unrealized gain of $0.6 million recognized and the gain is presented in the Condensed Statement of Operations (see Note 6).
 
The Company considers carrying amounts of accounts receivable, accounts payable and accrued expenses to approximate fair value due to the short-term nature of these financial instruments.  
 
The Company’s non-financial assets are measured at fair value when there is an indicator of impairment and recorded at fair value only when an impairment charge is recognized.  The Company’s non-financial assets were not material at June 30, 2015 or 2014.
XML 41 R14.htm IDEA: XBRL DOCUMENT v3.2.0.727
Liquidity and Capital Resources
6 Months Ended
Jun. 30, 2015
Liquidity and Capital Resources [Abstract]  
Liquidity and Capital Resources
9.           Liquidity and Capital Resources
 
At June 30, 2015, the Company had cash and cash equivalents of approximately $38.8 million and short-term investments of approximately $15.0 million.  Management believes that the Company’s current cash and cash equivalents and short-term investments, along with the $26.8 million of net proceeds received from our underwritten public offering on July 21, 2015 (see Note 13), will be sufficient to fund its operations for the foreseeable future.  The estimate is based, in part, upon the Company’s currently projected expenditures for the remainder of 2015 and the first six months of 2016 of approximately $53.1 million, which includes approximately $36.1 million for its clinical programs for aldoxorubicin, approximately $2.3 million for pre-clinical development of new albumin-binding cancer drug candidates, approximately $3.9 million for general operation of its clinical programs, and approximately $10.8 million for other general and administrative expenses (including pre-commercialization). These projected expenditures are also based upon numerous other assumptions and subject to many uncertainties, and the Company’s actual expenditures may be significantly different from these projections.
 
If the Company obtains marketing approval and successfully commercializes aldoxorubicin or other product candidates, the Company anticipates it could take several years, for it to generate significant recurring revenue.  The Company will be dependent on future financing and possible strategic partnerships until such time, if ever, as it can generate significant recurring revenue. The Company has no commitments from third parties to provide any additional financing, and it may not be able to obtain future financing on favorable terms, or at all. If the Company fails to obtain sufficient funding when needed, it may be forced to delay, scale back or eliminate all or a portion of its development programs or clinical trials, seek to license to other companies its product candidates or technologies that it would prefer to develop and commercialize itself, or seek to sell some or all of its assets or merge with or be acquired by another company.
XML 42 R16.htm IDEA: XBRL DOCUMENT v3.2.0.727
Income Taxes
6 Months Ended
Jun. 30, 2015
Income Taxes [Abstract]  
Income Taxes
11.           Income Taxes
 
At December 31, 2014, the Company had federal and state net operating loss carryforwards as of  $227.5 million and $157.5 million, respectively, available to offset against future taxable income, and which expire in 2015 through 2034. Of such loss carryforwards, $165.2 million and $157.5 million, respectively, are not subject to limitation under Section 382 of the Internal Revenue Code.
XML 43 R34.htm IDEA: XBRL DOCUMENT v3.2.0.727
Subsequent Events (Details) - USD ($)
6 Months Ended
Jul. 24, 2015
Feb. 05, 2014
Jun. 30, 2015
Jun. 30, 2014
Jul. 31, 2015
Dec. 31, 2014
Dec. 31, 2013
Subsequent Event [Line Items]              
Stock issued, underwritten public offering, value   $ 86,000,000          
Stock issued underwritten public offering (in shares)   13,200,000          
Share price (in dollars per share)   $ 6.50          
Proceeds, exclusive of treasury shares     $ 0 $ 80,535,401      
Current assets:              
Cash and cash equivalents     38,833,736 $ 51,866,891   $ 32,218,905 $ 11,483,112
Short-term investments     15,002,213     45,621,593  
Prepaid and other current assets     976,325     3,250,355  
Total current assets     60,001,477     83,214,773  
Total assets     62,633,809     85,692,582  
LIABILITIES AND STOCKHOLDERS' EQUITY              
Warrant liability     4,566,515   $ 0 5,131,085  
Total current liabilities     20,271,281     17,781,119  
Stockholders' equity              
Common stock     55,927     55,924  
Additional paid-in capital     380,638,689     376,975,984  
Treasury stock     (2,612,861)     (2,612,861)  
Accumulated deficit     (335,719,227)     (306,507,584)  
Total stockholders' equity     42,362,528     67,911,463  
Total liabilities and stockholders' equity     62,633,809     85,692,582  
Warrant liability     4,566,515   0 $ 5,131,085  
Actual [Member]              
Current assets:              
Cash and cash equivalents     38,833,736        
Short-term investments     15,002,213        
Prepaid and other current assets     6,165,528        
Total current assets     60,001,477        
Non-current assets     2,632,332        
Total assets     62,633,809        
LIABILITIES AND STOCKHOLDERS' EQUITY              
Accounts payable and other current liabilities     15,704,766        
Total current liabilities     20,271,281        
Stockholders' equity              
Common stock     55,927        
Additional paid-in capital     380,638,689        
Treasury stock     (2,612,861)        
Accumulated deficit     (335,719,227)        
Total stockholders' equity     42,362,528        
Total liabilities and stockholders' equity     62,633,809        
Pro Forma [Member]              
Current assets:              
Cash and cash equivalents     65,585,761        
Short-term investments     15,002,213        
Prepaid and other current assets     6,431,491        
Total current assets     87,019,465        
Non-current assets     2,632,332        
Total assets     89,651,797        
LIABILITIES AND STOCKHOLDERS' EQUITY              
Accounts payable and other current liabilities     15,704,766        
Total current liabilities     20,271,281        
Stockholders' equity              
Common stock     66,392        
Additional paid-in capital     407,380,249        
Treasury stock     (2,612,861)        
Accumulated deficit     (335,719,227)        
Total stockholders' equity     69,114,553        
Total liabilities and stockholders' equity     $ 89,385,834        
Subsequent Event [Member] | IPO [Member]              
Subsequent Event [Line Items]              
Stock issued, underwritten public offering, value $ 28,700,000            
Stock issued underwritten public offering (in shares) 10,465,000            
Share price (in dollars per share) $ 2.75            
Proceeds, exclusive of treasury shares $ 26,800,000            
Subsequent Event [Member] | Adjustment [Member]              
Current assets:              
Cash and cash equivalents         26,752,025    
Short-term investments         0    
Prepaid and other current assets         0    
Total current assets         26,752,025    
Non-current assets         0    
Total assets         26,752,025    
LIABILITIES AND STOCKHOLDERS' EQUITY              
Accounts payable and other current liabilities         0    
Total current liabilities         0    
Stockholders' equity              
Common stock         10,465    
Additional paid-in capital         26,741,560    
Treasury stock         0    
Accumulated deficit         0    
Total stockholders' equity         26,752,025    
Total liabilities and stockholders' equity         $ 26,752,025    
XML 44 R21.htm IDEA: XBRL DOCUMENT v3.2.0.727
Fair Value Measurements (Tables)
6 Months Ended
Jun. 30, 2015
Fair Value Measurements [Abstract]  
Fair value measurements by level for assets and liabilities measured at fair value on a recurring basis
The following table summarizes fair value measurements by level at June 30, 2015 for assets and liabilities measured at fair value on a recurring basis:
 
(In thousands)
 
Level I
  
Level II
  
Level III
  
Total
 
Cash equivalents
 $38,437  $  $  $38,437 
Short-term investments
  15,002         15,002 
Warrant liabilities
        (4,567)  (4,567)

The following table summarizes fair value measurements by level at December 31, 2014 for assets and liabilities measured at fair value on a recurring basis:
 
(In thousands)
 
Level I
  
Level II
  
Level III
  
Total
 
Cash equivalents
 $31,159  $  $  $31,159 
Short-term investments
  45,622         45,622 
Warrant liability
        (5,131)  (5,131)
XML 45 R26.htm IDEA: XBRL DOCUMENT v3.2.0.727
Basic and Diluted Net Loss Per Common Share (Details) - shares
shares in Millions
3 Months Ended 6 Months Ended
Jun. 30, 2015
Jun. 30, 2014
Jun. 30, 2015
Jun. 30, 2014
Basic and Diluted Net Loss Per Common Share [Abstract]        
Antidilutive securities excluded from computation of earnings per share, amount (in shares) 17.8 14.6 17.8 14.6
XML 46 R5.htm IDEA: XBRL DOCUMENT v3.2.0.727
CONDENSED STATEMENTS OF CASH FLOWS (Unaudited) - USD ($)
6 Months Ended
Jun. 30, 2015
Jun. 30, 2014
Cash flows from operating activities:    
Net loss $ (29,211,643) $ (11,054,955)
Adjustments to reconcile net loss to net cash used in operating activities:    
Depreciation and amortization 165,830 64,856
Stock-based compensation expense 3,662,708 2,627,010
Fair value adjustment on warrant liability (564,570) (12,234,301)
Net foreign exchange loss 0 (64)
Changes in assets and liabilities:    
Receivables (3,155,714) (1,480,067)
Interest receivable 90,431 (48,929)
Prepaid expenses and other current assets 2,027,993 1,410,893
Accounts payable (1,332,633) (160,032)
Accrued expenses and other current liabilities 4,382,343 3,832,235
Net cash used in operating activities (23,935,255) (17,043,354)
Cash flows from investing activities:    
Purchase of short-term investments (17,960,256) (45,601,506)
Proceeds from the sale of short-term investments 48,579,636 22,084,980
Purchases of equipment and furnishings (69,294) (20,733)
Net cash provided by (used in) investing activities 30,550,086 (23,537,259)
Cash flows from financing activities:    
Net proceeds from public offering 0 80,535,401
Proceeds from issuance of restricted stock to employee 0 100
Net proceeds from exercise of warrants and stock options 0 428,891
Net cash provided by financing activities 0 80,964,392
Net increase in cash and cash equivalents 6,614,831 40,383,779
Cash and cash equivalents at beginning of period 32,218,905 11,483,112
Cash and cash equivalents at end of period 38,833,736 51,866,891
Supplemental disclosure of cash flow information:    
Equipment and furnishings purchased on credit 5,022 107,506
Cashless warrant exercises 3 133
Cash paid for income taxes $ 800 $ 59,431
XML 47 R10.htm IDEA: XBRL DOCUMENT v3.2.0.727
Basic and Diluted Net Loss Per Common Share
6 Months Ended
Jun. 30, 2015
Basic and Diluted Net Loss Per Common Share [Abstract]  
Basic and Diluted Net Loss Per Common Share
5.           Basic and Diluted Net Loss Per Common Share
 
Basic and diluted net loss per common share is computed based on the weighted-average number of common shares outstanding. Common share equivalents (which consist of options, warrants and restricted stock) are excluded from the computation of diluted net loss per common share where the effect would be anti-dilutive.  Common share equivalents that could potentially dilute net loss per share in the future, and which were excluded from the computation of diluted loss per share, totaled 17.8 million shares for each of the three-month and six-month periods ended June 30, 2015, and 14.6 million shares for each of the three-month and six-month periods ended June 30, 2014.
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Warrant Liabilities (Details) - USD ($)
3 Months Ended 6 Months Ended
Jun. 30, 2015
Jun. 30, 2014
Jun. 30, 2015
Jun. 30, 2014
Derivative [Line Items]        
Gain (loss) on warrant liability $ 2,435,865 $ (2,468,603) $ 564,570 $ 12,234,301
Warrants [Member]        
Derivative [Line Items]        
Risk-free interest rate (in hundredths)     0.28% 0.44%
Expected dividend yield (in hundredths)     0.00% 0.00%
Expected lives     1 year 1 month 2 days 1 year 11 months 16 days
Expected volatility (in hundredths)     62.70% 84.10%
Warrants classified as liabilities (in shares) 6,371,854 6,984,716 6,371,854 6,984,716
Gain (loss) on warrant liability $ 2,435,865 $ (2,468,603) $ 564,570 $ 12,234,301
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Stock Based Compensation (Tables)
6 Months Ended
Jun. 30, 2015
Stock Based Compensation [Abstract]  
Schedule of total stock-based compensation expense from stock options and warrants
The following table sets forth the total stock-based compensation expense resulting from stock options and warrants included in the Company’s unaudited interim statements of operations:
 
   
Three Months Ended June 30,
  
Six Months Ended June 30,
 
   
2015
  
2014
  
2015
  
2014
 
Research and development — employee
 $392,842  $234,484  $728,780  $409,638 
General and administrative — employee
  1,744,440   325,379   2,699,844   637,339 
Total employee stock-based compensation
 $2,137,282  $559,863  $3,428,624  $1,046,977 
                  
Research and development — non-employee
 $  $  $  $ 
General and administrative — non-employee
  140,533   160,629   234,084   352,620 
 Total non-employee stock-based compensation
 $140,533  $160,629  $234,084  $352,620 
Schedule of share-based payment award, fair value of the stock options granted , assumptions
The fair value of the stock options was estimated using the Black-Scholes option-pricing model, based on the following assumptions:
 
 
 
Six Months Ended June 30, 2015
  
Six Months Ended June 30, 2014
 
Risk-free interest rate
  2.21%  1.92%
Expected volatility
  78.2% - 84.4%  87.0% - 89.6%
Expected lives (years)
  6 - 10   6 - 10 
Expected dividend yield
  0.00%  0.00%
Schedule of share-based compensation, stock options, activity
Presented below is the Company’s stock option activity:
 
 
 
Six Months Ended June 30, 2015
 
 
 
 
Number of Options (Employees)
  
Number of Options (Non-Employees)
  
Total Number
of Options
  
Weighted-Average Exercise Price
 
Outstanding at January 1, 2015
  9,348,952   692,143   10,040,735  $2.87 
Granted
  550,000      550,000  $3.86 
Expired
  (68,000)  (56,429)  (124,429) $6.90 
Outstanding at June 30, 2015
  9,830,952   635,714   10,466,306  $3.33 
Options exercisable at June 30, 2015
  6,276,275   635,714   6,911,989  $3.59 
Schedule of share-based compensation, summarizes significant ranges of outstanding stock options
The following table summarizes significant ranges of outstanding stock options under the Company’s plans at June 30, 2015:

Range of
 Exercise Prices
  
Total Number
of Options
  
Weighted-Average Remaining Contractual Life (years)
  
Weighted-Average Exercise Price
  
Total Number of Options Exercisable
  
Weighted-Average Remaining Contractual Life (years)
  
Weighted-Average Exercise Price
 
$1.83 - $2.50   5,837,558   8.51  $2.12   3,226,398   8.00  $2.08 
$2.51 – $3.50   954,482   8.64  $2.85   874,482   8.62  $2.83 
$3.51 – $8.00   3,386,201   7.93  $5.06   2,523,043   7.74  $5.16 
$8.01 – $32.55   288,065   2.31  $9.00   288,066   2.31  $9.00 
     10,466,306   8.16  $3.33   6,911,989   7.74  $3.59