0000799698-17-000023.txt : 20170803 0000799698-17-000023.hdr.sgml : 20170803 20170802205043 ACCESSION NUMBER: 0000799698-17-000023 CONFORMED SUBMISSION TYPE: 10-Q PUBLIC DOCUMENT COUNT: 52 CONFORMED PERIOD OF REPORT: 20170630 FILED AS OF DATE: 20170803 DATE AS OF CHANGE: 20170802 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: 171001875 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 form10q-2q17.htm QUARTERLY REPORT FOR QUARTER ENDING JUNE 30, 2017 ON FORM 10-Q



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, 2017

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, smaller reporting company, or an emerging growth company. See the definitions of "large accelerated filer," "accelerated filer," "smaller reporting company," and "emerging growth company" in Rule 12b-2 of the Exchange Act:
Large accelerated filer £
Accelerated filer R
Non-accelerated filer £
(Do not check if a smaller reporting company)
 
Smaller reporting company £
 
Emerging growth company  £
If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. £
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, $0.001 par value, outstanding as of August 3, 2017: 165,710,526 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
 19
   
PART II. — OTHER INFORMATION
 
Item 1. Legal Proceedings
 20
Item 6. Exhibits
 20
   
SIGNATURES
 21
   
INDEX TO EXHIBITS
 22



PART I — FINANCIAL INFORMATION
Item 1. — Financial Statements
CYTRX CORPORATION
CONDENSED BALANCE SHEETS
(Unaudited)
   
June 30,
2017
   
December 31,
2016
 
ASSETS
           
Current assets:
           
Cash and cash equivalents
 
$
54,972,846
   
$
56,959,485
 
Receivables
   
47,631
     
183,703
 
Prepaid expenses and other current assets
   
1,782,141
     
3,434,238
 
Total current assets
   
56,802,618
     
60,577,426
 
Equipment and furnishings, net
   
1,323,579
     
1,959,667
 
Goodwill
   
183,780
     
183,780
 
Other assets
   
38,014
     
48,911
 
Total assets
 
$
58,347,991
   
$
62,769,784
 
LIABILITIES AND STOCKHOLDERS' EQUITY
               
                 
Current liabilities:
Accounts payable
 
$
7,080,080
   
$
6,406,445
 
Accrued expenses and other current liabilities
   
2,972,082
     
3,830,498
 
Warrant liabilities
   
6,567,080
     
3,789,391
 
Term loan, net - current
   
6,701,040
     
5,481,656
 
Total current liabilities
   
23,320,282
     
19,507,990
 
                 
Long term loan, net
   
15,813,507
     
18,484,510
 
     Total liabilities
   
39,133,789
     
37,992,500
 
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
   
     
 
Preferred Stock, $1,000 stated value, 3,900 shares authorized, 0 and 3,108 outstanding at June 30, 2017 and December 31, 2016
   
     
3,108,000
 
Common stock, $0.001 par value, 250,000,000 shares authorized;  153,127,389 shares issued and outstanding at June 30, 2017; 111,322,895 shares issued and outstanding at December 31, 2016
   
153,126
     
111,321
 
Additional paid-in capital
   
460,329,472
     
437,423,958
 
Accumulated deficit
   
(441,268,396
)
   
(415,865,995
)
Total stockholders' equity
   
19,214,202
     
24,777,284
 
Total liabilities and stockholders' equity
 
$
58,347,991
   
$
62,769,784
 

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,
 
   
2017
   
2016
   
2017
   
2016
 
Revenue:
                       
License revenue
 
$
   
$
100,000
   
$
   
$
100,000
 
                                 
Expenses:
                               
Research and development
   
6,167,074
     
12,452,340
     
12,934,058
     
20,604,559
 
General and administrative
   
3,137,008
     
6,128,904
     
6,116,063
     
10,087,340
 
     
9,304,082
     
18,581,244
     
19,050,121
     
30,691,899
 
                                 
Loss before other income (loss)
   
(9,304,082
)
   
(18,481,244
)
   
(19,050,121
)
   
(30,591,899
)
                                 
Other income (loss):
                               
Interest income
   
90,849
     
65,436
     
151,392
     
127,174
 
Interest expense
   
(848,395
)
   
(741,346
)
   
(2,171,110
)
   
(1,158,148
)
Other income (loss), net
   
7,276
     
(798
)
   
3,504
     
6,081
 
Gain (loss) on warrant derivative liabilities
   
(4,303,945
)
   
877,729
     
(4,336,066
)
   
693,457
 
                                 
Net loss
 
$
(14,358,297
)
 
$
(18,280,223
)
 
$
(25,402,401
)
 
$
(30,923,335
)
                                 
Basic and diluted net loss per share
 
$
(0.10
)
 
$
(0.27
)
 
$
(0.20
)
 
$
(0.46
)
                                 
Basic and diluted weighted-average shares outstanding
   
139,070,329
     
67,398,837
     
126,394,244
     
66,893,846
 
                                 
                                 

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,
 
   
2017
   
2016
 
Cash flows from operating activities:
           
Net loss
 
$
(25,402,401
)
 
$
(30,923,335
)
Adjustments to reconcile net loss to net cash used in operating activities:
               
Depreciation and amortization
   
348,843
     
213,964
 
Stock-based compensation expense
   
1,731,484
     
4,364,886
 
Fair value adjustment on warrant liabilities
   
4,336,066
     
(693,457
)
Non-cash litigation settlement due in common stock
   
     
700,000
 
Amortization of loan cost and discount
   
975,743
     
208,148
 
Loss on retirement of fixed assets
   
421,843
     
3,388
 
Changes in assets and liabilities:
               
Receivables
   
136,072
     
4,368,773
 
Interest receivable
   
     
28,130
 
Prepaid expenses and other current assets
   
1,662,994
     
1,432,127
 
Accounts payable
   
673,635
     
(844,373
)
Accrued expenses and other current liabilities
   
(1,026,781
)
   
(4,297,864
)
Net cash used in operating activities
   
(16,142,502
)
   
(25,439,613
)
                 
Cash flows from investing activities:
               
 Proceeds from the sale of short-term investments
   
     
35,035,420
 
 Purchases of equipment and furnishings
   
(134,598
)
   
(660,758
)
Net cash provided by (used in) investing activities
   
(134,598
)
   
34,374,662
 
                 
Cash flows from financing activities:
               
Proceeds from public offering
   
13,951,218
     
 
Proceeds from term loan, net
   
     
24,012,078
 
Payment of principal on term loan
   
(2,427,362
)
   
 
Net proceeds from exercise of warrants and stock options
   
2,766,605
     
704,700
 
Net cash provided by financing activities
   
14,290,461
     
24,716,778
 
                 
Net increase (decrease) in cash and cash equivalents
   
(1,986,639
)
   
33,651,827
 
Cash and cash equivalents at beginning of period
   
56,959,485
     
22,261,372
 
Cash and cash equivalents at end of period
 
$
54,972,846
   
$
55,913,199
 
                 
Supplemental disclosure of cash flow information:
               
                 
Cash paid during the year for interest
 
$
1,212,219
   
$
752,083
 
                 
Cash paid for income taxes
 
$
800
   
$
800
 

Supplemental disclosure of non-cash activties:
           
             
Warrant liability exercise
 
$
1,558,377
   
$
 
                 
Preferred stock conversion
 
$
7,400
   
$
 
                 
Warrants issued in connection with term loan
 
$
   
$
633,749
 
                 
Equipment and furnishings purchased on credit
 
$
   
$
79,247
 
                 
Shares issued in connection with the class action settlement
 
$
   
$
4,500,000
 

The accompanying notes are an integral part of these condensed financial statements.
3

NOTES TO CONDENSED FINANCIAL STATEMENTS
June 30, 2017
(Unaudited)
1.  Description of Company and Basis of Presentation
CytRx Corporation ("we," "us," "our," CytRx" or the "company") is a biopharmaceutical company specializing in oncology.  Our focus is on the discovery, research and clinical development of novel anti-cancer drug candidates that employ linker technologies to enhance the accumulation and release of drug at the tumor.  Aldoxorubicin, our lead clinical candidate, has been tested in over 600 patients with various types of cancer.

CytRx's lead product candidate is aldoxorubicin, a conjugate of the commonly prescribed chemotherapeutic agent doxorubicin that binds to circulating albumin in the bloodstream and is believed to concentrate the drug at the site of the tumor.  Specifically, it is comprised of (6-maleimidocaproyl) hydrazine, an acid-sensitive molecule that is conjugated to doxorubicin.  Our lead indication for aldoxorubicin is for patients with advanced soft tissue sarcomas (STS). We met with the FDA in March 2017 to discuss a regulatory pathway for a New Drug Application (NDA) for aldoxorubicin in STS.

Aldoxorubicin has received Orphan Drug Designation (ODD) by the U.S. FDA for the treatment of STS. ODD provides several benefits including seven years of market exclusivity after approval, certain R&D related tax credits, and protocol assistance by the FDA. European regulators granted aldoxorubicin Orphan designation for STS which confers ten years of market exclusivity among other benefits.

On July 27, 2017, CytRx entered into an exclusive worldwide license with NantCell, Inc. ("NantCell"), granting them rights to develop, manufacture and commercialize aldoxorubicin in all indications.  As part of the license, NantCell made a strategic investment of $13 million in CytRx common stock $1.10 per share, a premium of 92% to the market price on that date.  CytRx is entitled to receive up to $343 million in milestones related to regulatory approvals and commercial milestones.  CytRx is entitled to receive ascending double-digit royalties for net sales for soft tissue sarcomas and mid to high single digit royalties for other indications.  NantCell will take over the development, manufacturing and commercialization responsibility for aldoxorubicin including the cost of filing the NDA.

CytRx has an active drug discovery and research operation at our laboratory facilities in Freiburg, Germany, focusing on the creation of novel drug anti-cancer candidates by combining our proprietary linker technologies with ultra-high potency cytotoxic drugs. We are expanding our pipeline of ultra-high potency oncology candidates through our LADR™ (Linker Activated Drug Release) technology platform, a discovery engine designed to leverage CytRx's expertise in albumin biology and next generation linker technologies for the development of a new class of potential breakthrough anti-cancer therapies.

We have created a "toolbox" of linker technologies that have the ability to significantly increase the therapeutic index of ultra-high potency drugs (10-1,000 times more potent than traditional chemotherapies) by controlling the release of the drug payloads and improving drug-like properties. After infusion, these ultra-high potency drug conjugates bind to circulating albumin for transport of the drug to the tumor.  Subsequently, due to specific conditions within the tumor, the linkers are cleaved and release the anti-cancer drug payload.

Our current efforts are focused on two classes of ultra-high potency drug conjugates.  Our strategy across these programs is to generate additional pre-clinical data that will allow us to make informed decisions regarding the selection of one or both programs for moving into human clinical trials either independently or on a partnered basis.

The accompanying condensed financial statements at June 30, 2017 and for the three-month and six-month periods ended June 30, 2017 and 2016, 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, 2016 have been derived from the our audited financial statements as of that date.
The financial statements included herein have been prepared by us 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, 2016.
4

 As a result of the worldwide license of all of our rights to aldoxorubicin to NantCell, NantCell will take over the development, manufacturing and commercialization responsibility for aldoxorubicin, thereby enabling us to eliminate our future research and development activities related to aldoxorubicin. Currently, our only research and development activities are conducted by our Freiburg, Germany, laboratory facility.  For this reason and others, our operating expenses are expected to be significantly lower in the near future. Therefore, period-to-period comparisons should not be relied upon as predictive of the results in future periods.
2. Foreign Currency Remeasurement
The U.S. dollar has been determined to be the functional currency for the net assets of our German laboratory facilty. 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 current 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 $6,200 and $1,300, respectively, for the three-month and six-month periods ended June 30, 2017 and a gain of approximately $600 and $5,800, respectively, for the three and six-month periods ended June 30, 2016, respectively. The Company does not engage in currency hedging transactions.
3. Recent Accounting Pronouncements
In January 2017, the FASB issued updated guidance to clarify the definition of a business within the context of business combinations. The updated guidance requires that when substantially all of the fair value of the gross assets acquired (or disposed of) is concentrated in a single identifiable asset or a group of similar identifiable assets, the set is not a business. This updated guidance is expected to reduce the number of transactions that need to be further evaluated as business combinations. If further evaluation is necessary, the updated guidance will require that a business set include, at a minimum, an input and a substantive process that together significantly contribute to the ability to create output. The updated guidance will remove the evaluation of whether a market participant could replace missing elements. The new guidance is effective for annual and interim periods beginning after December 15, 2017 and is to be applied on a prospective basis. We are currently evaluating the new guidance.

In January 2017, the FASB issued updated guidance which eliminated Step 2 from the goodwill impairment test. Step 2 is the process of measuring a goodwill impairment loss by comparing the implied fair value of a reporting unit's goodwill with the carrying amount of that goodwill. The new guidance requires entities to measure a goodwill impairment loss as the amount by which a reporting unit's carrying value exceeds its fair value, limited to the carrying amount of goodwill. The FASB also eliminated the requirements for entities that have reporting units with zero or negative carrying amounts to perform a qualitiative assessment for the goodwill impairment test. Instead, those entities would be required to disclose the amount of goodwill allocated to each reporting unit with a zero or negative carrying amount. The new guidance is effective for intrerim or annual goodwill impairment tests performed in fiscal years beginning after December 15, 2019, with early adoption permitted. We are currently evaluating the new guidance.

In March 2016, the FASB issued Accounting Standards Update 2016-09, Compensation—Stock Compensation ("ASU 2016-09"). ASU 2016-09 includes several areas of simplification to stock compensation including simplifications to the accounting for income taxes, classification of excess tax benefits on the Statement of Cash Flows and forfeitures. ASU 2016-09 is effective for annual reporting periods beginning after December 15, 2016. We adopted this Standard on January 1, 2017. The adoption of this Standard did not have material impact to the Company's financial position or its results of operations.
In February 2016, the FASB issued Accounting Standards Update 2016-02, Leases ("ASU 2016-02"). ASU 2016-02 allows the recognition of lease assets and lease liabilities by lessees for those leases classified as operating leases under previous GAAP. The classification criteria for distinguishing between finance leases and operating leases are substantially similar to the classification criteria for distinguishing between capital leases and operating leases in the previous leases guidance. The Update 2016-02 is effective for annual reporting periods beginning after December 15, 2018 and early adoption is permitted. We are still evaluating the effect of this update.
In January 2016, the FASB issued Accounting Standards Update 2016-01, Recognition and Measurement of Financial Assets and Financial Liabilities ("ASU 2016-01"). ASU 2016-01 eliminates the requirement to disclose the methods and significant assumptions used to estimate the fair value that is required to be disclosed for financial instruments measured at amortized cost on the balance sheet. The standard also clarifies the need to evaluate a valuation allowance on a deferred tax asset related to available-for-sale securities in combination with our other deferred tax assets. The update 2016-01 is effective for annual reporting periods beginning after December 15, 2017. The adoption of this standard is not expected to have a material impact on our financial statements.
5


4. Term Loan
On February 5, 2016, we entered into a loan and security agreement with Hercules Technology Growth Capital, Inc. ("HTGC"), as administrative agent and lender, and Hercules Technology III, L.P., as lender ("Hercules"), pursuant to which the lenders made term loans to us on February 8, 2016 in the aggregate principal amount of $25 million (the "Term Loans"). 
The Term Loans bear interest at the daily variable rate per annum equal to 6.0% plus the prime rate, or 10.25%, whichever is greater.  We are required to make interest-only payments on the Term Loans through February 28, 2017, and beginning on March 1, 2017 blended equal monthly installments of principal amortization and accrued interest until the maturity date of the Term Loans on February 1, 2020.  Under the terms of the loan, we are required to maintain a minimum cash balance equal to the greater of (i) $10 million or (ii) forward three months projected cash burn. As security under our obligations, we issued to the lenders warrants to purchase a total of 634,146 shares of our common stock at an exercise price of $2.05. These warrants are classified as equity warrants with a fair value of $633,749.  All outstanding principal and accrued interest on the term loans will be due and payable in full on the maturity date of February 1, 2020.
As security for our obligations under the loan and securities agreement, we granted HTGC, as administrative agent, a security interest in substantially all of our existing and after-acquired assets except for our intellectual property and certain other excluded assets. The loan and security agreement contains customary representations, warranties and covenants.
   
June 30,
2017
   
December 31,
2016
 
Term Loan Principal – Current
 
$
7,737,492
   
$
6,214,057
 
Issuance Cost/Loan Discount – Current
   
(1,036,452
)
   
(732,401
)
Term Loan, Net – Current
 
$
6,701,040
   
$
5,481,656
 
                 
Long Term Loan Principal
 
$
14,835,146
   
$
18,785,943
 
End Fee Payable
   
1,771,250
     
1,771,250
 
Long Term Loan Discount/Issuance Cost
   
(792,889
)
   
(2,072,683
)
Long Term Loan, Net
 
$
15,813,507
   
$
18,484,510
 

On July 28, 2017, we entererd into an Amended Loan Services Agreement with the lenders of the Term Loans whereby we agreed to make an immediate payment of $5 million of principal and unpaid interest, a further $5 million payment of principal and unpaid interest by September 30, 2017, and agreed to an updated schedule of monthly payments and a new maturity date of August 1, 2018.
The interest expense on the loan for the three-month and six-month periods ended June 30, 2017 was $848,395 and $2,171,110, respectively, as compared to $741,346 and $1,158,148 for comparative 2016 periods.
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 and warrants) 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 44.8 million shares for each of the three-month and six-month periods ended June 30, 2017, and 22.4 million shares for each of the three-month and six-month periods ended June 30, 2016.
6

6. Warrant Liabilities
Liabilities measured at fair value on a recurring basis include warrant liabilities resulting from our equity financings.  In accordance with ASC 815-40, Derivatives and Hedging – Contracts in Entity's Own Equity ("ASC 815-40"), the warrant liabilities are 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. We recognized a loss of $4.3 million and a gain of $0.9 million for the three-month periods ended June 30, 2017 and 2016, respectively, and a loss of $4.3 million and a gain of $0.7 million for the six-month periods ended June 30, 2017 and 2016, respectively. The following reflects the weighted-average assumptions for each of the six-month periods indicated:
   
Six Months Ended June 30,
 
   
2017
   
2016
 
             
Risk-free interest rate
   
1.13
%
   
0.20
%
Expected dividend yield
   
0
%
   
0
%
Expected lives
   
0.79
     
0.09
 
  Expected volatility
   
125.3
%
   
59.3
%
  Warrants classified as liabilities (in shares)
   
24,110,577
     
6,371,854
 
                 
Our computation of expected volatility is based on the historical daily volatility of our publicly traded stock. The dividend yield assumption of zero is based upon the fact that we have never paid cash dividends and presently have 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.
On July 19, 2017, 6,340,148 warrants expired.
7. Stock Based Compensation
We have a 2000 Long-Term Incentive Plan, which expired on August 6, 2010.  As of June 30, 2017, there were approximately 0.4 million shares subject to outstanding stock options under this plan.  No further shares are available for future grant under this plan.
We also have a 2008 Stock Incentive Plan.  As of June 30, 2017, there were 16.4 million shares subject to outstanding stock options and 2.5 million shares outstanding related to restricted stock grants options and 10.4 million shares available for future grant under this plan.
We follow 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, we recognize 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 our Condensed Statements of Operations:
7

   
Three Months Ended June 30,
   
Six Months Ended June 30,
 
   
2017
   
2016
   
2017
   
2016
 
Research and development — employee
 
$
278,533
   
$
507,195
   
$
631,616
   
$
988,006
 
General and administrative — employee
   
401,820
     
2,499,368
     
869,485
     
3,156,418
 
Total employee stock-based compensation
 
$
680,353
   
$
3,006,563
   
$
1,501,101
   
$
4,144,424
 
                                 
Research and development — non-employee
 
$
   
$
   
$
   
$
 
General and administrative — non-employee
   
36,578
     
32,506
     
65,237
     
220,462
 
Total non-employee stock-based compensation
 
$
36,578
   
$
32,506
   
$
65,237
   
$
220,462
 

During the six-month period ended June 30, 2017, we granted stock options to purchase 10,000 shares of our common stock at an average weighted exercise price of $0.41. During the six-month period ended June 30, 2016, we granted stock options to purchase 425,000 shares of our common stock and warrants to purchase 500,000 shares of our common stock at a weighted average exercise price of $1.74. In the three-month period ended June 30, 2016, we amended the terms of stock options of a former executive in respect of a Retirement Agreement, resulting in a one-time expense of approximately $1.9 million. 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, 2017
   
Six Months Ended June 30, 2016
 
Risk-free interest rate
   
2.04
%
   
1.47
%
Expected volatility
   
85.5
%
   
76.3
%
Expected lives (years)
   
6
     
5 - 10
 
Expected dividend yield
   
0.00
%
   
0.00
%
 
Our computation of expected volatility is based on the historical daily volatility of our publicly traded stock.  We use historical information to compute expected lives. In the six-month period ended June 30, 2017, the contractual term of the options granted was ten years. The dividend yield assumption of zero is based upon the fact we have never paid cash dividends and presently have 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, 2016, we estimated annualized forfeiture rates of 10% for options granted to our 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  Compensation costs will be adjusted for future changes in estimated forfeitures.  We 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. On January 1, 2017, we adopted ASU 2016-09 and made a policy election to recognize forfeitures as they occur. The adoption of ASU 2016-09 did not have a material impact to the Company's financial condition or results of operations. No amounts relating to stock-based compensation have been capitalized.
As of June 30, 2017, there remained approximately $2.4 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 1.01 years. Presented below is our stock option activity:
   
Six Months Ended June 30, 2017
 
   
Number of Options (Employees)
   
Number of Options (Non-Employees)
   
Total Number of Options
   
Weighted-Average Exercise Price
 
Outstanding at January 1, 2017
   
16,879,770
     
600,000
     
17,479,770
   
$
2.37
 
Granted
   
10,000
     
     
10,000
   
$
0.41
 
Exercised, Forfeited or Expired
   
(646,847
)
   
     
(646,847
)
 
$
3.16
 
Outstanding at June 30, 2017
   
16,242,923
     
600,000
     
16,842,932
   
$
2.34
 
Options exercisable at June 30, 2017
   
11,655,168
     
600,000
     
12,255,168
   
$
2.75
 

8


The following table summarizes significant ranges of outstanding stock options under our plans at June 30, 2017:

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
 
$
0.41 - $1.50
     
4,317,533
     
9.45
   
$
0.44
     
1,586,461
     
9.46
   
$
0.44
 
$
1.51 – $2.50
     
8,669,296
     
7.32
   
$
2.26
     
6,835,946
     
7.07
   
$
2.22
 
$
2.51 – $4.00
     
960,670
     
6.64
   
$
2.88
     
937,337
     
6.61
   
$
2.87
 
$
4.01 – $32.55
     
2,895,424
     
5.69
   
$
5.24
     
2,895,424
     
5.69
   
$
5.24
 
         
16,842,923
     
7.55
   
$
2.34
     
12,255,168
     
7.02
   
$
2.75
 

The aggregate intrinsic value of all outstanding options and vested options as of June 30, 2017 was $0.8 million and $0.3 million, respectively, representing options with exercise prices of less than the closing fair market value of our common stock on June 30, 2017 of $0.63 per share.
There were 27,989,723 and 32,502,790 warrants outstanding at June 30, 2017 and December 31, 2016, respectively both at a weighted-average exercise price of $0.68.
Restricted Stock
In December 2016, the Company granted to our Chairman and Chief Executive Officer, 2,325,581 shares of restricted common stock, pursuant to the 2008 Plan. This restricted stock vests in equal annual instalments over three years.  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 stock on the grant date was $1,000,000. The Company recorded an employee stock-based compensation expense for restricted stock of approximately $83,029 and $165,146 respectively, for the three and six-month periods ended June 30, 2017 as compared to zero for the comparative 2016 periods.
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, 2017 for assets and liabilities measured at fair value on a recurring basis:
(In thousands)
 
Level I
   
Level II
   
Level III
   
Total
 
Cash equivalents
 
$
53,485
   
$
   
$
   
$
53,485
 
Warrant liabilities
   
     
     
(6,567
)
   
(6,567
)

9

The following table summarizes fair value measurements by level at December 31, 2016 for assets and liabilities measured at fair value on a recurring basis:
(In thousands)
 
Level I
   
Level II
   
Level III
   
Total
 
Cash equivalents
 
$
56,276
   
$
   
$
   
$
56,276
 
Warrant liabilities
   
     
     
(3,789
)
   
(3,789
)

Liabilities measured at market value on a recurring basis include warrant liabilities resulting from recent debt and equity financings. In accordance with ASC 815-40, the warrant liabilities 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 our application of ASC 505-50. The $2.8 million increase in fair value of the warrant liabilities is due to the significant excess of the exercise price over the Company's stock price as of June 30, 2017 and the close proximity to the expiration date of the warrants (see Note 6).
We consider carrying amounts of accounts receivable, accounts payable and accrued expenses to approximate fair value due to the short-term nature of these financial instruments.  
Our 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.  Our non-financial assets were not material at June 30, 2017 or 2016.
9. Liquidity and Capital Resources
At June 30, 2017, we had cash and cash equivalents of approximately $55.0 million.  On July 27, 2017, we entered into a global strategic licensing agreement with NantCell Inc ("NantCell") for the exclusive rights to develop, manufacture and commercialize aldoxorbuicin for all indications. Under the terms of this Agreement, NantCell made a strategic investment into our Company by purchasing $13 million of our common stock. Concurrently, we announced the signing of an amendment to the Loan Services Agreement with Hercules whereby we made an immediate principal repayment of $5 million, a further $5 million repayment by September 30, 2017, and an updated schedule of monthly instalments with a new Term Loan maturity date of August 1, 2018. Under the NantCell license, NantCell agreed to assume all future costs of developing and commercializing aldoxorubicin. Management believes that our current cash and cash equivalents, along with the net proceeds of the common stock purchase (See Note 13), 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 2017 and the first seven months of 2018 of approximately $35.6 million, which includes approximately $4.7 million for our clinical programs for aldoxorubicin, approximately $3.7 million for the research and clinical development of novel anti-cancer drug candidates at our Freiburg operations, approximately $1.1 million for general operation of our clinical programs, approximately $9.4 million for other general and administrative expenses, and approximately $16.6 million for interest and payments on the term loan. 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 our licensing partner obtains marketing approval and successfully commercializes aldoxorubicin, we anticipate it could take several years, for it to generate significant recurring revenue.  We will be dependent on future financing and possible other strategic partnerships until such time, if ever, as it can generate significant recurring revenue. We have no commitments from third parties to provide 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, seek to license to other companies our product candidates or technologies that we would prefer to develop and commercialize ourself, or seek to sell some or all of our assets or merge with or be acquired by another company.
10. Equity Transactions
In the first quarter of 2017, there were 3,108 shares of our outstanding Series B Convertible Preferred converted by the holders into 7.4 million shares of our common stock.
In the second quarter of 2017, there were 4,404,494 shares of our common stock issued from the exercise of warrants.
On May 2, 2017, we issued 30.0 million shares of our common stock in a public offering.
As of June 30, 2017, we have reserved approximately 10.4 million of our authorized but unissued shares of common stock for future issuance pursuant to our employee stock option plans issued to employees and consultants.

11. Income Taxes
At December 31, 2016, we had federal and state net operating loss carryforwards as of  $339.0 million and $224.0 million, respectively, available to offset against future taxable income, which expire in 2017 through 2036, of which $152.0 million and $145.0 million, respectively, are not subject to limitation under Section 382 of the Internal Revenue Code.
10

12. Commitments and contingencies
Commitments
We have an agreement with KTB Tumorforschungs GmbH, or KTB, for the Company's exclusive license of patent rights held by KTB for the worldwide development and commercialization of aldoxorubicin. Under the agreement, we must make payments to KTB in the aggregate of $6.0 million upon meeting clinical and regulatory milestones up to and including the product's second final marketing approval.  We also have 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 we obtain.
In the event that we must pay a third party in order to exercise our right to the intellectual property under the agreement, we will deduct a percentage of those payments from the royalties due KTB, up to an agreed upon cap. As a result of the NantCell license and the sale of $13 million of our shares to NantCell, we will incur an obligation to pay KTB approximately $0.6 million.
Contingencies
We applied the disclosure provisions of ASC 460, Guarantees ("ASC 460") to our agreements that contain guarantees or indemnities by us. We provide (i) indemnifications of varying scope and size to certain investors and other parties for certain losses suffered or incurred by the indemnified party in connection with various types of third-party claims; and (ii) indemnifications of varying scope and size to officers and directors against third party claims arising from the services they provide to us.
 
Shareholder Derivative Actions in Delaware.  There are two competing derivative complaints pending in the Delaware Court of Chancery alleging claims related to our alleged retention of DreamTeamGroup and MissionIR.  On December 14, 2015, a shareholder derivative complaint, captioned Niedermeyer et al. v. Kriegsman et al., C.A. No. 11800, was filed against certain of our officers and directors, for which a second amended complaint was filed on October 12, 2016.  On September 6, 2016, one of the plaintiffs in the California litigation (discussed above) effectively refiled his complaint in the Delaware Court of Chancery, with the case captioned Taylor v. Kriegsman, C.A. No. 12720.  Following competing motions for appointment of a lead plaintiff and lead counsel, On February 22, 2017, the Court of Chancery appointed Niedermeyer et al.as lead plaintiffs in the complaint. On May 3, 2017, the parties entered into negotiations with a mediator and on June 2, 2017, the parties entered into a Memorandum of Understanding ("MOU") to settle the entire action. On June 15, 2017, the MOU was submitted to the Court.
 
Class Action in California.  On July 25 and 29, 2016, nearly identical class action complaints were filed in the U.S. District Court for the Central District of California, titled Crihfield v. CytRx Corp., et al., Case No. 2:16-cv-05519 and Dorce v. CytRx Corp., Case No. 2:16-cv-05666 alleging that we and certain of our officers violated the Securities Exchange Act of 1934 by allegedly making materially false and/or misleading statements, and/or failing to disclose material adverse facts to the effect that the clinical hold placed on the Phase 3 trial of aldoxorubicin for STS would prevent sufficient follow-up for patients involved in the study, thus requiring further analysis, which could cause the trial's results and/or FDA approval to be materially adversely affected or delayed.  The plaintiffs allege that such wrongful acts and omissions caused significant losses and damages to a class of persons and entities that acquired our securities between November 18, 2014 and July 11, 2016, and seek an award of compensatory damages, costs and expenses, including counsel and expert fees, and such other and further relief as the Court may deem just and proper. On October 26, 2016, the Court entered an Order consolidating the actions titled In re: CytRx Corporation Securities Litigation, Master File No. 16-cv-05519-SJO and appointing a Lead Plaintiff and Lead Counsel. Following the filing of a first amended complaint on January 13, 2017, on March 14, 2017 the Company and the individual defendants filed a Motion to Dismiss.  Plaintiff filed an Opposition thereto on April 28, 2017. The Company and the individual defendants filed a Reply on May 30, 2017 and the matter was heard by the Court on June 12, 2017. On June 14, 2017, the Court issued an Order granting the Motion to Dismiss with leave to amend. Plaintiff filed a Second Amended Complaint and the Individual Defendants filed a renewed Motion to Dismiss. Plaintiff filed an Opposition thereto on July 24, 2017. The Company and the Individual Defendants filed a Reply on July 31, 2017 and the matter is set to be heard by the Court on August 14, 2017.
The Company intends to vigorously defend against the foregoing complaints. CytRx has directors' and officers' liability insurance, which will be utilized in the defense of these matters. 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 management's view of these matters may change in the future.
     11

 
    The Company evaluates developments in legal proceedings and other matters on a quarterly basis. The Company records accruals for loss contingencies to the extent that the Company concludes that it is probable that a liability has been incurred and the amount of the related loss can be reasonably estimated. The Company has accrued $0.7 million of litigation settlement related to Shareholder Derivative actions.

We evaluate developments in legal proceedings and other matters on a quarterly basis. If an unfavorable outcome becomes probable and reasonably estimable, we could incur charges that could have a material adverse impact on our financial condition and results of operations for the period in which the outcome becomes probable and reasonably estimable.
13. Subsequent Events
On July 27, 2017, we entered into a global strategic license agreement (the "License Agreement") with NantCell, Inc. ("NantCell"), for providing NantCell the exclusive rights to develop and commercialize aldoxorubicin for all indications. Under the terms of the License Agreement, CytRx is entitled to receive up to $343 million in milestone payments related to regulatory approvals and commercial milestones for aldoxorubicin. In addition, CytRx will receive certain specified royalties for all other indications (our receipt of which would obligate us to make certain payments to KTB). NantCell will be responsible for all future development, manufacturing and commercialization expenses, other than royalties and milestones that may be owed by CytRx under its existing license agreements.
In connection with the License Agreement, on July 27, 2017, CytRx (i) entered into a stock purchase agreement with NantCell in which NantCell purchased $13 million of CytRx common stock at $1.10 per share, a 92% premium to market on that date, and (ii) issued to NantCell a warrant to purchase up to 3 million shares of common stock at $1.10, expiring on January 27, 2019.
On July 27, 2017, we entered into a First Amendment to Loan and Security Agreement with Hercules  to amend our existing long-term loan facility (the "Loan Agreement") originally entered into on February 5, 2016. The amendment provides for our payment, on July 28, 2017, of $5.0 million in outstanding principal and unpaid interest due under the Loan Agreement, plus a $100,000 prepayment charge, and for our repayment, on or prior to September 30, 2017, of an additional $5.0 million outstanding principal and unpaid interest due under the Loan Agreement, plus an additional prepayment charge. We made the first $5 million payment  on July 28, 2017.  In connection with the Loan Agreement, in February 2016 we issued the lenders warrants to purchase an aggregate of up to approximately 630,000 shares of our common stock at an exercise price of $2.05 per share. Pursuant to the amendment, a portion of the warrants (representing 80% of the total number of shares issuable upon exercise of the warrants) was amended to change the exercise price of that portion of the warrants from $2.05 per share to a reduced amount, to be calculated based upon the 30-day volume-weighted average price of our common stock over the 30-day period beginning 15 days before the July 28, 2017 announcement of the NantCell license transaction.

12


Item 2. — Management's Discussion and Analysis of Financial Condition and Results of Operations
Forward Looking Statements
All statements in this Quarterly Report, including statements in this section, other than statements of historical fact are forward-looking statements, 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, 2016, 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 ("we," "us," "our," CytRx" or the "company") is a biopharmaceutical company specializing in oncology.  Our focus is on the discovery, research and clinical development of novel anti-cancer drug candidates that employ linker technologies to enhance the accumulation and release of drug at the tumor.  Aldoxorubicin, our lead clinical candidate, has been tested in over 600 patients with various types of cancer.

CytRx's lead product candidate is aldoxorubicin, a conjugate of the commonly prescribed chemotherapeutic agent doxorubicin that binds to circulating albumin in the bloodstream and is believed to concentrate the drug at the site of the tumor.  Specifically, it is comprised of (6-maleimidocaproyl) hydrazine, an acid-sensitive molecule that is conjugated to doxorubicin.  Our lead indication for aldoxorubicin is for patients with advanced soft tissue sarcomas (STS).  We met with the FDA in March 2017 to discuss a regulatory pathway for a New Drug Application (NDA) for aldoxorubicin in STS.

Aldoxorubicin has received Orphan Drug Designation (ODD) by the U.S.  FDA for the treatment of STS. ODD provides several benefits including seven years of market exclusivity after approval, certain R&D related tax credits, and protocol assistance by the FDA.  European regulators granted aldoxorubicin Orphan designation for STS which confers ten years of market exclusivity among other benefits.

On July 27, 2017, CytRx entered into an exclusive worldwide license with NantCell, Inc. ("NantCell"), granting them rights to develop, manufacture and commercialize aldoxorubicin in all indications.  As part of the license, NantCell made a strategic investment of $13 million in CytRx common stock at a premium to the market price.  CytRx is entitled to receive up to $343 million in milestones related to regulatory approvals and commercial milestones.  CytRx is entitled to receive ascending double-digit royalties for net sales for soft tissue sarcomas and mid to high single digit royalties for other indications. NantCell will take over the development and commercialization responsibility for aldoxorubicin including the NDA.
13


CytRx has an active drug discovery and research operation at our laboratory facilities in Freiburg, Germany, focusing on the creation of novel drug anti-cancer candidates by combining our proprietary linker technologies with ultra-high potency cytotoxic drugs. We are expanding our pipeline of ultra-high potency oncology candidates through our LADR™ (Linker Activated Drug Release) technology platform, a discovery engine designed to leverage CytRx's expertise in albumin biology and next generation linker technologies for the development of a new class of potential breakthrough anti-cancer therapies.

We have created a "toolbox" of linker technologies that have the ability to significantly increase the therapeutic index of ultra-high potency drugs (10-1,000 times more potent than traditional chemotherapies) by controlling the release of the drug payloads and improving drug-like properties. After infusion, these ultra-high potency drug conjugates bind to circulating albumin for transport of the drug to the tumor.  Subsequently, due to specific conditions within the tumor, the linkers are cleaved and release the anti-cancer drug payload.
 
Our current efforts are focused on two classes of ultra-high potency drug conjugates.  Our strategy across these programs is to generate additional data that will inform decisions regarding the possible selection for one or both programs for moving into human clinical trials either independently or on a partnered basis.

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, 2016. 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.
14

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.
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. On January 1, 2017, we adopted ASU 2016-09 and made a policy election to recognize forfeitures as they occur. The adoption of ASU 2016-09 did not have a material impact to the Company's financial condition or results of operations. No amounts relating to stock-based compensation have been capitalized.
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 44.8 million shares for each of the three-month and six-month periods ended June 30, 2017, and 22.4 million  shares for each of the three-month and six-month periods ended June 30, 2016, were excluded from the computation of diluted net loss per share, because the effect would be anti-dilutive.
15

Warrant Liabilities
Warrants issued in connection with the Company's July 2016 equity public offering and modified in the Company's December 2016 equity public offering are classified as liabilities as opposed to equity due to their settlement terms. These warrants are non-cash liabilities and the Company is not required to expend any cash to settle these liabilities. 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 marked to market each quarter-end until they are completely settled.The fair value of the warrants is determined using the Black-Scholes option pricing model, which requires the use of significant judgment and estimates for the inputs used in the model. The warrants issued in connection with the Company's August 2011 equity public offering expired in August 2016.
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 operation.
At June 30, 2017, we had cash and cash equivalents of approximately $55.0 million.  On July 27, 2017, we entered into a global strategic licensing agreement with NantCell Inc ("NantCell") for the exclusive rights to develop, manufacture and commercialize aldoxorbuicin for all indications. Under the terms of this Agreement, NantCell made a strategic investment into our Company by purchasing $13 million of our common stock. Concurrently, we announced the signing of an amendment to the Loan Services Agreement with Hercules whereby we made an immediate principal repayment of $5 million, a further $5 million repayment by September 30, 2017, and an updated schedule of monthly installments with a new Term Loan maturity date of August 1, 2018. Under the NantCell license, NantCell agreed to assume all future costs of developing and commercializing aldoxorubicin. Management believes that our current cash and cash equivalents, along with the net proceeds of the common stock purchase (See Note 13), 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 2017 and the first seven months of 2018 of approximately $35.6 million, which includes approximately $4.7 million for our clinical programs for aldoxorubicin, approximately $3.7 million for the research and clinical development of novel anti-cancer drug candidates at our Freiburg operations, approximately $1.1 million for general operation of our clinical programs, approximately $9.4 million for other general and administrative expenses, and approximately $16.6 million for interest and payments on the term loan. 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 our licensing partner obtains marketing approval and successfully commercializes aldoxorubicin, we anticipate it could take several years, for it to generate significant recurring revenue.  We will be dependent on future financing and possible other strategic partnerships until such time, if ever, as it can generate significant recurring revenue. We have no commitments from third parties to provide 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, seek to license to other companies our product candidates or technologies that we would prefer to develop and commercialize ourself, 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, 2017 of $25.4 million as compared to a net loss in the six-months ended June 30, 2016 of $30.9 million, or a decrease of $5.5 million.  This was due primarily to a decrease in our research and  development expenditures in the current six-month period of $7.7 million as compared to comparative 2016 period, as our pivotal clinical trial program is winding down; we also realized a decrease of $4.0 million in general and administrative expenditures, offset by an increase in interest on the term loan of $1.0 million and an increase in the loss on warrant deriviative liability of  $5.0 million.
We utilized cash of approximately $135,000 for capital expenditures in the six-month period ended June 30, 2017 as compared to approximately $661,000 in the comparable 2016 period. We do not expect any significant capital spending during the next 12 months.
16

We received a net amount of $14.0 million from the proceeds of a public offering in May, 2017.  During the fiscal quarter ended June 30, 2017, we also received net proceeds from the exercise of warrants of approximately $2.8 million, compared to $0.7 million of warrant exercise net proceeds in the comparative 2016 period.  We also made principal payments on our Term Loan of $2.4 million; no such payments were made in 2016 since we were granted a twelve month principal payment deferral under the Loan Agreement that we entered into in February 2016.
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, the ability of our partner to commercialize aldoxorubicin and  our ability to identify parties that are willing and able to enter into such arrangements related to our drug development efforts in our German lab 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.
Results of Operations
We recorded a net loss of approximately $14.4 million and $25.4 million for the three-month and six-month periods ended June 30, 2017, respectively, as compared to a net loss of approximately $18.3 million and $30.9 million for the three-month and six-month periods ended June 30, 2016, respectively. The decrease of $3.9 million in our net loss during the current three-month period resulted from a reduction of $6.7 million in the expenditures related to our aldoxorubicin program, a decrease in general and administrative expenses of $3.0 million, due to a reduction in legal fees of $1.0 million and the elimination of our pre-commercial group in the second half of 2016,  offset by an increase in the loss on warrant derivative liabilities of $5.2 million and an increase in interest expenses of $0.1 million.
We recognized no licensing revenue in the three and six-month periods ended June 30, 2017 as compared to $0.1 million in the comparative 2016 periods. All future licensing fees under our current licensing agreements are dependent upon successful development milestones being achieved by the licensor. During the remainder of 2017, we do not anticipate receiving any significant licensing fees.
Research and Development
   
Three-Month Period Ended June 30,
   
Six-Month Period Ended
June 30,
 
   
2017
   
2016
   
2017
   
2016
 
   
(In thousands)
   
(In thousands)
 
Research and development expenses
 
$
5,719
   
$
11,845
   
$
11,967
   
$
19,425
 
Employee stock option expense
   
279
     
507
     
632
     
988
 
Depreciation and amortization
   
169
     
100
     
335
     
192
 
   
$
6,167
   
$
12,452
   
$
12,934
   
$
20,605
 
                                 

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 $5.7 million and $12.0 million for the three-month and six-month periods ended June 30, 2017, respectively, and $11.8 million and $19.4 million for the three-month and six-month periods ended June 30, 2016, respectively.
Research and development expenses incurred during the three-month period ended June 30, 2017 related primarily to our aldoxorubicin clinical program.  In the three-month and six-month periods ended June 30, 2017, the development expenses of our program for aldoxorubicin were $3.7 million and $7.7 million, respectively, as compared to $10.4 million and $16.2 million for the same periods in 2016, respectively. We incurred $0.9 million and $1.6 million, respectively, for the three-month and six-month periods ended June 30, 2017, for our German lab operations, as compared to $0.5 million and $1.1 million in the 2016 comparative periods. The remainder of our research and development expenses primarily related to research and development support costs. We recorded approximately $0.3 million and $0.6 million of employee stock option expense in the three-month and six-month periods ended June 30, 2017, as compared to $0.5 million and $1.0 million for the same periods in 2016, respectively.
17

General and Administrative Expenses
   
Three-Month Period Ended
June 30,
   
Six-Month Period Ended
June 30,
 
   
2017
   
2016
   
2017
   
2016
 
   
(In thousands)
   
(In thousands)
 
General and administrative expenses
 
$
2,609
   
$
3,586
   
$
5,002
   
$
6,689
 
Non-cash general and administrative expenses
   
36
     
33
     
65
     
220
 
Employee stock option expense
   
485
     
2,499
     
1,035
     
3,156
 
Depreciation and amortization
   
7
     
11
     
14
     
22
 
   
$
3,137
   
$
6,129
   
$
6,116
   
$
10,087
 

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 $2.6 million and $5.0 million for the three and six-month periods ended June 30, 2017, respectively, and $3.6 million and $6.7 million, respectively, for the same periods in 2016.
Employee stock option expense relates to options granted to retain and compensate directors, officers and other employees.  We recorded, in total, approximately $0.5 million and $1.0 million of employee stock option expense in the three-month and six-month periods ended June 30, 2017, respectively, as compared to $2.5 million and $3.2 million, respectively, for the same periods in 2016. In the three-month period ended June 30, 2016, we amended the terms of stock options of a former executive in respect of a Retirement Agreement, resulting in a one-time expense of approximately $1.9 million. We recorded approximately $36,000 and $65,000 of non-employee stock option expense in the three-month and six-month periods, ended June 30, 2017, respectively, and $33,000 and $0.2 million for the comparative 2016 periods.
Depreciation and Amortization
Depreciation expense reflects the depreciation of our equipment and furnishings.
Interest Income and Expense
Interest income was approximately $91,000 and $151,000 for the three-month and six-month periods ended June 30, 2017, respectively, as compared to $65,000 and $127,000, respectively, for the same periods in 2016. This increase was related to the increase in cash and cash equivalents and short term investments.
Interest expense was approximately $0.9 million and $2.2 million for the three-month and six-month periods ended June 30, 2017, respectively as compared to $0.7 million and $1.2 million for the comparative 2016 periods.
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, 2017, it would not have had a material effect on our results of operations or cash flows for that period.
18

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, 2017 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 weakness 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.
19

PART II — OTHER INFORMATION
Item 1. — Legal Proceedings
The disclosure set forth in Note 12 to our financial statements is herein incorporated by reference.
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.
20


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, 2017
By:
/s/ JOHN Y. CALOZ  
    Name: John Y. Caloz  
    Title: Chief Financial Officer  
       

21

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

______________________________

22
EX-31.1 2 exh31-1.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.
  CYTRX CORPORATION  
       
August 3, 2017
By:
/s/ STEVEN A. KRIEGSMAN  
    Name: Steven A. Kriegsman  
    Title: Chief Executive Officer  
       
EX-31.2 3 exh31-2.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.
  CYTRX CORPORATION  
       
August 3, 2017
By:
/s/ JOHN Y. CALOZ  
    Name: John Y. Caloz  
    Title: Chief Financial Officer  
       
EX-32.1 4 exh32-1.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, 2016 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.
  CYTRX CORPORATION  
       
August 3, 2017
By:
/s/ STEVEN A KRIEGSMAN  
    Name: Steven A. Kriegsman  
    Title: 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 exh32-2.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, 2016 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.
  CYTRX CORPORATION  
       
August 3, 2017
By:
/s/ JOHN Y. CALOZ  
    Name: John Y. Caloz  
    Title: 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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ODD provides several benefits including seven years of market exclusivity after approval, certain R&amp;D related tax credits, and protocol assistance by the FDA.&#160;European regulators granted aldoxorubicin Orphan designation for STS which confers ten years of market exclusivity among other benefits.</div><div><br /></div><div style="font-size: 10pt; font-family: 'Times New Roman', Times, serif; text-align: left; text-indent: 36pt;">On July 27, 2017, CytRx entered into an exclusive worldwide license with NantCell, Inc. 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CytRx Corp.</font>, Case No. 2:16-cv-05666 alleging that we and certain of our officers violated the Securities Exchange Act of 1934 by allegedly making materially false and/or misleading statements, and/or failing to disclose material adverse facts to the effect that the clinical hold placed on the Phase 3 trial of aldoxorubicin for STS would prevent sufficient follow-up for patients involved in the study, thus requiring further analysis, which could cause the trial's results and/or FDA approval to be materially adversely affected or delayed.&#160; The plaintiffs allege that such wrongful acts and omissions caused significant losses and damages to a class of persons and entities that acquired our securities between November 18, 2014 and July 11, 2016, and seek an award of compensatory damages, costs and expenses, including counsel and expert fees, and such other and further relief as the Court may deem just and proper. On October 26, 2016, the Court entered an Order consolidating the actions titled <font style="font-size: 10pt; font-family: 'Times New Roman', Times, serif; font-style: italic;">In re: CytRx Corporation Securities Litigation</font>, Master File No. 16-cv-05519-SJO and appointing a Lead Plaintiff and Lead Counsel. Following the filing of a first amended complaint on January 13, 2017, on March 14, 2017 the Company and the individual defendants filed a Motion to Dismiss.&#160; Plaintiff filed an Opposition thereto on April 28, 2017.&#160;The Company and the individual defendants filed a Reply on May 30, 2017 and the matter was heard by the Court on June 12, 2017. On June 14, 2017, the Court issued an Order granting the Motion to Dismiss with leave to amend. Plaintiff filed a Second Amended Complaint and the Individual Defendants filed a renewed Motion to Dismiss. Plaintiff filed an Opposition thereto on July 24, 2017. 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In the six-month period ended June 30, 2017, the contractual term of the options granted was ten years. The dividend yield assumption of zero is based upon the fact we have never paid cash dividends and presently have no intention to do so.&#160; 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, 2016, we estimated annualized forfeiture rates of 10% for options granted to our 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&#160; Compensation costs will be adjusted for future changes in estimated forfeitures.&#160; We 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. On January 1, 2017, we adopted ASU 2016-09 and made a policy election to recognize forfeitures as they occur. The adoption of ASU 2016-09 did not have a material impact to the Company's financial condition or results of operations. No amounts relating to stock-based compensation have been capitalized.</div><div style="margin-bottom: 12pt; font-size: 10pt; font-family: 'Times New Roman', Times, serif; text-align: left; text-indent: 36pt;">As of June 30, 2017, there remained approximately $2.4 million of unrecognized compensation expense related to unvested stock options granted to current and former employees, directors, to be recognized as expense over a weighted-average period of 1.01 years. 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font-family: 'Times New Roman', Times, serif;">$</div></td><td valign="bottom" style="vertical-align: bottom; padding-bottom: 4px; text-align: right; width: 9%; background-color: #cceeff;"><div style="font-size: 10pt; font-family: 'Times New Roman', Times, serif;">2.75</div></td><td nowrap="nowrap" valign="bottom" style="vertical-align: bottom; padding-bottom: 4px; text-align: left; width: 1%; background-color: #cceeff;">&#160;</td></tr></table><div><br /></div><div style="margin-bottom: 12pt; font-size: 10pt; font-family: 'Times New Roman', Times, serif; text-align: left; text-indent: 36pt;">The aggregate intrinsic value of all outstanding options and vested options as of June 30, 2017 was $0.8 million and $0.3 million, respectively, representing options with exercise prices of less than the closing fair market value of our common stock on June 30, 2017 of $0.63 per share.</div><div style="margin-bottom: 12pt; font-size: 10pt; font-family: 'Times New Roman', Times, serif; text-align: left; text-indent: 36pt;">There were 27,989,723 and 32,502,790 warrants outstanding at June 30, 2017 and December 31, 2016, respectively both at a weighted-average exercise price of $0.68.</div><div style="margin-bottom: 12pt; font-size: 10pt; font-family: 'Times New Roman', Times, serif; font-weight: bold; text-align: left; text-indent: 14.4pt;">Restricted Stock</div><div style="margin-bottom: 12pt; font-size: 10pt; font-family: 'Times New Roman', Times, serif; text-align: left; text-indent: 36pt;">In December 2016, the Company granted to our Chairman and Chief Executive Officer, 2,325,581 shares of restricted common stock, pursuant to the 2008 Plan. 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The updated guidance requires that when substantially all of the fair value of the gross assets acquired (or disposed of) is concentrated in a single identifiable asset or a group of similar identifiable assets, the set is not a business. This updated guidance is expected to reduce the number of transactions that need to be further evaluated as business combinations. If further evaluation is necessary, the updated guidance will require that a business set include, at a minimum, an input and a substantive process that together significantly contribute to the ability to create output. The updated guidance will remove the evaluation of whether a market participant could replace missing elements. The new guidance is effective for annual and interim periods beginning after December 15, 2017 and is to be applied on a prospective basis. 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Instead, those entities would be required to disclose the amount of goodwill allocated to each reporting unit with a zero or negative carrying amount. The new guidance is effective for intrerim or annual goodwill impairment tests performed in fiscal years beginning after December 15, 2019, with early adoption permitted. We are currently evaluating the new guidance.</div><div><br /></div><div style="margin-bottom: 12pt; font-size: 10pt; font-family: 'Times New Roman', Times, serif; text-align: left; text-indent: 36pt;">In March 2016, the FASB issued Accounting Standards Update 2016-09, <font style="font-size: 10pt; font-family: 'Times New Roman', Times, serif; font-style: italic;">Compensation&#8212;Stock Compensation</font> ("ASU 2016-09"). ASU 2016-09 includes several areas of simplification to stock compensation including simplifications to the accounting for income taxes, classification of excess tax benefits on the Statement of Cash Flows and forfeitures. 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Liquidity and Capital Resources [Text Block] Liquidity and Capital Resources Schedule that describes that estimated projected expenditure by an entity. Estimated projected expenditures [Table] Estimated Projected Expenditures [Table] Represents the agent, with whom loan agreement is made. Hercules Technology Growth Capital, Inc. and Hercules Technology III, L.P. [Member] Hercules Technology Growth Capital, Inc. and Hercules Technology III, L.P. [Member] Represents the company, with whom loan agreement is made. NantCell, Inc [Member] NantCell, Inc [Member] Refers to currently projected expenditures for clinical programs for other programs. Other Programs [Member] Refers to currently projected expenditures for interest and payments on term loan. Interest and Term Loan Payment [Member] Refers to currently projected expenditures for clinical programs for other general and administrative expenses. 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Document and Entity Information - shares
6 Months Ended
Jun. 30, 2017
Aug. 03, 2017
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   165,710,526
Document Fiscal Year Focus 2017  
Document Fiscal Period Focus Q2  
Document Type 10-Q  
Amendment Flag false  
Document Period End Date Jun. 30, 2017  
XML 13 R2.htm IDEA: XBRL DOCUMENT v3.7.0.1
CONDENSED BALANCE SHEETS (Unaudited) - USD ($)
Jun. 30, 2017
Dec. 31, 2016
Current assets:    
Cash and cash equivalents $ 54,972,846 $ 56,959,485
Receivables 47,631 183,703
Prepaid expenses and other current assets 1,782,141 3,434,238
Total current assets 56,802,618 60,577,426
Equipment and furnishings, net 1,323,579 1,959,667
Goodwill 183,780 183,780
Other assets 38,014 48,911
Total assets 58,347,991 62,769,784
Current liabilities:    
Accounts payable 7,080,080 6,406,445
Accrued expenses and other current liabilities 2,972,082 3,830,498
Warrant liabilities 6,567,080 3,789,391
Term loan, net - current 6,701,040 5,481,656
Total current liabilities 23,320,282 19,507,990
Long term loan, net 15,813,507 18,484,510
Total liabilities 39,133,789 37,992,500
Commitments and contingencies
Stockholders' equity:    
Common stock, $0.001 par value, 250,000,000 shares authorized; 153,127,389 shares issued and outstanding at June 30, 2017; 111,322,895 shares issued and outstanding at December 31, 2016 153,126 111,321
Additional paid-in capital 460,329,472 437,423,958
Accumulated deficit (441,268,396) (415,865,995)
Total stockholders' equity 19,214,202 24,777,284
Total liabilities and stockholders' equity 58,347,991 62,769,784
Series A Junior Participating Preferred Stock [Member]    
Stockholders' equity:    
Preferred Stock 0 0
Series B Convertible Preferred Shares [Member]    
Stockholders' equity:    
Preferred Stock $ 0 $ 3,108,000
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CONDENSED BALANCE SHEETS (Unaudited) (Parenthetical) - USD ($)
Jun. 30, 2017
Dec. 31, 2016
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
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) 153,127,389 111,322,895
Common stock, shares outstanding (in shares) 153,127,389 111,322,895
Series A Junior Participating Preferred Stock [Member]    
Stockholders' equity:    
Preferred Stock, shares authorized (in shares) 25,000 25,000
Series B Convertible Preferred Shares [Member]    
Stockholders' equity:    
Preferred Stock, stated value $ 1,000 $ 1,000
Preferred Stock, shares authorized (in shares) 3,900 3,900
Preferred Stock, shares outstanding (in shares) 0 3,108
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CONDENSED STATEMENTS OF OPERATIONS (Unaudited) - USD ($)
3 Months Ended 6 Months Ended
Jun. 30, 2017
Jun. 30, 2016
Jun. 30, 2017
Jun. 30, 2016
Revenue:        
License revenue $ 0 $ 100,000 $ 0 $ 100,000
Expenses:        
Research and development 6,167,074 12,452,340 12,934,058 20,604,559
General and administrative 3,137,008 6,128,904 6,116,063 10,087,340
Total expenses 9,304,082 18,581,244 19,050,121 30,691,899
Loss before other income (loss) (9,304,082) (18,481,244) (19,050,121) (30,591,899)
Other income (loss):        
Interest income 90,849 65,436 151,392 127,174
Interest expense (848,395) (741,346) (2,171,110) (1,158,148)
Other income (loss), net 7,276 (798) 3,504 6,081
Gain (loss) on warrant derivative liabilities (4,303,945) 877,729 (4,336,066) 693,457
Net loss $ (14,358,297) $ (18,280,223) $ (25,402,401) $ (30,923,335)
Basic and diluted net loss per share (in dollars per share) $ (0.10) $ (0.27) $ (0.20) $ (0.46)
Basic and diluted weighted-average shares outstanding (in shares) 139,070,329 67,398,837 126,394,244 66,893,846
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CONDENSED STATEMENTS OF CASH FLOWS (Unaudited) - USD ($)
6 Months Ended
Jun. 30, 2017
Jun. 30, 2016
Cash flows from operating activities:    
Net loss $ (25,402,401) $ (30,923,335)
Adjustments to reconcile net loss to net cash used in operating activities:    
Depreciation and amortization 348,843 213,964
Stock-based compensation expense 1,731,484 4,364,886
Fair value adjustment on warrant liabilities 4,336,066 (693,457)
Non-cash litigation settlement due in common stock 0 700,000
Amortization of loan cost and discount 975,743 208,148
Loss on retirement of fixed assets 421,843 3,388
Changes in assets and liabilities:    
Receivables 136,072 4,368,773
Interest receivable 0 28,130
Prepaid expenses and other current assets 1,662,994 1,432,127
Accounts payable 673,635 (844,373)
Accrued expenses and other current liabilities (1,026,781) (4,297,864)
Net cash used in operating activities (16,142,502) (25,439,613)
Cash flows from investing activities:    
Proceeds from the sale of short-term investments 0 35,035,420
Purchases of equipment and furnishings (134,598) (660,758)
Net cash provided by (used in) investing activities (134,598) 34,374,662
Cash flows from financing activities:    
Proceeds from public offering 13,951,218 0
Proceeds from term loan, net 0 24,012,078
Payment of principal on term loan (2,427,362) 0
Net proceeds from exercise of warrants and stock options 2,766,605 704,700
Net cash provided by financing activities 14,290,461 24,716,778
Net increase (decrease) in cash and cash equivalents (1,986,639) 33,651,827
Cash and cash equivalents at beginning of period 56,959,485 22,261,372
Cash and cash equivalents at end of period 54,972,846 55,913,199
Supplemental disclosure of cash flow information:    
Cash paid during the year for interest 1,212,219 752,083
Cash paid for income taxes 800 800
Supplemental disclosure of non-cash activities:    
Warrant liability exercise 1,558,377 0
Preferred stock conversion 7,400 0
Warrants issued in connection with term loan 0 633,749
Equipment and furnishings purchased on credit 0 79,247
Shares issued in connection with the class action settlement $ 0 $ 4,500,000
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Description of Company and Basis of Presentation
6 Months Ended
Jun. 30, 2017
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 ("we," "us," "our," CytRx" or the "company") is a biopharmaceutical company specializing in oncology.  Our focus is on the discovery, research and clinical development of novel anti-cancer drug candidates that employ linker technologies to enhance the accumulation and release of drug at the tumor.  Aldoxorubicin, our lead clinical candidate, has been tested in over 600 patients with various types of cancer.

CytRx's lead product candidate is aldoxorubicin, a conjugate of the commonly prescribed chemotherapeutic agent doxorubicin that binds to circulating albumin in the bloodstream and is believed to concentrate the drug at the site of the tumor.  Specifically, it is comprised of (6-maleimidocaproyl) hydrazine, an acid-sensitive molecule that is conjugated to doxorubicin.  Our lead indication for aldoxorubicin is for patients with advanced soft tissue sarcomas (STS). We met with the FDA in March 2017 to discuss a regulatory pathway for a New Drug Application (NDA) for aldoxorubicin in STS.

Aldoxorubicin has received Orphan Drug Designation (ODD) by the U.S. FDA for the treatment of STS. ODD provides several benefits including seven years of market exclusivity after approval, certain R&D related tax credits, and protocol assistance by the FDA. European regulators granted aldoxorubicin Orphan designation for STS which confers ten years of market exclusivity among other benefits.

On July 27, 2017, CytRx entered into an exclusive worldwide license with NantCell, Inc. ("NantCell"), granting them rights to develop, manufacture and commercialize aldoxorubicin in all indications.  As part of the license, NantCell made a strategic investment of $13 million in CytRx common stock $1.10 per share, a premium of 92% to the market price on that date.  CytRx is entitled to receive up to $343 million in milestones related to regulatory approvals and commercial milestones.  CytRx is entitled to receive ascending double-digit royalties for net sales for soft tissue sarcomas and mid to high single digit royalties for other indications.  NantCell will take over the development, manufacturing and commercialization responsibility for aldoxorubicin including the cost of filing the NDA.

CytRx has an active drug discovery and research operation at our laboratory facilities in Freiburg, Germany, focusing on the creation of novel drug anti-cancer candidates by combining our proprietary linker technologies with ultra-high potency cytotoxic drugs. We are expanding our pipeline of ultra-high potency oncology candidates through our LADR™ (Linker Activated Drug Release) technology platform, a discovery engine designed to leverage CytRx's expertise in albumin biology and next generation linker technologies for the development of a new class of potential breakthrough anti-cancer therapies.

We have created a "toolbox" of linker technologies that have the ability to significantly increase the therapeutic index of ultra-high potency drugs (10-1,000 times more potent than traditional chemotherapies) by controlling the release of the drug payloads and improving drug-like properties. After infusion, these ultra-high potency drug conjugates bind to circulating albumin for transport of the drug to the tumor.  Subsequently, due to specific conditions within the tumor, the linkers are cleaved and release the anti-cancer drug payload.

Our current efforts are focused on two classes of ultra-high potency drug conjugates.  Our strategy across these programs is to generate additional pre-clinical data that will allow us to make informed decisions regarding the selection of one or both programs for moving into human clinical trials either independently or on a partnered basis.

The accompanying condensed financial statements at June 30, 2017 and for the three-month and six-month periods ended June 30, 2017 and 2016, 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, 2016 have been derived from the our audited financial statements as of that date.
The financial statements included herein have been prepared by us 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, 2016.
As a result of the worldwide license of all of our rights to aldoxorubicin to NantCell, NantCell will take over the development, manufacturing and commercialization responsibility for aldoxorubicin, thereby enabling us to eliminate our future research and development activities related to aldoxorubicin. Currently, our only research and development activities are conducted by our Freiburg, Germany, laboratory facility.  For this reason and others, our operating expenses are expected to be significantly lower in the near future. Therefore, period-to-period comparisons should not be relied upon as predictive of the results in future periods.
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Foreign Currency Remeasurement
6 Months Ended
Jun. 30, 2017
Foreign Currency Remeasurement [Abstract]  
Foreign Currency Remeasurement
2. Foreign Currency Remeasurement
The U.S. dollar has been determined to be the functional currency for the net assets of our German laboratory facilty. 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 current 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 $6,200 and $1,300, respectively, for the three-month and six-month periods ended June 30, 2017 and a gain of approximately $600 and $5,800, respectively, for the three and six-month periods ended June 30, 2016, respectively. The Company does not engage in currency hedging transactions.
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Recent Accounting Pronouncements
6 Months Ended
Jun. 30, 2017
Recent Accounting Pronouncements [Abstract]  
Recent Accounting Pronouncements
3. Recent Accounting Pronouncements
In January 2017, the FASB issued updated guidance to clarify the definition of a business within the context of business combinations. The updated guidance requires that when substantially all of the fair value of the gross assets acquired (or disposed of) is concentrated in a single identifiable asset or a group of similar identifiable assets, the set is not a business. This updated guidance is expected to reduce the number of transactions that need to be further evaluated as business combinations. If further evaluation is necessary, the updated guidance will require that a business set include, at a minimum, an input and a substantive process that together significantly contribute to the ability to create output. The updated guidance will remove the evaluation of whether a market participant could replace missing elements. The new guidance is effective for annual and interim periods beginning after December 15, 2017 and is to be applied on a prospective basis. We are currently evaluating the new guidance.

In January 2017, the FASB issued updated guidance which eliminated Step 2 from the goodwill impairment test. Step 2 is the process of measuring a goodwill impairment loss by comparing the implied fair value of a reporting unit's goodwill with the carrying amount of that goodwill. The new guidance requires entities to measure a goodwill impairment loss as the amount by which a reporting unit's carrying value exceeds its fair value, limited to the carrying amount of goodwill. The FASB also eliminated the requirements for entities that have reporting units with zero or negative carrying amounts to perform a qualitiative assessment for the goodwill impairment test. Instead, those entities would be required to disclose the amount of goodwill allocated to each reporting unit with a zero or negative carrying amount. The new guidance is effective for intrerim or annual goodwill impairment tests performed in fiscal years beginning after December 15, 2019, with early adoption permitted. We are currently evaluating the new guidance.

In March 2016, the FASB issued Accounting Standards Update 2016-09, Compensation—Stock Compensation ("ASU 2016-09"). ASU 2016-09 includes several areas of simplification to stock compensation including simplifications to the accounting for income taxes, classification of excess tax benefits on the Statement of Cash Flows and forfeitures. ASU 2016-09 is effective for annual reporting periods beginning after December 15, 2016. We adopted this Standard on January 1, 2017. The adoption of this Standard did not have material impact to the Company's financial position or its results of operations.
In February 2016, the FASB issued Accounting Standards Update 2016-02, Leases ("ASU 2016-02"). ASU 2016-02 allows the recognition of lease assets and lease liabilities by lessees for those leases classified as operating leases under previous GAAP. The classification criteria for distinguishing between finance leases and operating leases are substantially similar to the classification criteria for distinguishing between capital leases and operating leases in the previous leases guidance. The Update 2016-02 is effective for annual reporting periods beginning after December 15, 2018 and early adoption is permitted. We are still evaluating the effect of this update.
In January 2016, the FASB issued Accounting Standards Update 2016-01, Recognition and Measurement of Financial Assets and Financial Liabilities ("ASU 2016-01"). ASU 2016-01 eliminates the requirement to disclose the methods and significant assumptions used to estimate the fair value that is required to be disclosed for financial instruments measured at amortized cost on the balance sheet. The standard also clarifies the need to evaluate a valuation allowance on a deferred tax asset related to available-for-sale securities in combination with our other deferred tax assets. The update 2016-01 is effective for annual reporting periods beginning after December 15, 2017. The adoption of this standard is not expected to have a material impact on our financial statements.
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Term Loan
6 Months Ended
Jun. 30, 2017
Term Loan [Abstract]  
Term Loan
4. Term Loan
On February 5, 2016, we entered into a loan and security agreement with Hercules Technology Growth Capital, Inc. ("HTGC"), as administrative agent and lender, and Hercules Technology III, L.P., as lender ("Hercules"), pursuant to which the lenders made term loans to us on February 8, 2016 in the aggregate principal amount of $25 million (the "Term Loans"). 
The Term Loans bear interest at the daily variable rate per annum equal to 6.0% plus the prime rate, or 10.25%, whichever is greater.  We are required to make interest-only payments on the Term Loans through February 28, 2017, and beginning on March 1, 2017 blended equal monthly installments of principal amortization and accrued interest until the maturity date of the Term Loans on February 1, 2020.  Under the terms of the loan, we are required to maintain a minimum cash balance equal to the greater of (i) $10 million or (ii) forward three months projected cash burn. As security under our obligations, we issued to the lenders warrants to purchase a total of 634,146 shares of our common stock at an exercise price of $2.05. These warrants are classified as equity warrants with a fair value of $633,749.  All outstanding principal and accrued interest on the term loans will be due and payable in full on the maturity date of February 1, 2020.
As security for our obligations under the loan and securities agreement, we granted HTGC, as administrative agent, a security interest in substantially all of our existing and after-acquired assets except for our intellectual property and certain other excluded assets. The loan and security agreement contains customary representations, warranties and covenants.
  
June 30, 2017
  
December 31, 2016
 
Term Loan Principal – Current
 
$
7,737,492
  
$
6,214,057
 
Issuance Cost/Loan Discount – Current
  
(1,036,452
)
  
(732,401
)
Term Loan, Net – Current
 
$
6,701,040
  
$
5,481,656
 
         
Long Term Loan Principal
 
$
14,835,146
  
$
18,785,943
 
End Fee Payable
  
1,771,250
   
1,771,250
 
Long Term Loan Discount/Issuance Cost
  
(792,889
)
  
(2,072,683
)
Long Term Loan, Net
 
$
15,813,507
  
$
18,484,510
 

On July 28, 2017, we entererd into an Amended Loan Services Agreement with the lenders of the Term Loans whereby we agreed to make an immediate payment of $5 million of principal and unpaid interest, a further $5 million payment of principal and unpaid interest by September 30, 2017, and agreed to an updated schedule of monthly payments and a new maturity date of August 1, 2018.
The interest expense on the loan for the three-month and six-month periods ended June 30, 2017 was $848,395 and $2,171,110, respectively, as compared to $741,346 and $1,158,148 for comparative 2016 periods.
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Basic and Diluted Net Loss Per Common Share
6 Months Ended
Jun. 30, 2017
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 and warrants) 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 44.8 million shares for each of the three-month and six-month periods ended June 30, 2017, and 22.4 million shares for each of the three-month and six-month periods ended June 30, 2016.
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Warrant Liabilities
6 Months Ended
Jun. 30, 2017
Warrant Liabilities [Abstract]  
Warrant Liabilities
6. Warrant Liabilities
Liabilities measured at fair value on a recurring basis include warrant liabilities resulting from our equity financings.  In accordance with ASC 815-40, Derivatives and Hedging – Contracts in Entity's Own Equity ("ASC 815-40"), the warrant liabilities are 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. We recognized a loss of $4.3 million and a gain of $0.9 million for the three-month periods ended June 30, 2017 and 2016, respectively, and a loss of $4.3 million and a gain of $0.7 million for the six-month periods ended June 30, 2017 and 2016, respectively. The following reflects the weighted-average assumptions for each of the six-month periods indicated:
  
Six Months Ended June 30,
 
  
2017
  
2016
 
       
Risk-free interest rate
  
1.13
%
  
0.20
%
Expected dividend yield
  
0
%
  
0
%
Expected lives
  
0.79
   
0.09
 
  Expected volatility
  
125.3
%
  
59.3
%
  Warrants classified as liabilities (in shares)
  
24,110,577
   
6,371,854
 
         
Our computation of expected volatility is based on the historical daily volatility of our publicly traded stock. The dividend yield assumption of zero is based upon the fact that we have never paid cash dividends and presently have 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.
On July 19, 2017, 6,340,148 warrants expired.
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Stock Based Compensation
6 Months Ended
Jun. 30, 2017
Stock Based Compensation [Abstract]  
Stock Based Compensation
7. Stock Based Compensation
We have a 2000 Long-Term Incentive Plan, which expired on August 6, 2010.  As of June 30, 2017, there were approximately 0.4 million shares subject to outstanding stock options under this plan.  No further shares are available for future grant under this plan.
We also have a 2008 Stock Incentive Plan.  As of June 30, 2017, there were 16.4 million shares subject to outstanding stock options and 2.5 million shares outstanding related to restricted stock grants options and 10.4 million shares available for future grant under this plan.
We follow 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, we recognize 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 our Condensed Statements of Operations:
  
Three Months Ended June 30,
  
Six Months Ended June 30,
 
  
2017
  
2016
  
2017
  
2016
 
Research and development — employee
 
$
278,533
  
$
507,195
  
$
631,616
  
$
988,006
 
General and administrative — employee
  
401,820
   
2,499,368
   
869,485
   
3,156,418
 
Total employee stock-based compensation
 
$
680,353
  
$
3,006,563
  
$
1,501,101
  
$
4,144,424
 
                 
Research and development — non-employee
 
$
  
$
  
$
  
$
 
General and administrative — non-employee
  
36,578
   
32,506
   
65,237
   
220,462
 
Total non-employee stock-based compensation
 
$
36,578
  
$
32,506
  
$
65,237
  
$
220,462
 

During the six-month period ended June 30, 2017, we granted stock options to purchase 10,000 shares of our common stock at an average weighted exercise price of $0.41. During the six-month period ended June 30, 2016, we granted stock options to purchase 425,000 shares of our common stock and warrants to purchase 500,000 shares of our common stock at a weighted average exercise price of $1.74. In the three-month period ended June 30, 2016, we amended the terms of stock options of a former executive in respect of a Retirement Agreement, resulting in a one-time expense of approximately $1.9 million.
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, 2017
  
Six Months Ended June 30, 2016
 
Risk-free interest rate
  
2.04
%
  
1.47
%
Expected volatility
  
85.5
%
  
76.3
%
Expected lives (years)
  
6
   
5 - 10
 
Expected dividend yield
  
0.00
%
  
0.00
%
         
 
Our computation of expected volatility is based on the historical daily volatility of our publicly traded stock.  We use historical information to compute expected lives. In the six-month period ended June 30, 2017, the contractual term of the options granted was ten years. The dividend yield assumption of zero is based upon the fact we have never paid cash dividends and presently have 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, 2016, we estimated annualized forfeiture rates of 10% for options granted to our 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  Compensation costs will be adjusted for future changes in estimated forfeitures.  We 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. On January 1, 2017, we adopted ASU 2016-09 and made a policy election to recognize forfeitures as they occur. The adoption of ASU 2016-09 did not have a material impact to the Company's financial condition or results of operations. No amounts relating to stock-based compensation have been capitalized.
As of June 30, 2017, there remained approximately $2.4 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 1.01 years. Presented below is our stock option activity:
  
Six Months Ended June 30, 2017
 
  
Number of Options (Employees)
  
Number of Options (Non-Employees)
  
Total Number of Options
  
Weighted-Average Exercise Price
 
Outstanding at January 1, 2017
  
16,879,770
   
600,000
   
17,479,770
  
$
2.37
 
Granted
  
10,000
   
   
10,000
  
$
0.41
 
Exercised, Forfeited or Expired
  
(646,847
)
  
   
(646,847
)
 
$
3.16
 
Outstanding at June 30, 2017
  
16,242,923
   
600,000
   
16,842,932
  
$
2.34
 
Options exercisable at June 30, 2017
  
11,655,168
   
600,000
   
12,255,168
  
$
2.75
 


The following table summarizes significant ranges of outstanding stock options under our plans at June 30, 2017:

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
 
$
0.41 - $1.50
   
4,317,533
   
9.45
  
$
0.44
   
1,586,461
   
9.46
  
$
0.44
 
$
1.51 – $2.50
   
8,669,296
   
7.32
  
$
2.26
   
6,835,946
   
7.07
  
$
2.22
 
$
2.51 – $4.00
   
960,670
   
6.64
  
$
2.88
   
937,337
   
6.61
  
$
2.87
 
$
4.01 – $32.55
   
2,895,424
   
5.69
  
$
5.24
   
2,895,424
   
5.69
  
$
5.24
 
     
16,842,923
   
7.55
  
$
2.34
   
12,255,168
   
7.02
  
$
2.75
 

The aggregate intrinsic value of all outstanding options and vested options as of June 30, 2017 was $0.8 million and $0.3 million, respectively, representing options with exercise prices of less than the closing fair market value of our common stock on June 30, 2017 of $0.63 per share.
There were 27,989,723 and 32,502,790 warrants outstanding at June 30, 2017 and December 31, 2016, respectively both at a weighted-average exercise price of $0.68.
Restricted Stock
In December 2016, the Company granted to our Chairman and Chief Executive Officer, 2,325,581 shares of restricted common stock, pursuant to the 2008 Plan. This restricted stock vests in equal annual instalments over three years.  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 stock on the grant date was $1,000,000. The Company recorded an employee stock-based compensation expense for restricted stock of approximately $83,029 and $165,146 respectively, for the three and six-month periods ended June 30, 2017 as compared to zero for the comparative 2016 periods.
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Fair Value Measurements
6 Months Ended
Jun. 30, 2017
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, 2017 for assets and liabilities measured at fair value on a recurring basis:
(In thousands)
 
Level I
  
Level II
  
Level III
  
Total
 
Cash equivalents
 
$
53,485
  
$
  
$
  
$
53,485
 
Warrant liabilities
  
   
   
(6,567
)
  
(6,567
)

The following table summarizes fair value measurements by level at December 31, 2016 for assets and liabilities measured at fair value on a recurring basis:
(In thousands)
 
Level I
  
Level II
  
Level III
  
Total
 
Cash equivalents
 
$
56,276
  
$
  
$
  
$
56,276
 
Warrant liabilities
  
   
   
(3,789
)
  
(3,789
)

Liabilities measured at market value on a recurring basis include warrant liabilities resulting from recent debt and equity financings. In accordance with ASC 815-40, the warrant liabilities 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 our application of ASC 505-50. The $2.8 million increase in fair value of the warrant liabilities is due to the significant excess of the exercise price over the Company's stock price as of June 30, 2017 and the close proximity to the expiration date of the warrants (see Note 6).
We consider carrying amounts of accounts receivable, accounts payable and accrued expenses to approximate fair value due to the short-term nature of these financial instruments.  
Our 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.  Our non-financial assets were not material at June 30, 2017 or 2016.
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Liquidity and Capital Resources
6 Months Ended
Jun. 30, 2017
Liquidity and Capital Resources [Abstract]  
Liquidity and Capital Resources
9. Liquidity and Capital Resources
At June 30, 2017, we had cash and cash equivalents of approximately $55.0 million.  On July 27, 2017, we entered into a global strategic licensing agreement with NantCell Inc ("NantCell") for the exclusive rights to develop, manufacture and commercialize aldoxorbuicin for all indications. Under the terms of this Agreement, NantCell made a strategic investment into our Company by purchasing $13 million of our common stock. Concurrently, we announced the signing of an amendment to the Loan Services Agreement with Hercules whereby we made an immediate principal repayment of $5 million, a further $5 million repayment by September 30, 2017, and an updated schedule of monthly instalments with a new Term Loan maturity date of August 1, 2018. Under the NantCell license, NantCell agreed to assume all future costs of developing and commercializing aldoxorubicin. Management believes that our current cash and cash equivalents, along with the net proceeds of the common stock purchase (See Note 13), 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 2017 and the first seven months of 2018 of approximately $35.6 million, which includes approximately $4.7 million for our clinical programs for aldoxorubicin, approximately $3.7 million for the research and clinical development of novel anti-cancer drug candidates at our Freiburg operations, approximately $1.1 million for general operation of our clinical programs, approximately $9.4 million for other general and administrative expenses, and approximately $16.6 million for interest and payments on the term loan. 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 our licensing partner obtains marketing approval and successfully commercializes aldoxorubicin, we anticipate it could take several years, for it to generate significant recurring revenue.  We will be dependent on future financing and possible other strategic partnerships until such time, if ever, as it can generate significant recurring revenue. We have no commitments from third parties to provide 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, seek to license to other companies our product candidates or technologies that we would prefer to develop and commercialize ourself, or seek to sell some or all of our assets or merge with or be acquired by another company.
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Equity Transactions
6 Months Ended
Jun. 30, 2017
Equity Transactions [Abstract]  
Equity Transactions
10. Equity Transactions
In the first quarter of 2017, there were 3,108 shares of our outstanding Series B Convertible Preferred converted by the holders into 7.4 million shares of our common stock.
In the second quarter of 2017, there were 4,404,494 shares of our common stock issued from the exercise of warrants.
On May 2, 2017, we issued 30.0 million shares of our common stock in a public offering.
As of June 30, 2017, we have reserved approximately 10.4 million of our authorized but unissued shares of common stock for future issuance pursuant to our employee stock option plans issued to employees and consultants.
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Income Taxes
6 Months Ended
Jun. 30, 2017
Income Taxes [Abstract]  
Income Taxes
11. Income Taxes
At December 31, 2016, we had federal and state net operating loss carryforwards as of  $339.0 million and $224.0 million, respectively, available to offset against future taxable income, which expire in 2017 through 2036, of which $152.0 million and $145.0 million, respectively, are not subject to limitation under Section 382 of the Internal Revenue Code.
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Commitments and contingencies
6 Months Ended
Jun. 30, 2017
Commitments and contingencies [Abstract]  
Commitments and contingencies
12. Commitments and contingencies
Commitments
We have an agreement with KTB Tumorforschungs GmbH, or KTB, for the Company's exclusive license of patent rights held by KTB for the worldwide development and commercialization of aldoxorubicin. Under the agreement, we must make payments to KTB in the aggregate of $6.0 million upon meeting clinical and regulatory milestones up to and including the product's second final marketing approval.  We also have 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 we obtain.
In the event that we must pay a third party in order to exercise our right to the intellectual property under the agreement, we will deduct a percentage of those payments from the royalties due KTB, up to an agreed upon cap. As a result of the NantCell license and the sale of $13 million of our shares to NantCell, we will incur an obligation to pay KTB approximately $0.6 million.
Contingencies
We applied the disclosure provisions of ASC 460, Guarantees ("ASC 460") to our agreements that contain guarantees or indemnities by us. We provide (i) indemnifications of varying scope and size to certain investors and other parties for certain losses suffered or incurred by the indemnified party in connection with various types of third-party claims; and (ii) indemnifications of varying scope and size to officers and directors against third party claims arising from the services they provide to us.
 
Shareholder Derivative Actions in Delaware.  There are two competing derivative complaints pending in the Delaware Court of Chancery alleging claims related to our alleged retention of DreamTeamGroup and MissionIR.  On December 14, 2015, a shareholder derivative complaint, captioned Niedermeyer et al. v. Kriegsman et al., C.A. No. 11800, was filed against certain of our officers and directors, for which a second amended complaint was filed on October 12, 2016.  On September 6, 2016, one of the plaintiffs in the California litigation (discussed above) effectively refiled his complaint in the Delaware Court of Chancery, with the case captioned Taylor v. Kriegsman, C.A. No. 12720.  Following competing motions for appointment of a lead plaintiff and lead counsel, On February 22, 2017, the Court of Chancery appointed Niedermeyer et al.as lead plaintiffs in the complaint. On May 3, 2017, the parties entered into negotiations with a mediator and on June 2, 2017, the parties entered into a Memorandum of Understanding ("MOU") to settle the entire action. On June 15, 2017, the MOU was submitted to the Court.
 
Class Action in California.  On July 25 and 29, 2016, nearly identical class action complaints were filed in the U.S. District Court for the Central District of California, titled Crihfield v. CytRx Corp., et al., Case No. 2:16-cv-05519 and Dorce v. CytRx Corp., Case No. 2:16-cv-05666 alleging that we and certain of our officers violated the Securities Exchange Act of 1934 by allegedly making materially false and/or misleading statements, and/or failing to disclose material adverse facts to the effect that the clinical hold placed on the Phase 3 trial of aldoxorubicin for STS would prevent sufficient follow-up for patients involved in the study, thus requiring further analysis, which could cause the trial's results and/or FDA approval to be materially adversely affected or delayed.  The plaintiffs allege that such wrongful acts and omissions caused significant losses and damages to a class of persons and entities that acquired our securities between November 18, 2014 and July 11, 2016, and seek an award of compensatory damages, costs and expenses, including counsel and expert fees, and such other and further relief as the Court may deem just and proper. On October 26, 2016, the Court entered an Order consolidating the actions titled In re: CytRx Corporation Securities Litigation, Master File No. 16-cv-05519-SJO and appointing a Lead Plaintiff and Lead Counsel. Following the filing of a first amended complaint on January 13, 2017, on March 14, 2017 the Company and the individual defendants filed a Motion to Dismiss.  Plaintiff filed an Opposition thereto on April 28, 2017. The Company and the individual defendants filed a Reply on May 30, 2017 and the matter was heard by the Court on June 12, 2017. On June 14, 2017, the Court issued an Order granting the Motion to Dismiss with leave to amend. Plaintiff filed a Second Amended Complaint and the Individual Defendants filed a renewed Motion to Dismiss. Plaintiff filed an Opposition thereto on July 24, 2017. The Company and the Individual Defendants filed a Reply on July 31, 2017 and the matter is set to be heard by the Court on August 14, 2017.
The Company intends to vigorously defend against the foregoing complaints. CytRx has directors' and officers' liability insurance, which will be utilized in the defense of these matters. 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 management's view of these matters may change in the future.
The Company evaluates developments in legal proceedings and other matters on a quarterly basis. The Company records accruals for loss contingencies to the extent that the Company concludes that it is probable that a liability has been incurred and the amount of the related loss can be reasonably estimated. The Company has accrued $0.7 million of litigation settlement related to Shareholder Derivative actions.

We evaluate developments in legal proceedings and other matters on a quarterly basis. If an unfavorable outcome becomes probable and reasonably estimable, we could incur charges that could have a material adverse impact on our financial condition and results of operations for the period in which the outcome becomes probable and reasonably estimable.
XML 29 R18.htm IDEA: XBRL DOCUMENT v3.7.0.1
Subsequent Events
6 Months Ended
Jun. 30, 2017
Subsequent Events [Abstract]  
Subsequent Events
13. Subsequent Events
On July 27, 2017, we entered into a global strategic license agreement (the "License Agreement") with NantCell, Inc. ("NantCell"), for providing NantCell the exclusive rights to develop and commercialize aldoxorubicin for all indications. Under the terms of the License Agreement, CytRx is entitled to receive up to $343 million in milestone payments related to regulatory approvals and commercial milestones for aldoxorubicin. In addition, CytRx will receive certain specified royalties for all other indications (our receipt of which would obligate us to make certain payments to KTB). NantCell will be responsible for all future development, manufacturing and commercialization expenses, other than royalties and milestones that may be owed by CytRx under its existing license agreements.
In connection with the License Agreement, on July 27, 2017, CytRx (i) entered into a stock purchase agreement with NantCell in which NantCell purchased $13 million of CytRx common stock at $1.10 per share, a 92% premium to market on that date, and (ii) issued to NantCell a warrant to purchase up to 3 million shares of common stock at $1.10, expiring on January 27, 2019.
On July 27, 2017, we entered into a First Amendment to Loan and Security Agreement with Hercules  to amend our existing long-term loan facility (the "Loan Agreement") originally entered into on February 5, 2016. The amendment provides for our payment, on July 28, 2017, of $5.0 million in outstanding principal and unpaid interest due under the Loan Agreement, plus a $100,000 prepayment charge, and for our repayment, on or prior to September 30, 2017, of an additional $5.0 million outstanding principal and unpaid interest due under the Loan Agreement, plus an additional prepayment charge. We made the first $5 million payment  on July 28, 2017.  In connection with the Loan Agreement, in February 2016 we issued the lenders warrants to purchase an aggregate of up to approximately 630,000 shares of our common stock at an exercise price of $2.05 per share. Pursuant to the amendment, a portion of the warrants (representing 80% of the total number of shares issuable upon exercise of the warrants) was amended to change the exercise price of that portion of the warrants from $2.05 per share to a reduced amount, to be calculated based upon the 30-day volume-weighted average price of our common stock over the 30-day period beginning 15 days before the July 28, 2017 announcement of the NantCell license transaction.
XML 30 R19.htm IDEA: XBRL DOCUMENT v3.7.0.1
Term Loan (Tables)
6 Months Ended
Jun. 30, 2017
Term Loan [Abstract]  
Schedule of Term Loan
The loan and security agreement contains customary representations, warranties and covenants.
  
June 30, 2017
  
December 31, 2016
 
Term Loan Principal – Current
 
$
7,737,492
  
$
6,214,057
 
Issuance Cost/Loan Discount – Current
  
(1,036,452
)
  
(732,401
)
Term Loan, Net – Current
 
$
6,701,040
  
$
5,481,656
 
         
Long Term Loan Principal
 
$
14,835,146
  
$
18,785,943
 
End Fee Payable
  
1,771,250
   
1,771,250
 
Long Term Loan Discount/Issuance Cost
  
(792,889
)
  
(2,072,683
)
Long Term Loan, Net
 
$
15,813,507
  
$
18,484,510
 
XML 31 R20.htm IDEA: XBRL DOCUMENT v3.7.0.1
Warrant Liabilities (Tables)
6 Months Ended
Jun. 30, 2017
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,
 
  
2017
  
2016
 
       
Risk-free interest rate
  
1.13
%
  
0.20
%
Expected dividend yield
  
0
%
  
0
%
Expected lives
  
0.79
   
0.09
 
  Expected volatility
  
125.3
%
  
59.3
%
  Warrants classified as liabilities (in shares)
  
24,110,577
   
6,371,854
 
         
XML 32 R21.htm IDEA: XBRL DOCUMENT v3.7.0.1
Stock Based Compensation (Tables)
6 Months Ended
Jun. 30, 2017
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 our Condensed Statements of Operations:
  
Three Months Ended June 30,
  
Six Months Ended June 30,
 
  
2017
  
2016
  
2017
  
2016
 
Research and development — employee
 
$
278,533
  
$
507,195
  
$
631,616
  
$
988,006
 
General and administrative — employee
  
401,820
   
2,499,368
   
869,485
   
3,156,418
 
Total employee stock-based compensation
 
$
680,353
  
$
3,006,563
  
$
1,501,101
  
$
4,144,424
 
                 
Research and development — non-employee
 
$
  
$
  
$
  
$
 
General and administrative — non-employee
  
36,578
   
32,506
   
65,237
   
220,462
 
Total non-employee stock-based compensation
 
$
36,578
  
$
32,506
  
$
65,237
  
$
220,462
 
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, 2017
  
Six Months Ended June 30, 2016
 
Risk-free interest rate
  
2.04
%
  
1.47
%
Expected volatility
  
85.5
%
  
76.3
%
Expected lives (years)
  
6
   
5 - 10
 
Expected dividend yield
  
0.00
%
  
0.00
%
         
Schedule of Share-based Compensation, Stock Options, Activity
Presented below is our stock option activity:
  
Six Months Ended June 30, 2017
 
  
Number of Options (Employees)
  
Number of Options (Non-Employees)
  
Total Number of Options
  
Weighted-Average Exercise Price
 
Outstanding at January 1, 2017
  
16,879,770
   
600,000
   
17,479,770
  
$
2.37
 
Granted
  
10,000
   
   
10,000
  
$
0.41
 
Exercised, Forfeited or Expired
  
(646,847
)
  
   
(646,847
)
 
$
3.16
 
Outstanding at June 30, 2017
  
16,242,923
   
600,000
   
16,842,932
  
$
2.34
 
Options exercisable at June 30, 2017
  
11,655,168
   
600,000
   
12,255,168
  
$
2.75
 
Schedule of Share-based Compensation, Summarizes Significant Ranges of Outstanding Stock Options
The following table summarizes significant ranges of outstanding stock options under our plans at June 30, 2017:

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
 
$
0.41 - $1.50
   
4,317,533
   
9.45
  
$
0.44
   
1,586,461
   
9.46
  
$
0.44
 
$
1.51 – $2.50
   
8,669,296
   
7.32
  
$
2.26
   
6,835,946
   
7.07
  
$
2.22
 
$
2.51 – $4.00
   
960,670
   
6.64
  
$
2.88
   
937,337
   
6.61
  
$
2.87
 
$
4.01 – $32.55
   
2,895,424
   
5.69
  
$
5.24
   
2,895,424
   
5.69
  
$
5.24
 
     
16,842,923
   
7.55
  
$
2.34
   
12,255,168
   
7.02
  
$
2.75
 
XML 33 R22.htm IDEA: XBRL DOCUMENT v3.7.0.1
Fair Value Measurements (Tables)
6 Months Ended
Jun. 30, 2017
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, 2017 for assets and liabilities measured at fair value on a recurring basis:
(In thousands)
 
Level I
  
Level II
  
Level III
  
Total
 
Cash equivalents
 
$
53,485
  
$
  
$
  
$
53,485
 
Warrant liabilities
  
   
   
(6,567
)
  
(6,567
)

The following table summarizes fair value measurements by level at December 31, 2016 for assets and liabilities measured at fair value on a recurring basis:
(In thousands)
 
Level I
  
Level II
  
Level III
  
Total
 
Cash equivalents
 
$
56,276
  
$
  
$
  
$
56,276
 
Warrant liabilities
  
   
   
(3,789
)
  
(3,789
)
XML 34 R23.htm IDEA: XBRL DOCUMENT v3.7.0.1
Description of Company and Basis of Presentation (Details)
$ / shares in Units, $ in Millions
6 Months Ended
Jul. 27, 2017
USD ($)
$ / shares
Jun. 30, 2017
USD ($)
Patient
Class
Description of Company and Basis of Presentation [Abstract]    
Number of patients tested for various types of cancer | Patient   600
Number of years Orphan Drug Designation provides several benefits of market exclusivity after approval   7 years
Number of years soft tissue sarcomas confers market among other benefits   10 years
Subsequent Event [Line Items]    
Number of classes of ultra-high potency drug conjugates | Class   2
NantCell, Inc [Member]    
Subsequent Event [Line Items]    
Net proceeds received from the sale of common stock   $ 13.0
Subsequent Event [Member] | NantCell, Inc [Member]    
Subsequent Event [Line Items]    
Net proceeds received from the sale of common stock $ 13.0  
Common stock, share price (in dollars per share) | $ / shares $ 1.10  
Percentage of common stock premium at market price 92.00%  
Subsequent Event [Member] | NantCell, Inc [Member] | Maximum [Member]    
Subsequent Event [Line Items]    
Milestone payments entitled to receive under license agreement $ 343.0  
XML 35 R24.htm IDEA: XBRL DOCUMENT v3.7.0.1
Foreign Currency Remeasurement (Details) - USD ($)
3 Months Ended 6 Months Ended
Jun. 30, 2017
Jun. 30, 2016
Jun. 30, 2017
Jun. 30, 2016
Foreign Currency Remeasurement [Abstract]        
Gain on foreign currency translation adjustment $ 6,200 $ 600 $ 1,300 $ 5,800
XML 36 R25.htm IDEA: XBRL DOCUMENT v3.7.0.1
Term Loan (Details) - USD ($)
2 Months Ended 3 Months Ended 6 Months Ended
Jul. 28, 2017
Jul. 27, 2017
Feb. 08, 2016
Feb. 05, 2016
Sep. 30, 2017
Jun. 30, 2017
Jun. 30, 2016
Jun. 30, 2017
Jun. 30, 2016
Dec. 31, 2016
Debt Instrument [Line Items]                    
Amount received under initial loan agreement               $ 0 $ 24,012,078  
Term Loan, Net - Current           $ 6,701,040   6,701,040   $ 5,481,656
Long Term Loan, Net           15,813,507   15,813,507   18,484,510
Debt instrument, repayment of principal and unpaid interest               2,427,362 0  
Interest expense           848,395 $ 741,346 $ 2,171,110 $ 1,158,148  
Warrants [Member]                    
Debt Instrument [Line Items]                    
Number of warrants issued (in shares)             500,000   500,000  
Warrants exercise price (in dollars per share)             $ 1.74   $ 1.74  
Hercules Technology Growth Capital, Inc. and Hercules Technology III, L.P. [Member]                    
Debt Instrument [Line Items]                    
Amount received under initial loan agreement     $ 25,000,000              
Debt instrument, interest rate       10.25%            
Debt instrument, minimum cash balance required to be maintained       $ 10,000,000            
Number of warrants issued (in shares)       630,000            
Warrants exercise price (in dollars per share)       $ 2.05            
Debt instrument, maturity date               Feb. 01, 2020    
Term Loan Principal - Current           7,737,492   $ 7,737,492   6,214,057
Issuance Cost/Loan Discount - Current           (1,036,452)   (1,036,452)   (732,401)
Term Loan, Net - Current           6,701,040   6,701,040   5,481,656
Long Term Loan Principal           14,835,146   14,835,146   18,785,943
End Fee Payable           1,771,250   1,771,250   1,771,250
Long Term Loan Discount/Issuance Cost           (792,889)   (792,889)   (2,072,683)
Long Term Loan, Net           15,813,507   15,813,507   $ 18,484,510
Interest expense           848,395 $ 741,346 2,171,110 $ 1,158,148  
Hercules Technology Growth Capital, Inc. and Hercules Technology III, L.P. [Member] | Subsequent Event [Member]                    
Debt Instrument [Line Items]                    
Debt instrument, repayment of principal and unpaid interest $ 5,000,000 $ 5,000,000                
Maturity date of amended loan servicing agreement Aug. 01, 2018                  
Hercules Technology Growth Capital, Inc. and Hercules Technology III, L.P. [Member] | Scenario, Forecast [Member]                    
Debt Instrument [Line Items]                    
Debt instrument, repayment of principal and unpaid interest         $ 5,000,000          
Hercules Technology Growth Capital, Inc. and Hercules Technology III, L.P. [Member] | Warrants [Member]                    
Debt Instrument [Line Items]                    
Number of warrants issued (in shares)       634,146            
Warrants exercise price (in dollars per share)       $ 2.05            
Fair value of warrants classified as equity warrants           $ 633,749   $ 633,749    
Hercules Technology Growth Capital, Inc. and Hercules Technology III, L.P. [Member] | Prime Rate [Member]                    
Debt Instrument [Line Items]                    
Debt instrument, basis spread on variable rate       6.00%            
XML 37 R26.htm IDEA: XBRL DOCUMENT v3.7.0.1
Basic and Diluted Net Loss Per Common Share (Details) - shares
shares in Millions
3 Months Ended 6 Months Ended
Jun. 30, 2017
Jun. 30, 2016
Jun. 30, 2017
Jun. 30, 2016
Basic and Diluted Net Loss Per Common Share [Abstract]        
Antidilutive securities excluded from computation of earnings per share (in shares) 44.8 22.4 44.8 22.4
XML 38 R27.htm IDEA: XBRL DOCUMENT v3.7.0.1
Warrant Liabilities (Details) - USD ($)
3 Months Ended 6 Months Ended
Jul. 19, 2017
Jun. 30, 2017
Jun. 30, 2016
Jun. 30, 2017
Jun. 30, 2016
Derivative [Line Items]          
Gain (loss) on warrant derivative liabilities   $ (4,303,945) $ 877,729 $ (4,336,066) $ 693,457
Subsequent Event [Member]          
Derivative [Line Items]          
Warrants expired (in shares) 6,340,148        
Warrants [Member]          
Derivative [Line Items]          
Gain (loss) on warrant derivative liabilities   $ (4,303,945) $ 877,729 $ (4,336,066) $ 693,457
Risk-free interest rate       1.13% 0.20%
Expected dividend yield       0.00% 0.00%
Expected lives       9 months 14 days 1 month 2 days
Expected volatility       125.30% 59.30%
Warrants classified as liabilities (in shares)   24,110,577 6,371,854 24,110,577 6,371,854
XML 39 R28.htm IDEA: XBRL DOCUMENT v3.7.0.1
Stock Based Compensation (Details) - USD ($)
3 Months Ended 6 Months Ended 12 Months Ended
Jun. 30, 2017
Jun. 30, 2016
Jun. 30, 2017
Jun. 30, 2016
Dec. 31, 2016
Jun. 30, 2017
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           $ 2,400,000
Unrecognized compensation cost, recognized as expense over a weighted-average period     1 year 4 days      
Stock Options [Member]            
Share-based Compensation Arrangement by Share-based Payment Award [Line Items]            
Share-based compensation, shares subject to stock options (in shares) 16,842,932   17,479,770   17,479,770 16,842,932
Share-based compensation arrangement by share-based payment award, fair value assumptions and methodology [Abstract]            
Risk-free interest rate     2.04% 1.47%    
Expected volatility     85.50% 76.30%    
Expected lives     6 years      
Expected dividend yield     0.00% 0.00%    
Contractual term     10 years      
Number of Options (Employees and Non-Employees) [Abstract]            
Outstanding at beginning of period (in shares)     17,479,770      
Granted (in shares)     10,000 425,000    
Exercised, forfeited or expired (in shares)     (646,847)      
Outstanding at end of period (in shares) 16,842,932   16,842,932   17,479,770  
Options exercisable at end of period (in shares) 12,255,168   12,255,168      
Weighted-Average Exercise Price Options [Abstract]            
Outstanding at beginning of period (in dollars per share)     $ 2.37      
Granted (in dollars per share)     0.41      
Exercised, forfeited or expired (in dollars per share)     3.16      
Outstanding at end of period (in dollars per share) $ 2.34   2.34   $ 2.37  
Options exercisable at end of period (in dollars per share) $ 2.75   $ 2.75      
Stock Options [Member] | Minimum [Member]            
Share-based compensation arrangement by share-based payment award, fair value assumptions and methodology [Abstract]            
Expected lives       5 years    
Stock Options [Member] | Maximum [Member]            
Share-based compensation arrangement by share-based payment award, fair value assumptions and methodology [Abstract]            
Expected lives       10 years    
Stock Options [Member] | Employees [Member]            
Share-based Compensation Arrangement by Share-based Payment Award [Line Items]            
Share-based compensation, shares subject to stock options (in shares) 16,242,923   16,879,770   16,879,770 16,242,923
Share-based compensation arrangement by share-based payment award, fair value assumptions and methodology [Abstract]            
Estimated annualized forfeiture rate       10.00%    
Number of Options (Employees and Non-Employees) [Abstract]            
Outstanding at beginning of period (in shares)     16,879,770      
Granted (in shares)     10,000      
Exercised, forfeited or expired (in shares)     (646,847)      
Outstanding at end of period (in shares) 16,242,923   16,242,923   16,879,770  
Options exercisable at end of period (in shares) 11,655,168   11,655,168      
Stock Options [Member] | Non-Employees [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   600,000 600,000
Share-based compensation arrangement by share-based payment award, fair value assumptions and methodology [Abstract]            
Estimated annualized forfeiture rate       0.00%    
Number of Options (Employees and Non-Employees) [Abstract]            
Outstanding at beginning of period (in shares)     600,000      
Granted (in shares)     0      
Exercised, forfeited or expired (in shares)     0      
Outstanding at end of period (in shares) 600,000   600,000   600,000  
Options exercisable at end of period (in shares) 600,000   600,000      
Stock Options [Member] | Senior Management [Member]            
Share-based compensation arrangement by share-based payment award, fair value assumptions and methodology [Abstract]            
Estimated annualized forfeiture rate       2.00%    
Stock Options [Member] | Directors [Member]            
Share-based compensation arrangement by share-based payment award, fair value assumptions and methodology [Abstract]            
Estimated annualized forfeiture rate       0.00%    
Stock Options [Member] | Former Executive [Member]            
Share-based Compensation Arrangement by Share-based Payment Award [Line Items]            
Share based compensation expense   $ 1,900,000        
Restricted Stock [Member]            
Restricted Stock [Abstract]            
Restricted stock expense $ 83,029 $ 0 $ 165,146 $ 0    
Warrants [Member]            
Share-based Compensation Arrangement by Share-based Payment Award [Line Items]            
Number of warrants issued (in shares)   500,000   500,000    
Exercise price of warrants (in dollars per share)   $ 1.74   $ 1.74    
2000 Long Term Incentive Plan [Member]            
Share-based Compensation Arrangement by Share-based Payment Award [Line Items]            
Expiration date     Aug. 06, 2010      
Share-based compensation, shares subject to stock options (in shares) 400,000   400,000     400,000
Share-based compensation, shares available for future grant (in shares)           0
Number of Options (Employees and Non-Employees) [Abstract]            
Outstanding at end of period (in shares) 400,000   400,000      
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) 16,400,000   16,400,000     16,400,000
Share-based compensation, shares available for future grant (in shares)           10,400,000
Number of Options (Employees and Non-Employees) [Abstract]            
Outstanding at end of period (in shares) 16,400,000   16,400,000      
2008 Stock Incentive Plan [Member] | Restricted Stock [Member]            
Share-based Compensation Arrangement by Share-based Payment Award [Line Items]            
Share-based compensation, outstanding stock options (in shares)           2,500,000
2008 Stock Incentive Plan [Member] | Restricted Stock [Member] | Chairman and Chief Executive Officer [Member]            
Restricted Stock [Abstract]            
Share based compensation arranged by share based payment award restricted stock granted (in shares)         2,325,581  
Vesting period         3 years  
Share based compensation of fair value of the restricted stock on the grant         $ 1,000,000  
XML 40 R29.htm IDEA: XBRL DOCUMENT v3.7.0.1
Stock Based Compensation, Schedule of Employee and Non Employee Service Share Based Compensation (Details) - Stock Options and Warrants [Member] - USD ($)
3 Months Ended 6 Months Ended
Jun. 30, 2017
Jun. 30, 2016
Jun. 30, 2017
Jun. 30, 2016
Employees [Member]        
Total stock-based compensation expense resulting from stock options and warrants [Abstract]        
Allocated employee and non-employee stock-based compensation expense, Total $ 680,353 $ 3,006,563 $ 1,501,101 $ 4,144,424
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 36,578 32,506 65,237 220,462
Research and Development Expense [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 278,533 507,195 631,616 988,006
Research and Development Expense [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] | Employees [Member]        
Total stock-based compensation expense resulting from stock options and warrants [Abstract]        
Allocated employee and non-employee stock-based compensation expense, Total 401,820 2,499,368 869,485 3,156,418
General and Administrative Expense [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 $ 36,578 $ 32,506 $ 65,237 $ 220,462
XML 41 R30.htm IDEA: XBRL DOCUMENT v3.7.0.1
Stock Based Compensation, by Exercise Price Range (Details)
$ / shares in Units, $ in Millions
6 Months Ended
Jun. 30, 2017
USD ($)
$ / shares
shares
Dec. 31, 2016
$ / shares
shares
Stock Options [Member]    
Share based compensation, shares authorized under significant ranges of outstanding stock option plans in period [Abstract]    
Number of Options (in shares) | shares 16,842,923  
Weighted-Average Remaining Contractual Life 7 years 6 months 18 days  
Weighted-Average Exercise Price (in dollars per share) $ 2.34  
Number of Options Exercisable (in shares) | shares 12,255,168  
Weighted-Average Remaining Contractual Life 7 years 7 days  
Weighted-Average Exercise Price, Options Exercisable (in dollars per share) $ 2.75  
Aggregate intrinsic value of outstanding options | $ $ 0.8  
Aggregate intrinsic value of options vested | $ $ 0.3  
Closing price of the common stock (in dollars per share) $ 0.63  
Warrants [Member]    
Share based compensation, shares authorized under significant ranges of outstanding stock option plans in period [Abstract]    
Warrants outstanding (in shares) | shares 27,989,723 32,502,790
Weighted-average exercise price of warrants outstanding (in dollars per share) 0.68 0.68
Range $0.41 - 1.50 [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) $ 0.41  
Range of Exercise Prices, Upper Range (in dollars per share) $ 1.50  
Number of Options (in shares) | shares 4,317,533  
Weighted-Average Remaining Contractual Life 9 years 5 months 12 days  
Weighted-Average Exercise Price (in dollars per share) $ 0.44  
Number of Options Exercisable (in shares) | shares 1,586,461  
Weighted-Average Remaining Contractual Life 9 years 5 months 16 days  
Weighted-Average Exercise Price, Options Exercisable (in dollars per share) $ 0.44  
Range $1.51 - 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) 1.51  
Range of Exercise Prices, Upper Range (in dollars per share) $ 2.50  
Number of Options (in shares) | shares 8,669,296  
Weighted-Average Remaining Contractual Life 7 years 3 months 25 days  
Weighted-Average Exercise Price (in dollars per share) $ 2.26  
Number of Options Exercisable (in shares) | shares 6,835,946  
Weighted-Average Remaining Contractual Life 7 years 25 days  
Weighted-Average Exercise Price, Options Exercisable (in dollars per share) $ 2.22  
Range $2.51 - 4.00 [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) 2.51  
Range of Exercise Prices, Upper Range (in dollars per share) $ 4.00  
Number of Options (in shares) | shares 960,670  
Weighted-Average Remaining Contractual Life 6 years 7 months 20 days  
Weighted-Average Exercise Price (in dollars per share) $ 2.88  
Number of Options Exercisable (in shares) | shares 937,337  
Weighted-Average Remaining Contractual Life 6 years 7 months 10 days  
Weighted-Average Exercise Price, Options Exercisable (in dollars per share) $ 2.87  
Range $4.01 - 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) 4.01  
Range of Exercise Prices, Upper Range (in dollars per share) $ 32.55  
Number of Options (in shares) | shares 2,895,424  
Weighted-Average Remaining Contractual Life 5 years 8 months 8 days  
Weighted-Average Exercise Price (in dollars per share) $ 5.24  
Number of Options Exercisable (in shares) | shares 2,895,424  
Weighted-Average Remaining Contractual Life 5 years 8 months 8 days  
Weighted-Average Exercise Price, Options Exercisable (in dollars per share) $ 5.24  
XML 42 R31.htm IDEA: XBRL DOCUMENT v3.7.0.1
Fair Value Measurements (Details) - USD ($)
$ in Thousands
6 Months Ended
Jun. 30, 2017
Dec. 31, 2016
Fair value measurements by level for assets and liabilities measured at fair value on a recurring basis [Abstract]    
Increase in fair value of warrant liabilities $ 2,800  
Recurring [Member]    
Fair value measurements by level for assets and liabilities measured at fair value on a recurring basis [Abstract]    
Cash equivalents 53,485 $ 56,276
Warrant liabilities (6,567) (3,789)
Level I [Member] | Recurring [Member]    
Fair value measurements by level for assets and liabilities measured at fair value on a recurring basis [Abstract]    
Cash equivalents 53,485 56,276
Warrant liabilities 0 0
Level II [Member] | Recurring [Member]    
Fair value measurements by level for assets and liabilities measured at fair value on a recurring basis [Abstract]    
Cash equivalents 0 0
Warrant liabilities 0 0
Level III [Member] | Recurring [Member]    
Fair value measurements by level for assets and liabilities measured at fair value on a recurring basis [Abstract]    
Cash equivalents 0 0
Warrant liabilities $ (6,567) $ (3,789)
XML 43 R32.htm IDEA: XBRL DOCUMENT v3.7.0.1
Liquidity and Capital Resources (Details) - USD ($)
2 Months Ended 6 Months Ended
Jul. 28, 2017
Jul. 27, 2017
Sep. 30, 2017
Jun. 30, 2017
Jun. 30, 2016
Dec. 31, 2016
Dec. 31, 2015
Estimated Projected Expenditure [Line Items]              
Cash and cash equivalents       $ 54,972,846 $ 55,913,199 $ 56,959,485 $ 22,261,372
Debt instrument, repayment of principal and unpaid interest       2,427,362 $ 0    
Currently projected expenditures for clinical programs       35,600,000      
NantCell, Inc [Member]              
Estimated Projected Expenditure [Line Items]              
Purchase of common stock       $ 13,000,000      
NantCell, Inc [Member] | Subsequent Event [Member]              
Estimated Projected Expenditure [Line Items]              
Purchase of common stock   $ 13,000,000          
Maturity date of amended loan servicing agreement   Aug. 01, 2018          
Hercules Technology Growth Capital, Inc. and Hercules Technology III, L.P. [Member]              
Estimated Projected Expenditure [Line Items]              
Maturity date of amended loan servicing agreement       Feb. 01, 2020      
Hercules Technology Growth Capital, Inc. and Hercules Technology III, L.P. [Member] | Subsequent Event [Member]              
Estimated Projected Expenditure [Line Items]              
Debt instrument, repayment of principal and unpaid interest $ 5,000,000 $ 5,000,000          
Hercules Technology Growth Capital, Inc. and Hercules Technology III, L.P. [Member] | Scenario, Forecast [Member]              
Estimated Projected Expenditure [Line Items]              
Debt instrument, repayment of principal and unpaid interest     $ 5,000,000        
Aldoxorubicin [Member]              
Estimated Projected Expenditure [Line Items]              
Currently projected expenditures for clinical programs       $ 4,700,000      
Other Programs [Member]              
Estimated Projected Expenditure [Line Items]              
Currently projected expenditures for clinical programs       3,700,000      
General Operation [Member]              
Estimated Projected Expenditure [Line Items]              
Currently projected expenditures for clinical programs       1,100,000      
Other General and Administrative Expenses [Member]              
Estimated Projected Expenditure [Line Items]              
Currently projected expenditures for clinical programs       9,400,000      
Interest and Term Loan Payment [Member]              
Estimated Projected Expenditure [Line Items]              
Currently projected expenditures for clinical programs       $ 16,600,000      
XML 44 R33.htm IDEA: XBRL DOCUMENT v3.7.0.1
Equity Transactions (Details) - shares
3 Months Ended
May 02, 2017
Jun. 30, 2017
Mar. 31, 2017
Class of Stock [Line Items]      
Authorized but unissued shares of common stock (in shares)   10,400,000  
Common stock shares issued from exercise of warrants (in shares)   4,404,494  
Issuance of common stock (in shares) 30,000,000    
Common Stock [Member]      
Class of Stock [Line Items]      
Number of preferred shares converted (in shares)     7,400,000
Series B Convertible Preferred Stock [Member]      
Class of Stock [Line Items]      
Number of preferred shares converted (in shares)     3,108
XML 45 R34.htm IDEA: XBRL DOCUMENT v3.7.0.1
Income Taxes (Details) - USD ($)
$ in Millions
6 Months Ended
Jun. 30, 2017
Dec. 31, 2016
Earliest Tax Year [Member]    
Operating Loss Carryforwards [Line Items]    
Expiration date Dec. 31, 2017  
Latest Tax Year [Member]    
Operating Loss Carryforwards [Line Items]    
Expiration date Dec. 31, 2036  
Federal [Member]    
Operating Loss Carryforwards [Line Items]    
Operating loss carryforwards   $ 339.0
Federal [Member] | Unrestricted [Member]    
Operating Loss Carryforwards [Line Items]    
Operating loss carryforwards   152.0
State [Member]    
Operating Loss Carryforwards [Line Items]    
Operating loss carryforwards   224.0
State [Member] | Unrestricted [Member]    
Operating Loss Carryforwards [Line Items]    
Operating loss carryforwards   $ 145.0
XML 46 R35.htm IDEA: XBRL DOCUMENT v3.7.0.1
Commitments and contingencies (Details)
$ in Millions
6 Months Ended
Jun. 30, 2017
USD ($)
Complaint
Loss Contingencies [Line Items]  
Amount of milestone payment payable $ 6.0
Potential future milestone payments on each additional final marketing approval $ 1.0
Number of competing derivative complaints | Complaint 2
Litigation settlement $ 0.7
NantCell, Inc [Member]  
Loss Contingencies [Line Items]  
Purchase of common stock 13.0
Obligation payable $ 0.6
XML 47 R36.htm IDEA: XBRL DOCUMENT v3.7.0.1
Subsequent Events (Details) - USD ($)
2 Months Ended 6 Months Ended
Jul. 28, 2017
Jul. 27, 2017
Sep. 30, 2017
Jun. 30, 2017
Jun. 30, 2016
Feb. 05, 2016
Subsequent Event [Line Items]            
Debt instrument, repayment of principal and unpaid interest       $ 2,427,362 $ 0  
Hercules Technology Growth Capital, Inc. and Hercules Technology III, L.P. [Member]            
Subsequent Event [Line Items]            
Warrants to purchase shares of common stock (in shares)           630,000
Warrants exercise price (in dollars per share)           $ 2.05
Hercules Technology Growth Capital, Inc. and Hercules Technology III, L.P. [Member] | Scenario, Forecast [Member]            
Subsequent Event [Line Items]            
Debt instrument, repayment of principal and unpaid interest     $ 5,000,000      
NantCell, Inc [Member]            
Subsequent Event [Line Items]            
Purchase of common stock       $ 13,000,000    
Subsequent Event [Member] | Hercules Technology Growth Capital, Inc. and Hercules Technology III, L.P. [Member]            
Subsequent Event [Line Items]            
Debt instrument, repayment of principal and unpaid interest $ 5,000,000 $ 5,000,000        
Prepayment charge $ 100,000          
Percentage of stock issuable upon exercise of the warrants   80.00%        
Number of days to calculate volume-weighted average price of common stock   30 days        
Subsequent Event [Member] | NantCell, Inc [Member]            
Subsequent Event [Line Items]            
Warrants exercise price (in dollars per share)   $ 1.10        
Purchase of common stock   $ 13,000,000        
Common stock, share price (in dollars per share)   $ 1.10        
Percentage of common stock premium at market price   92.00%        
Subsequent Event [Member] | NantCell, Inc [Member] | Maximum [Member]            
Subsequent Event [Line Items]            
Warrants to purchase shares of common stock (in shares)   3,000,000        
Milestone payment received   $ 343,000,000        
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