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Collaboration and Licensing Revenue
6 Months Ended
Jun. 30, 2016
Organization, Consolidation and Presentation of Financial Statements [Abstract]  
Collaboration and Licensing Revenue
Collaboration and Licensing Revenue
The Company generates revenue through contractual agreements with collaborators (known as exclusive channel collaborations, "ECC" or "ECCs") and licensing agreements whereby the collaborators or the licensees obtain exclusive access to the Company's proprietary technologies for use in the research, development and commercialization of products and/or treatments in a contractually specified field of use. Upfront and milestone payments are typically deferred and recognized over the expected life of the Company's technology platform using a straight-line approach. The Company recognizes the reimbursement payments received for research and development services in the period in which the services are performed and collection is reasonably assured. The following tables summarize the amounts recorded as revenue in the consolidated statements of operations for each significant collaboration or licensing agreement for the three and six months ended June 30, 2016 and 2015.
 
Three Months Ended June 30, 2016
 
Revenue Recognized From
 
Total
 
Upfront and Milestone Payments
 
Research and Development Services
 
ZIOPHARM Oncology, Inc.
$
922

 
$
6,048

 
$
6,970

Oragenics, Inc.
261

 
246

 
507

Fibrocell Science, Inc.
605

 
789

 
1,394

Genopaver, LLC
68

 
1,569

 
1,637

S & I Ophthalmic, LLC

 
2,358

 
2,358

OvaXon, LLC

 
808

 
808

Intrexon Energy Partners, LLC
625

 
3,587

 
4,212

Persea Bio, LLC
125

 
206

 
331

Ares Trading S.A.
1,597

 
621

 
2,218

Thrive Agrobiotics, Inc.
46

 
404

 
450

Intrexon Energy Partners II, LLC
500

 
394

 
894

Exotech Bio, Inc.
139

 

 
139

Relieve Genetics, Inc.
120

 
230

 
350

Intrexon T1D Partners, LLC
278

 
32

 
310

Other
2,769

 
2,134

 
4,903

Total
$
8,055

 
$
19,426

 
$
27,481

 
Three Months Ended June 30, 2015
 
Revenue Recognized From
 
Total
 
Upfront and Milestone Payments
 
Research and Development Services
 
ZIOPHARM Oncology, Inc.
$
644

 
$
4,606

 
$
5,250

Oragenics, Inc.
307

 
68

 
375

Fibrocell Science, Inc.
448

 
1,470

 
1,918

Genopaver, LLC
68

 
867

 
935

S & I Ophthalmic, LLC

 
890

 
890

OvaXon, LLC

 
662

 
662

Intrexon Energy Partners, LLC
625

 
2,731

 
3,356

Persea Bio, LLC
125

 
141

 
266

Ares Trading S.A.
739

 

 
739

Other
747

 
2,043

 
2,790

Total
$
3,703

 
$
13,478

 
$
17,181

 
Six Months Ended June 30, 2016
 
Revenue Recognized From
 
Total
 
Upfront and Milestone Payments
 
Research and Development Services
 
ZIOPHARM Oncology, Inc.
$
1,844

 
$
12,107

 
$
13,951

Oragenics, Inc.
524

 
789

 
1,313

Fibrocell Science, Inc.
1,210

 
2,041

 
3,251

Genopaver, LLC
137

 
3,078

 
3,215

S & I Ophthalmic, LLC

 
3,544

 
3,544

OvaXon, LLC

 
1,502

 
1,502

Intrexon Energy Partners, LLC
1,250

 
6,950

 
8,200

Persea Bio, LLC
250

 
405

 
655

Ares Trading S.A.
3,194

 
1,429

 
4,623

Thrive Agrobiotics, Inc.
92

 
792

 
884

Intrexon Energy Partners II, LLC
1,000

 
444

 
1,444

Exotech Bio, Inc.
139

 

 
139

Relieve Genetics, Inc.
120

 
230

 
350

Intrexon T1D Partners, LLC
278

 
32

 
310

Other
3,789

 
4,384

 
8,173

Total
$
13,827

 
$
37,727

 
$
51,554


 
Six Months Ended June 30, 2015
 
Revenue Recognized From
 
Total
 
Upfront and Milestone Payments
 
Research and Development Services
 
ZIOPHARM Oncology, Inc.
$
1,288

 
$
7,763

 
$
9,051

Oragenics, Inc.
569

 
76

 
645

Fibrocell Science, Inc.
896

 
3,183

 
4,079

Genopaver, LLC
137

 
1,467

 
1,604

S & I Ophthalmic, LLC

 
1,645

 
1,645

OvaXon, LLC

 
1,306

 
1,306

Intrexon Energy Partners, LLC
1,250

 
4,916

 
6,166

Persea Bio, LLC
250

 
256

 
506

Ares Trading S.A.
739

 

 
739

Other
1,605

 
4,618

 
6,223

Total
$
6,734

 
$
25,230

 
$
31,964


Except for the agreements discussed below, there have been no significant changes to arrangements with our collaborators and licensees in the six months ended June 30, 2016. See Note 5 in the Company's Annual Report on Form 10-K for the year ended December 31, 2015 for additional details of the Company's existing collaboration and licensing agreements.
Exotech Bio Collaboration
In March 2016, the Company entered into an ECC with Exotech Bio, Inc. ("Exotech Bio"), an affiliate of Harvest and a related party. Exotech Bio was formed for the purpose of entering into the ECC and developing and commercializing products using exosomes carrying a RNA payload designed to kill, suppress, or render immune-visible a cancer cell. Upon execution of the ECC, the Company received a technology access fee in the form of equity in Exotech Bio valued at $5,000 as upfront consideration. The Company is also entitled to up to $52,500 of potential payments for substantive and non-substantive development and commercial milestones for each product developed under the ECC. The Company receives reimbursement payments for research and development services provided pursuant to the ECC. Exotech Bio will pay the Company royalties as a percentage in the lower double-digits on the quarterly net sales of products developed under the ECC, as defined in the agreement. Exotech Bio is responsible for the development and commercialization of the product candidates. The term of the ECC commenced in March 2016 and continues until terminated pursuant to the ECC agreement. The ECC may be terminated by either party in the event of certain material breaches defined in the agreement and may be terminated voluntarily by Exotech Bio upon 90 days written notice to the Company.
Relieve Genetics Collaboration
In March 2016, the Company entered into an ECC with Relieve Genetics, Inc. ("Relieve Genetics"), an affiliate of Harvest and a related party. Relieve Genetics was formed for the purpose of entering into the ECC and developing and commercializing products using a viral vector expressing interleukin-10 for the treatment of chronic neuropathic pain resultant from cancer in humans. Upon execution of the ECC, the Company received a technology access fee in the form of equity in Relieve Genetics valued at $4,333 as upfront consideration. The Company is also entitled to up to $52,500 of potential payments for substantive and non-substantive development and commercial milestones for each product developed under the ECC. The Company receives reimbursement payments for research and development services provided pursuant to the ECC. Relieve Genetics will pay the Company royalties as a percentage in the lower double-digits on the quarterly net sales of products developed under the ECC, as defined in the agreement. Relieve Genetics is responsible for the development and commercialization of the product candidates. The term of the ECC commenced in March 2016 and continues until terminated pursuant to the ECC agreement. The ECC may be terminated by either party in the event of certain material breaches defined in the agreement and may be terminated voluntarily by Relieve Genetics upon 90 days written notice to the Company.
Intrexon T1D Partners Collaboration
In March 2016, the Company entered into an ECC with Intrexon T1D Partners, a related party. Pursuant to the ECC, Intrexon T1D Partners received an exclusive license to the Company's technology platform to develop and commercialize products to treat type 1 diabetes. Upon execution of the ECC, the Company received a technology access fee of $10,000 and is entitled to reimbursement of research and development services as provided for in the ECC agreement. The term of the ECC commenced in March 2016 and continues until March 2036; termination prior to that date may be initiated (i) by either party in the event of certain material breaches defined in the agreement or (ii) may be terminated Intrexon T1D Partners upon 90 days written notice to the Company.
AD Skincare Collaboration
In June 2016, the Company entered into an ECC with AD Skincare, Inc. ("AD Skincare"), an affiliate of Harvest and a related party. AD Skincare was formed for the purpose of entering into the ECC and developing an advanced topical delivery system to improve the efficacy of biologically active ingredients aimed at improving signs of aging human skin. Upon execution of the ECC, the Company received a technology access fee in the form of equity in AD Skincare valued at $4,333 as upfront consideration. The Company is also entitled to up to $2,000 of potential payments for substantive and non-substantive development milestones for each product developed under the ECC, as well as up to $17,000 in one-time commercial milestones. The Company receives reimbursement payments for research and development services provided pursuant to the ECC. AD Skincare will pay the Company royalties as a percentage in the low double-digits on the quarterly net sales of products developed under the ECC, as defined in the agreement. AD Skincare is responsible for the development and commercialization of the product candidates. The term of the ECC commenced in June 2016 and continues until terminated pursuant to the ECC agreement. The ECC may be terminated by either party in the event of certain material breaches defined in the agreement and may be terminated voluntarily by AD Skincare upon 90 days written notice to the Company.
ZIOPHARM Collaborations
In June 2016, the Company amended each of its two existing collaboration agreements with ZIOPHARM and as a result the rate of the royalty which the Company is entitled to receive on certain products commercialized pursuant to the agreements was reduced from 50% to 20%. As consideration for execution of the amendments, ZIOPHARM issued the Company 100,000 shares of ZIOPHARM's Series 1 Preferred Stock valued at $120,000. The Company allocated the consideration received to each ECC based on the cumulative value of upfront and milestone payments previously received pursuant to that ECC. Because the Company has remaining performance obligations under each of the ZIOPHARM ECCs, the Company recorded the initial fair value received as deferred revenue and will recognize this amount straight-line over the remaining performance period for each ZIOPHARM ECC. No other financially significant terms of the ZIOPHARM ECCs were changed as a result of the amendments. See Note 7 for additional discussion of the terms of the preferred stock and the accounting treatment.
Deferred Revenue
Deferred revenue primarily consists of consideration received for upfront and milestone payments in connection with the Company's collaborations and licensing agreements, prepayments for research and development services performed for collaborators and licensees, and prepayments for product and service revenues. Deferred revenue consists of the following:
 
June 30,
2016
 
December 31,
2015
Upfront and milestone payments
$
310,937

 
$
181,331

Prepaid research and development services
8,122

 
10,938

Prepaid product and service revenues
5,471

 
4,759

Other
709

 
701

Total
$
325,239

 
$
197,729

Current portion of deferred revenue
$
53,863

 
$
35,366

Long-term portion of deferred revenue
271,376

 
162,363

Total
$
325,239

 
$
197,729


The following table summarizes the remaining balance of deferred revenue associated with upfront and milestone payments for each significant collaboration and licensing agreement:
 
June 30,
2016
 
December 31,
2015
ZIOPHARM Oncology, Inc.
$
148,494

 
$
30,338

Oragenics, Inc.
8,289

 
8,813

Fibrocell Science, Inc.
20,235

 
21,445

Genopaver, LLC
2,113

 
2,250

Intrexon Energy Partners, LLC
19,375

 
20,625

Persea Bio, LLC
4,250

 
4,500

Ares Trading S.A.
50,373

 
53,567

Thrive Agrobiotics, Inc.
1,529

 
1,621

Intrexon Energy Partners II, LLC
16,833

 
17,833

Exotech Bio, Inc.
4,861

 

Relieve Genetics, Inc.
4,213

 

Intrexon T1D Partners, LLC
9,564

 

AD Skincare, Inc.
4,333

 

Other
16,475

 
20,339

Total
$
310,937

 
$
181,331