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[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
BIO Advocacy ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
BIO Advocates on Revenue Recognition ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Collaborative Arrangements ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
BIO Revenue Recognition Study ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object]
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],Affymax/Takeda Collaboration
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],Accounting for Collaboration
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],Impact of Amendment
[object Object]
Regeneron Collaboration Agreements * 50% repayment from profits  ** plus $475MM of research funding over 5 years Oncology Eye Disease Antibodies sanofi-aventis Bayer HealthCare sanofi-aventis Upfront/milestone payments $130MM $95MM $85MM Development costs paid by partner * 100% ~50% ~100%** Profit split – Regeneron share US 50% 100% 50% Japan ~35% royalty 50% 35-45% ROW 50% 50% 35-45% Milestones remaining Regulatory $400MM $90MM – Sales – $135MM $250MM
Sanofi-Aventis Antibody Collaboration   ,[object Object],[object Object],[object Object]
[object Object]
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],Adolor/Pfizer Collaboration
Recent Benchmark Example  Pain Compounds in Phase IIa Adolor/Pfizer Targacept/GSK Glenmark/Lilly Transaction Date December 4, 2007 July 27, 2007 October 30, 2007 Pain Target Delta Opoid Receptor Neuronal Nicotinic Receptor Transient Receptor Potential Vanilloid Sub-family 1 (TRPV1) Lead Compound ADL5859 TC-2696 GRC 6211 Upfront Payment $30 Million + $1.9 Million reimbursement for Phase 2a studies $20 Million Plus $15 Million in Equity $45 Million ,[object Object],[object Object],[object Object],[object Object],[object Object],Not Disclosed Not Disclosed Not Disclosed ____ $232.5 MM Not Disclosed Not Disclosed Not Disclosed $1.5 B Not Disclosed Not Disclosed Not Disclosed $215 MM Back End US – 40/60 Profit Split ROW Royalties Undisclosed Double Digit Royalty ~15% Royalty in the Territory Territory Worldwide Worldwide North America, Europe, and Japan Cost Sharing 40/60 US 100% Pfizer in ROW Targacept to fund through Phase 2 POC. Then 100% GSK if they opt to take the compound 100% Lilly in Territory - no mention of access to Lilly trial data Co-promote Option Yes – US Specialty Yes – US Specialty for first two compounds Yes – US
[object Object],[object Object],[object Object],Deal Structure for Revenue Recognition
Accounting for Upfront Payments ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Best Practices: What Biotechs Can Do ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Best Practices: What Biotechs Can Do ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Best Practices: What Biotechs Can Do ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Best Practices: What Biotechs Can Do ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
BIO Study:  Recommendations for FASB & SEC ,[object Object],[object Object],[object Object]
Advocacy ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Discussion & Questions  ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]

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Revenue Recognition Guidance for Biotech Collaborations

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  • 12. Regeneron Collaboration Agreements * 50% repayment from profits ** plus $475MM of research funding over 5 years Oncology Eye Disease Antibodies sanofi-aventis Bayer HealthCare sanofi-aventis Upfront/milestone payments $130MM $95MM $85MM Development costs paid by partner * 100% ~50% ~100%** Profit split – Regeneron share US 50% 100% 50% Japan ~35% royalty 50% 35-45% ROW 50% 50% 35-45% Milestones remaining Regulatory $400MM $90MM – Sales – $135MM $250MM
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