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                Below 
                  is an excerpt from a press release issued by the 2 companies 
                  describing their forthcoming joint work. 
              
                Bristol-Myers 
                  Squibb and Pharmasset Enter into a Clinical Collaboration Agreement 
                  for Proof of Concept Combination Study in Patients Chronically 
                  Infected with Hepatitis C 
                  
                  
                     
                      |  | Study 
                        is the first cross-company collaboration combining two 
                        oral, direct-acting antivirals |   
                      |  | Study 
                        to evaluate the combination with and without ribavirin 
                        in treatment-naive patients |  
                New 
                  York, N.Y. and Princeton, N.J. -- January 10, 2011 -- Bristol-Myers 
                  Squibb Company (NYSE:BMY) and Pharmasset (NASDAQ: VRUS) announced 
                  today that the companies have entered into a clinical collaboration 
                  agreement to evaluate the utility of BMS-790052, Bristol-Myers 
                  Squibb's NS5A replication complex inhibitor, in combination 
                  with PSI-7977, Pharmasset's nucleotide polymerase inhibitor, 
                  for the treatment of chronic hepatitis C virus (HCV). 
                This proof of concept study will evaluate the potential to achieve 
                  sustained viral response 24 weeks post treatment with an oral, 
                  once-daily treatment regimen in patients across HCV genotypes. 
                  Specifically, the study will assess the safety, pharmacokinetics 
                  and pharmacodynamics of BMS-790052 in combination with PSI-7977, 
                  with and without ribavirin, in treatment-naive patients chronically 
                  infected with HCV genotypes 1, 2, and 3. The study is planned 
                  to start in the first half of 2011. This collaboration represents 
                  the first cross-company collaboration combining two oral agents 
                  to address a significant unmet medical need in the treatment 
                  of HCV.
 
                "Bristol-Myers Squibb is committed to the goal of helping 
                  patients prevail over hepatitis C by investigating multiple 
                  therapeutic platforms," said Brian Daniels, senior vice 
                  president, Development. "We are pleased to partner with 
                  Pharmasset on this important study to advance the scientific 
                  understanding of the potential for an all-oral regimen to treat 
                  hepatitis C. Conducting this study highlights Bristol-Myers 
                  Squibb's ability to collaborate with other companies to develop 
                  innovative combination therapies in areas of high unmet need."
 
 
 
                "We 
                  are excited to be working with Bristol-Myers Squibb and to be 
                  investigating PSI-7977 with a different class of direct acting 
                  antivirals," stated Michelle Berrey, MD, MPH, Chief Medical 
                  Officer. "This collaboration represents one of many approaches 
                  we are pursuing with our portfolio of nucleoside/tide analogs 
                  that include both interferon free and interferon-sparing regimens. 
                  We believe the development of an all oral treatment regimen 
                  represents an important evolution in the treatment of HCV." 
                BMS-790052 is an investigational oral hepatitis C NS5A replication 
                  complex inhibitor. NS5A is one of the essential components for 
                  HCV replication. BMS-790052 is one of several molecules Bristol-Myers 
                  Squibb is studying for the potential treatment of chronic hepatitis 
                  C. The portfolio of investigational compounds, which also includes 
                  a novel pegylated interferon lambda, fits into the company's 
                  overall R&D focus on diseases where there is major unmet 
                  medical need.
 
 
 
                PSI-7977 is a uracil nucleotide analog inhibitor of the NS5B 
                  polymerase being developed for the treatment of chronic HCV 
                  infection. Nucleotide analog polymerase inhibitors work by acting 
                  as alternative substrates that block the synthesis of HCV RNA, 
                  which is essential for the virus to replicate. PSI-7977 has 
                  been studied in combination with peginterferon and ribavirin 
                  for up to 12 weeks in genotype 1, 2 or 3 patients and is currently 
                  in two Phase 2b studies, one of which is investigating an interferon 
                  sparing regimen in genotype 2 or 3 patients. PSI-7977 is also 
                  being investigated in a 14-day combination study with PSI-938, 
                  a guanine nucleotide analog.
 
                About Bristol-Myers Squibb
 
 
 
                Bristol-Myers 
                  Squibb is a global biopharmaceutical company whose mission is 
                  to discover, develop and deliver innovative medicines that help 
                  patients prevail over serious diseases. For more information, 
                  please visit http://www.bms.com 
                  or follow us on Twitter at http://twitter.com/bmsnews. 
                  
 
 
                Pharmasset is a clinical-stage pharmaceutical company committed 
                  to discovering, developing, and commercializing novel drugs 
                  to treat viral infections. Pharmasset's primary focus is on 
                  the development of oral therapeutics for the treatment of hepatitis 
                  C virus (HCV). Our research and development efforts focus on 
                  nucleoside/tide analogs, a class of compounds which act as alternative 
                  substrates for the viral polymerase, thus inhibiting viral replication. 
                  We currently have four clinical-stage product candidates. RG7128, 
                  a cytosine nucleoside analog for chronic HCV infection, is in 
                  two Phase 2b clinical studies in combination with Pegasys plus 
                  Copegus and is also in the INFORM studies, the first series 
                  of studies designed to assess the potential of combinations 
                  of small molecules without Pegasys and Copegus to treat chronic 
                  HCV. These clinical studies are being conducted through a strategic 
                  collaboration with Roche. Our other clinical stage HCV candidates 
                  include PSI-7977, an unpartnered uracil nucleotide analog that 
                  is in two Phase 2b studies in patients with HCV genotypes 1, 
                  2, or 3, and PSI-938, an unpartnered guanine nucleotide analog 
                  which recently completed a 14-day monotherapy study and has 
                  recently initiated a 14-day combination study with PSI-7977. 
                  We also have in our pipeline an additional purine nucleotide 
                  analog, PSI-661, in advanced preclinical development. For more 
                  information visit www.pharmasset.com.
 
              
                1/14/11 SourceBristol-Myers 
                  Squibb and Pharmasset. Bristol-Myers Squibb and Pharmasset Enter 
                  into a Clinical Collaboration Agreement for Proof of Concept 
                  Combination Study in Patients Chronically Infected with Hepatitis 
                  C. Press release. January 10, 2011.
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