BARCELONA, Spain--(BUSINESS WIRE)--Apr 11, 2007 - New data
supporting the clinical development of telaprevir (VX-950), one of
the most advanced investigational oral protease inhibitors for the
treatment of hepatitis C virus (HCV) infection, will be presented
at the 42nd Annual Meeting of the European Association for the
Study of the Liver (EASL) in Barcelona this week. In total, nine
abstracts related to telaprevir have been accepted for presentation
at the EASL conference, including an abstract that describes
telaprevir activity against genotypes 2, 3 and 4 in vitro. A
late-breaker oral presentation will take place on Saturday, April
14 at 5:45 p.m. Central European Summer Time (11:45 a.m. Eastern
Daylight Time). Vertex Pharmaceuticals Incorporated (Nasdaq: VRTX)
is developing telaprevir in collaboration with Tibotec.
"Hepatitis C is a major global health problem with a significant
unmet medical need. Despite treatment advancements in the last 10
years, there is an urgent need for new therapeutic options that can
offer patients shorter course therapy and better efficacy," said
John Alam, M.D., Executive Vice President, Medicines Development,
and Chief Medical Officer of Vertex. "The data to be presented at
EASL demonstrate the recent progress made in our clinical
evaluation and understanding of telaprevir as a novel treatment for
hepatitis C, underscoring our commitment to evaluate telaprevir's
potential in important sub-populations, such as those with genotype
non-1 hepatitis C."
Telaprevir is one of the most advanced specifically targeted
antiviral therapies for HCV (STAT-C). STAT-Cs represent a new
approach to hepatitis C treatment by directly targeting the enzymes
the virus uses to replicate.
Oral Presentation: Telaprevir Demonstrates Potency Against
Genotype 2, 3 and 4 in vitro
Chao Lin, Ph.D., of Vertex, will present an abstract titled,
"Telaprevir (VX-950) is a Potent Inhibitor of H
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