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Medivir Notes That Partner Tibotec Announced Week 24 Interim Results From Phase 2b TMC435 PILLAR Study to be Presented as a Late-Breaker at AASLD
Date:11/1/2010

n ongoing Japanese phase 2b study in 92 genotype-1 treatment-naive patients. It evaluates once daily treatment of TMC435 with different doses and durations given in addition to standard of care treatment, consisting of ribavirin and pegIFNalpha-2A.

Opera-2 (TMC435-C202)

TMC435-C202 is a completed phase 2a study in treatment-naive genotype 2 to 6 HCV patients. It is a once daily treatment of TMC435 during seven days, at 200 mg. Subsequently, patients could continue with Standard of Care treatment consisting of pegylated interferon and ribavirin upon agreement with the study doctor.

For more information about Medivir, please contact: Medivir (http://www.medivir.se) Rein Piir, CFO & VP Investor Relations Office: +46-8-546-831-23 Mobile: +46-708-537-292 M:Communications: Medivir@mcomgroup.com Europe: Mary-Jane Elliott / Emma Thompson / Amber Bielecka: +44(0)20-7920-2330 USA: Jason Marshall: +1-212-897-5497 For enquiries about the above briefings, please contact: Lindsey Neville at M:Communications on +44(0)20-7920-2333 or Jason Marshall on +1-212-889-4350 or email Neville@mcomgroup.com
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