Jun 29 2012
Medivir AB (OMX:MVIR), the research-based pharmaceutical company focused
on the development of high-value treatments for infectious diseases,
announces that a phase II combination study with the investigational
compound TMC435 and Bristol-Myers Squibb's investigational compound
daclatasvir will start in July. This study is part of the clinical
collaboration agreement between Janssen R&D Ireland and Bristol-Myers
Squibb Company (NYSE:BMY) announced on 2 December 2011 and on 18 April
2012.
TMC435 and daclatasvir (BMS-790052)
TMC435, a once daily potent NS3/4A protease inhibitor (PI) in phase III
clinical development for the treatment of chronic genotype-1 hepatitis C
virus (HCV) infection, will be investigated in an interferon free phase
II trial in combination with Bristol-Myers Squibb´s investigational NS5A
replication complex inhibitor, daclatasvir (BMS-790052), also in phase
III development.
The purpose of this study is to assess the efficacy and safety of TMC435
and daclatasvir in combination with or without Ribavirin in chronic
genotype-1 hepatitis C infected patients who are treatment-naive or null
responders to previous Peginterferon alfa/Ribavirin therapy.
Study design
In this open label phase II study the potential to achieve sustained
viral response (SVR), 12 (SVR12) and 24 (SVR24) weeks post treatment in
treatment-naïve and null responder patients infected with HCV genotype
1a and 1b will be evaluated. Patients with advanced liver disease
(F3/F4) will be allowed up to approx. 35% of the total treated
population.
Cohort one and two will include patients with genotype 1b where TMC435
and daclatasvir will be dosed with or without Ribavirin for 12 weeks
with a 36 weeks follow-up or for 24 weeks with a 24 weeks follow-up.
Cohort three and four will include patients with genotype 1a where
TMC435, daclatasvir and Ribavirin will be dosed for 12 or 24 weeks with
a 24 weeks post treatment follow-up.