drugset / Trial / NCT01636778

Japanese Phase II Study of SB-497115-GR in Hepatitis C Virus Infected Patients

NCT01636778 ↗

Phase 2 Completed 45 enrolled GlaxoSmithKline
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to assess the ability of SB-497115-GR to raise platelet counts in thrombocytopenic patients with hepatitis C virus (HCV) infection (platelet count \<80,000 /μL, suggestive of compensated cirrhosis) to a level desirable to initiate antiviral therapy and to assess the ability of SB-497115-GR to maintain platelet counts at a level sufficient to minimise dose reductions of pegylated interferon (Peg-IFN) and ribavirin (RBV) therapy with the expectation that a lower rate of Peg-IFN dose reduction and omission will translate to a higher rate of sustained viral response.

Timeline

Start
2012-07
Primary completion
2014-05
Completion
2014-11

Drugs

EvaluationDrugModalityDoseRoute
Subject SB-497115-GR Unknown 12.5 mg —
Subject SB-497115-GR Unknown 25 mg —