Overview

Safety, PK and Efficacy of 15 Days of SCY-635 Treatment in Hepatitis C Patients

Status:
Completed
Trial end date:
2009-01-01
Target enrollment:
Participant gender:
Summary
This study will examine the effectiveness of 15 days of therapy with SCY-635 in reducing hepatitis C virus (HCV) RNA levels.
Phase:
Phase 1
Details
Lead Sponsor:
Scynexis, Inc.