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.