drugset / Trial / NCT01290965

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

NCT01290965 ↗

Phase 1 Completed 57 enrolled Scynexis, Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study will examine the effectiveness of 15 days of therapy with SCY-635 in reducing hepatitis C virus (HCV) RNA levels.

Timeline

Start
2007-04
Primary completion
2008-12
Completion
2009-01

Drugs

EvaluationDrugModalityDoseRoute
Comparator SCY-635 Protein / enzyme biologic 30 mg Oral
Comparator SCY-635 Protein / enzyme biologic 100 mg Oral
Comparator SCY-635 Protein / enzyme biologic 200 mg Oral
Comparator SCY-635 Protein / enzyme biologic 300 mg Oral