drugset / Trial / NCT01265511

Study of SCY-635, Pegasys and Copegus in Hepatitis C

NCT01265511 ↗

Phase 2 Completed 10 enrolled Scynexis, Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study will examine the effectiveness of 28 days of triple combination therapy including SCY-635 with peginterferon alfa 2a and ribavirin in reducing serum HCV RNA levels. An additional 20 weeks of treatment with the currently approved standard of care will be offered to all participants. The Week 24 visit will be the last on-study visit. After the Week 24 visit, all subjects with undetectable HCV RNA will be given the option to continue treatment with standard of care for an additional 24 weeks (out to Week 48) under the care of their Principal Investigator.

Timeline

Start
2010-11
Primary completion
2011-10
Completion
2011-10

Drugs

EvaluationDrugModalityDoseRoute
Comparator Peginterferon alfa-2a Protein / enzyme biologic 180 ug —
Comparator Ribavirin Small molecule — Oral
Comparator SCY-635 Protein / enzyme biologic 300 mg Oral