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Completed trials with posted results — search by concept, filter by the parameters that matter at the bedside.

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12,372 trials

Phase 3 N=50 Safety and Efficacy Study of the Combination Daclatasvir (60 mg), Sofosbuvir (400 mg) and Ribavirin (Weight-based Dosing) for 12 or 16 Weeks in Subjects With Genotype 3 Chronic HCV Infection With or Without Prior Treatment Experience and Advanced Fibrosis or Compensated Cirrhosis

Hepatitis C
Primary: Percent of Participants With a Sustained Virologic Response (SVR) at Follow-up Week 12 (SVR12) — 87.5; 92.3 percentage of participants
Bristol-Myers Squibb Results Jan 2017 10.0% serious AE View details