Hepatitis C Infection Clinical Trial
Official title:
A Bioequivalence Study of the 90-mg Daclatasvir Tablet Relative to the 3 × 30-mg Daclatasvir Phase 3 Tablets, and Relative Bioavailability Studies of Chewable Pediatric Tablets of Daclatasvir and Asunaprevir in Healthy Adult Subjects
Grps 1, 2, 3 "This study will be testing the performance of ASV and DCV pediatric chewable
tablets.
Grp #4 The purpose of this group is to support the marketing authorization of a DCV 90-mg
tablet
n/a
Allocation: Randomized, Endpoint Classification: Bio-equivalence Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Basic Science
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