Clinical Trial

Study of Bemnifosbuvir/Ruzasvir as a Fixed-dose Combination in Subjects With Normal or Severely Impaired Renal or Hepatic Function

Completed Phase 1
View on ClinicalTrials.gov →
Summary
To Assess the Effect of Severe Hepatic or Renal Impairment on the Pharmacokinetics of Bemnifosbuvir/Ruzasvir After a Single Dose
Protocol Amendment History 1 change
critical Trial completed 2026-08-01
Trial Details
NCT Number NCT06911320
Lead Sponsor Atea Pharmaceuticals, Inc.
Conditions Healthy Volunteer Study, Hepatic Impairment, Renal Impairment
Enrollment 28 participants
Start Date 2025-04-09
Primary Completion 2026-04-30 (estimated)
Study Completion 2026-04-30 (estimated)
Updated on ClinicalTrials.gov 2026-07-31