HomeTrialNCT06911320
🔬NCT06911320Phase 1RECRUITING

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

Study Summary

To Assess the Effect of Severe Hepatic or Renal Impairment on the Pharmacokinetics of Bemnifosbuvir/Ruzasvir After a Single Dose

View on ClinicalTrials.gov ↗
Study Details
Enrollment28 participants
Primary Completion
Lead SponsorAtea Pharmaceuticals, Inc.
Data Retrieved2026-04-11 02:55:17.105140+00:00
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