drugset / Trial / NCT06529796

Evaluation of the Pharmacokinetics and Safety of Inaxaplin in Participants With Mild or Moderate Hepatic Impairment

NCT06529796 ↗

Phase 1 Completed 36 enrolled Vertex Pharmaceuticals Incorporated
Non-randomizedParallel-groupOpen-labelBasic science

Summary

The purpose of this study is to evaluate the pharmacokinetics, safety and tolerability of Inaxaplin (IXP) in participants with mild or moderate hepatic impairment and in matched healthy participants.

Timeline

Start
2024-08-02
Primary completion
2024-12-20
Completion
2024-12-20

Drugs

EvaluationDrugModalityDoseRoute
Subject IXP Unknown — Oral