drugset / Trial / NCT07457190

Pharmacokinetic Study of Buagafuran Capsules in Participants With Hepatic Impairment and Normal Hepatic Function

NCT07457190

Phase 1 Not yet recruiting 24 enrolled Beijing Union Pharmaceutical Factory Ltd
Non-randomizedParallel-groupOpen-labelOther

Summary

This study adopts a non-randomized, open label, parallel, single-dose design to evaluate the safety and pharmacokinetic characteristics of Buagafuran capsules in participants with hepatic impairment.

Timeline

Start
2026-03
Primary completion
2026-08
Completion
2026-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Buagafuran Unknown 30 mg