drugset / Trial / NCT03555539

Study of Danicopan in Participants With Hepatic Impairment

NCT03555539

Non-randomizedParallel-groupOpen-labelBasic science

Summary

The purpose of this study was to evaluate the safety, tolerability, and pharmacokinetics (PK) of ACH-0144471 (danicopan) in participants with hepatic impairment (HI) as compared to healthy matched participants.

Timeline

Start
2018-05-01
Primary completion
2018-09-21
Completion
2018-09-21

Drugs

EvaluationDrugModalityDoseRoute
Subject Danicopan Small molecule 200 mg Oral

Indications

No indication recorded.