drugset / Trial / NCT03048448

Pharmacokinetics of Fevipiprant (QAW039) in Patients With Hepatic Impairment Compared to Matched Healthy Subjects

NCT03048448

Phase 1 Completed 42 enrolled Novartis Pharmaceuticals
Non-randomizedParallel-groupOpen-labelOther

Summary

This study will characterize the pharmacokinetics (PK) of QAW039 after a single oral dose of QAW039 in patients with hepatic impairment compared to healthy matched control subjects.

Timeline

Start
2017-05-31
Primary completion
2019-04-22
Completion
2019-04-22

Drugs

EvaluationDrugModalityDoseRoute
Subject fevipiprant Small molecule 450 mg Oral

Indications

No indication recorded.