drugset / Trial / NCT02808312

Pharmacokinetics and Pharmacodynamics of Cilofexor in Adults With Normal and Impaired Hepatic Function

NCT02808312

Phase 1 Completed 57 enrolled Gilead Sciences
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The primary objective of this study is to evaluate the single-dose pharmacokinetics of cilofexor in adults with impaired hepatic function relative to matched, healthy controls with normal hepatic function.

Timeline

Start
2016-07-13
Primary completion
2018-10-16
Completion
2018-10-16

Drugs

EvaluationDrugModalityDoseRoute
Subject Cilofexor Small molecule 10 mg Oral
Subject Cilofexor Small molecule 30 mg Oral