A Study to Evaluate the Effect of Hepatic Insufficiency on the Pharmacokinetics (PK) of ACP-196

PHASE1CompletedINTERVENTIONAL
Enrollment

18

Participants

Timeline

Start Date

October 21, 2014

Primary Completion Date

February 2, 2015

Study Completion Date

February 2, 2015

Conditions
Hepatic Insufficiency
Interventions
DRUG

ACP-196

All study participants will receive a single oral dose of 50 mg ACP-196 (2 x 25 mg capsules) on Day 1 of the study.

Trial Locations (3)

32809

Research Site, Orlando

33136

Research Site, Miami

37920

Research Site, Knoxville

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Acerta Pharma BV

INDUSTRY

NCT04867941 - A Study to Evaluate the Effect of Hepatic Insufficiency on the Pharmacokinetics (PK) of ACP-196 | Biotech Hunter | Biotech Hunter