drugset / Trial / NCT02367872

Phase I Open-label Study to Evaluate Pharmacokinetics of TAK-272 in Participants With Renal or Hepatic Impairment

NCT02367872

Phase 1 Completed 48 enrolled Takeda
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to examine the effects of renal and hepatic impairment on TAK-272 pharmacokinetics with a single oral administration of TAK-272 in participants with renal or hepatic impairment.

Timeline

Start
2015-03
Primary completion
2016-06
Completion
2016-06

Drugs

EvaluationDrugModalityDoseRoute
Subject imarikiren Small molecule 40 mg Oral