drugset / Trial / NCT02441829

Pharmacokinetics of Eleclazine in Adults With Normal and Impaired Renal Function

NCT02441829

Phase 1 Completed 55 enrolled Gilead Sciences
Non-randomizedParallel-groupOpen-labelTreatment

Summary

This study will evaluate the pharmacokinetics (PK), safety, and tolerability of a single oral dose of eleclazine and its metabolite, GS-623134, in participants with normal and impaired renal function. Participants in the healthy control group will be matched to participants with impaired renal function by age (± 5 years), gender, and body mass index (± 10%).

Timeline

Start
2015-05
Primary completion
2015-12
Completion
2015-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Eleclazine Small molecule 30 mg Oral

Indications