drugset / Trial / NCT03913000

A Study to Evaluate ID-085 in People With Mild, Moderate, and Severe Kidney Disease

NCT03913000 ↗

Phase 1 Completed 32 enrolled Idorsia Pharmaceuticals Ltd.
SequentialOpen-labelOther

Summary

The primary objective of this study is to evaluate the pharmacokinetics (PK), tolerabilty and safety of a single dose of ID-085 in subjects with mild, moderate, and severe renal function impairment compared to healthy subjects

Timeline

Start
2019-04-29
Primary completion
2019-08-22
Completion
2019-08-22

Drugs

EvaluationDrugModalityDoseRoute
Subject ID-085 Unknown 200 mg Oral