Clinical Trials Directory

Trials / Completed

CompletedNCT02961660

A Study to Evaluate the Effect of Severe Renal Impairment on the Single-dose Pharmacokinetics of Odalasvir

An Open-label Study to Evaluate the Effect of Severe Renal Impairment on the Single-dose Pharmacokinetics of Odalasvir

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
16 (actual)
Sponsor
Janssen Research & Development, LLC · Industry
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Accepted

Summary

The main purpose of this study is to evaluate the pharmacokinetics (PK) of a single oral dose of odalasvir (ODV) in participants with severe renal impairment and compare with the PK in matched participants with normal renal function.

Conditions

Interventions

TypeNameDescription
DRUGOdalasvirParticipants will receive odalasvir 25 mg tablet, orally.

Timeline

Start date
2016-11-09
Primary completion
2018-04-09
Completion
2018-04-09
First posted
2016-11-11
Last updated
2025-02-03

Locations

2 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT02961660. Inclusion in this directory is not an endorsement.