Clinical Trials Directory

Trials / Completed

CompletedNCT02039817

PK and PD Study of IDN-6556 in Subjects With Severe Renal Impairment and Matched Healthy Volunteers

An Open-Label Pharmacokinetic and Pharmacodynamic Study of a Single Dose of IDN-6556 in Subjects With Severe Renal Impairment and in Matched Healthy Volunteers

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
16 (actual)
Sponsor
Conatus Pharmaceuticals Inc. · Industry
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Accepted

Summary

This is an open-label, parallel-group study to compare the pharmacokinetics and pharmacodynamics of IDN-6556 following a single 50 mg oral dose of IDN-6556 in subjects with severe renal impairment and matched healthy volunteers with normal renal function.

Conditions

Interventions

TypeNameDescription
DRUGIDN-6556

Timeline

Start date
2014-01-01
Primary completion
2014-04-01
Completion
2014-04-01
First posted
2014-01-20
Last updated
2016-01-28
Results posted
2016-01-28

Locations

2 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT02039817. Inclusion in this directory is not an endorsement.

PK and PD Study of IDN-6556 in Subjects With Severe Renal Impairment and Matched Healthy Volunteers (NCT02039817) · Clinical Trials Directory