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A Study of Orally Administered Pimodivir in Adult Participants With Renal Impairment

Kidney Failure, Chronic Clinical Trial

Official title:
A Phase 1, Open-label, Single-dose, Parallel-group Study to Evaluate the Effect of Renal Impairment on the Pharmacokinetics of Pimodivir in Adult Subjects

Clinical Trial Summary

The purpose of this study is to evaluate the pharmacokinetics (PK) of pimodivir after a single oral dose of 600 milligrams (mg) in adult participants with severe renal impairment who are not on dialysis and in adult participants with end-stage renal disease (ESRD) who are not yet on dialysis compared to adult participants with normal renal function (Part A). Optionally, to evaluate the PK in adult participants with mild and/or moderate renal impairment compared to adult participants with normal renal function (Part B).

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03947814
Study type Interventional
Source Janssen-Cilag International NV
Contact
Status Terminated
Phase Phase 1
Start date July 2, 2019
Completion date September 9, 2020
View Details
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