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Trials / Completed

CompletedNCT04208386

A Study to Evaluate the Effect of Hepatic Impairment on JNJ-73763989

A Phase 1, Single-Dose, Open-Label, Parallel-Group Study to Evaluate the Effect of Hepatic Impairment on the Pharmacokinetics of JNJ-73763989

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
16 (actual)
Sponsor
Janssen Sciences Ireland UC · Industry
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Accepted

Summary

The purpose of the study is to evaluate the single-dose pharmacokinetic (PK) of JNJ-73763976 and JNJ-73763924 following a subcutaneous (SC) injection of JNJ-73763989 (JNJ-3989) in participants with liver cirrhosis and various degrees of impaired hepatic function when compared with healthy participants with normal hepatic function and no liver cirrhosis.

Conditions

Interventions

TypeNameDescription
DRUGJNJ-73763989JNJ-73763989 will be administered SC under fasted condition.

Timeline

Start date
2020-01-08
Primary completion
2020-07-20
Completion
2020-07-20
First posted
2019-12-23
Last updated
2020-09-30

Locations

1 site across 1 country: Germany

Regulatory

Source: ClinicalTrials.gov record NCT04208386. Inclusion in this directory is not an endorsement.

A Study to Evaluate the Effect of Hepatic Impairment on JNJ-73763989 (NCT04208386) · Clinical Trials Directory