drugset / Trial / NCT01651767

Study in HCV-Infected Patients to Determine the Safety, Tolerability, Pharmacokinetics and Antiviral Activity of JNJ-47910382

NCT01651767 ↗

Phase 1 Terminated 11 enrolled Janssen R&D Ireland
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to determine the safety, tolerability, pharmacokinetics (what the body does to the medication) and antiviral activity of JNJ-47910382 when administered in different dosing regimens in Caucasian genotype-1 chronic HCV-infected patients.

Timeline

Start
2012-08
Primary completion
2013-06
Completion
2013-06

Outcome

Outcome not reported

Stopped: “Because of many competing trials using the same mechanism of action, but being further advanced in development”

Drugs

EvaluationDrugModalityDoseRoute
Subject JNJ-47910382 Unknown 30 mg Oral
Subject JNJ-47910382 Unknown 90 mg Oral
Subject JNJ-47910382 Unknown 300 mg Oral
Subject JNJ-47910382 Unknown 400 mg Oral
Subject JNJ-47910382 Unknown 450 mg Oral