drugset / Trial / NCT02662712

A Study of Orally Administered JNJ-56136379 to Evaluate Safety, Tolerability and Pharmacokinetics After Single Ascending Doses and One Multiple Dose Regimen in Healthy Participants (Part I), and After Multiple Dose Regimens in Participants With Chronic Hepatitis B (Part II)

NCT02662712

Phase 1 Completed 87 enrolled Janssen Sciences Ireland UC
RandomizedParallel-groupTriple-blindOther

Summary

The purpose of this study is to evaluate pharmacokinetics and safety data including serious and other adverse events, physical examinations, vital signs, 12-lead electrocardiograms (ECGs) and clinical laboratory results (including biochemistry, hematology, and urine).

Timeline

Start
2015-12-17
Primary completion
2018-06-29
Completion
2018-06-29

Drugs

EvaluationDrugModalityDoseRoute
Subject bersacapavir Other / unclassified 25 mg Oral
Subject bersacapavir Other / unclassified 75 mg Oral
Subject bersacapavir Other / unclassified 100 mg Oral
Subject bersacapavir Other / unclassified 150 mg Oral
Subject bersacapavir Other / unclassified 250 mg Oral
Subject bersacapavir Other / unclassified 600 mg Oral