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Last Updated: December 11, 2024

CLINICAL TRIALS PROFILE FOR JNJ-56136379


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Clinical Trials for JNJ-56136379

Trial ID Title Status Sponsor Phase Summary
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 Chro Completed Janssen Sciences Ireland UC Phase 1 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).
NCT02933580 ↗ A Study to Investigate Safety, Tolerability, and Pharmacokinetics of JNJ-56136379 in Healthy Japanese Adult Participants Completed Janssen Research & Development, LLC Phase 1 The purpose of this study is to investigate the safety, tolerability, and pharmacokinetics (PK) of JNJ-56136379 in healthy Japanese adult participants following oral administration of single doses from 25 milligram (mg) up to 600 mg, in fasted conditions.
NCT03111511 ↗ A Study in Healthy Female Participants to Investigate the Effect of JNJ-56136379 at Steady-state on the Single-dose Pharmacokinetics of Ethinylestradiol and Drospirenone (Oral Contraceptive) and on the Single-dose Pharmacokinetics of Midazolam (Prob Completed Janssen Sciences Ireland UC Phase 1 The main purpose of this study is to evaluate the effect of steady-state concentrations of JNJ-56136379 on the single-dose pharmacokinetics (PK) of drospirenone and ethinylestradiol (oral contraceptive [OC]) in healthy female participants and to evaluate the effect of steady-state concentrations of JNJ-56136379 on the single-dose PK of midazolam (sensitive probe substrate for CYP3A4) in healthy female participants.
NCT03361956 ↗ An Efficacy, Safety, and Pharmacokinetics Study of JNJ-56136379 in Participants With Chronic Hepatitis B Virus Infection Completed Janssen Sciences Ireland UC Phase 2 The main purpose of this study is to evaluate efficacy of 24 weeks of study treatment, in terms of changes in hepatitis B surface antigen (HBsAg) levels.
>Trial ID >Title >Status >Phase >Summary

Clinical Trial Conditions for JNJ-56136379

Condition Name

Condition Name
Intervention Trials
Healthy 6
Hepatitis B, Chronic 5
Hepatitis B 2
Hepatitis, Chronic 1
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Condition MeSH

Condition MeSH
Intervention Trials
Hepatitis 8
Hepatitis B, Chronic 8
Hepatitis B 8
Hepatitis A 8
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Clinical Trial Locations for JNJ-56136379

Trials by Country

Trials by Country
Location Trials
United States 23
Canada 11
Belgium 8
Germany 8
France 7
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Trials by US State

Trials by US State
Location Trials
California 4
Florida 2
Maryland 2
Pennsylvania 2
New York 2
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Clinical Trial Progress for JNJ-56136379

Clinical Trial Phase

Clinical Trial Phase
Clinical Trial Phase Trials
Phase 2 7
Phase 1 8
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Clinical Trial Status

Clinical Trial Status
Clinical Trial Phase Trials
Completed 7
Active, not recruiting 3
Recruiting 3
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Clinical Trial Sponsors for JNJ-56136379

Sponsor Name

Sponsor Name
Sponsor Trials
Janssen Sciences Ireland UC 8
Janssen Research & Development, LLC 8
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Sponsor Type

Sponsor Type
Sponsor Trials
Industry 16
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