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Last Updated: May 15, 2024

CLINICAL TRIALS PROFILE FOR JNJ-42165279


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Clinical Trials for JNJ-42165279

Trial ID Title Status Sponsor Phase Summary
NCT01650597 ↗ A Single Ascending Dose Study to Investigate the Safety, Tolerability, and Pharmacokinetics of JNJ-42165279 in Healthy Male Participants Completed Janssen-Cilag International NV Phase 1 The purpose of this study is to investigate the safety, tolerability and pharmacokinetics of single ascending doses as well as repeated doses of JNJ-42165279 in healthy male participants.
NCT01826786 ↗ The Effects of JNJ-42165279 on the Neural Basis of Anxiety Disorders in Healthy Male Volunteers Completed Janssen Research & Development, LLC Phase 1 The purpose of this study is to evaluate the potential efficacy of JNJ-42165279 in treating anxiety disorders through evaluation of brain activation patterns using imaging technology in healthy volunteers.
NCT01964651 ↗ Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of JNJ-42165279 in Healthy Young and Elderly Participants Completed Janssen Research & Development, LLC Phase 1 The purpose of this study is to assess the safety, tolerability, and pharmacokinetics of JNJ-42165279 in healthy, young and elderly, male and female participants after repeated oral dose administration.
NCT02065739 ↗ A Study to Investigate the Effects of Itraconazole on the Pharmacokinetics of JNJ-42165279 in Healthy Male Participants Completed Janssen Pharmaceutica N.V., Belgium Phase 1 The purpose of this study is to assess the effects of repeated administration of 200 mg of itraconazole on the single-dose pharmacokinetics of JNJ-42165279 in healthy male participants.
NCT02169973 ↗ A Study to Investigate the Regional Brain Kinetics of the Positron Emission Tomography Ligand 11C-MK-3168 and the Blocking of the Retention of the Ligand in the Human Brain by JNJ-42165279 Completed Janssen Research & Development, LLC Phase 1 The purpose of the study is to measure the uptake, distribution, and clearance of 11C-MK-3168 by Positron Emission Tomography (PET) scan and to model the tissue specific kinetics of 11C-MK-3168 with the appropriate input function in human brain in Part A; to measure blocking of retention of 11C-MK-3168 at the estimated time to maximum plasma concentration after dosing (tmax) following each single oral doses of JNJ-42165279 and model the exposure/enzyme interaction of JNJ-42165279 in Part B; to measure the saturation of enzyme inhibition in the brain at steady state plasma concentrations of JNJ-42165279 (on Day 8) after 7 once-daily doses of JNJ-42165279 by conducting PET studies with 11C-MK-3168 at trough plasma concentrations on Day 2 in Part C.
NCT02432703 ↗ A Safety and Efficacy Study of JNJ-42165279 in Participants With Social Anxiety Disorder Completed Janssen Research & Development, LLC Phase 2 The purpose of this study is to investigate the efficacy of JNJ-42165279 during 12 weeks of treatment in participants with Social Anxiety Disorder (SAD).
>Trial ID >Title >Status >Phase >Summary

Clinical Trial Conditions for JNJ-42165279

Condition Name

Condition Name for
Intervention Trials
Healthy 5
Healthy Volunteers 1
Pharmacokinetics 1
Phobic Disorders 1
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Condition MeSH

Condition MeSH for
Intervention Trials
Disease 3
Anxiety Disorders 2
Depressive Disorder 1
Depression 1
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Clinical Trial Locations for JNJ-42165279

Trials by Country

Trials by Country for
Location Trials
United States 30
Belgium 4
Canada 2
United Kingdom 1
Australia 1
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Trials by US State

Trials by US State for
Location Trials
California 5
Florida 3
New York 3
Utah 2
Texas 2
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Clinical Trial Progress for JNJ-42165279

Clinical Trial Phase

Clinical Trial Phase for
Clinical Trial Phase Trials
Phase 2 3
Phase 1 6
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Clinical Trial Status

Clinical Trial Status for
Clinical Trial Phase Trials
Completed 8
Recruiting 1
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Clinical Trial Sponsors for JNJ-42165279

Sponsor Name

Sponsor Name for
Sponsor Trials
Janssen Research & Development, LLC 7
Janssen Pharmaceutica N.V., Belgium 1
Janssen-Cilag International NV 1
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Sponsor Type

Sponsor Type for
Sponsor Trials
Industry 9
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