CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 78 enrolled
Drug / intervention
JNJ-42165279 +1 moredrug
Likely dose
JNJ-42165279 25 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03664232
NCT03664232Phase 2Completed

A Randomized, Double-Blind, Placebo-Controlled, Parallel Group, Multicenter Study Investigating the Efficacy, Safety, and Tolerability of JNJ-42165279 in Adolescent and Adult Subjects With Autism Spectrum Disorder

Janssen Research & Development, LLC·interventional·Posted Sep 10, 2018·Updated Apr 23, 2025

In Brief

A Phase 2 clinical trial evaluating JNJ-42165279 and Placebo for Autism Spectrum Disorder. Completed, enrolled 78 participants across 9 sites.

Detailed Summary

The purpose of this study is to evaluate the efficacy of JNJ-42165279 compared with placebo in the improvement of symptoms of Autism Spectrum Disorder (ASD) during 12 weeks of treatment using the Autism Behavior Inventory (ABI).

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 2CompletedFinished
20192020202120222023202420252026
First PostedSep 10, 2018
Enrollment StartNov 7, 2018
Primary CompletionOct 17, 2022
Study CompletionOct 28, 2022
TodayJul 2, 2026
Enrollment to primary: 3.9 yearsPosted 7.8 years ago

Interventions

JNJ-42165279drug

Participants will receive 25 mg JNJ-42165279 orally twice daily for 12 weeks.

Placebodrug

Participants will receive a matching placebo orally twice daily for 12 weeks.