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RECRUITING
NCT07615426
PHASE1

A Study of the Feasibility, Safety and Tolerability of Aticaprant as Adjunctive Treatment in Participants With Schizophrenia

Sponsor: Janssen Research & Development, LLC

View on ClinicalTrials.gov

Summary

The purpose of this study is to see how feasible it is to enroll participants with schizophrenia and for them to complete the study/assessments. It will also assess how safe and tolerable aticaprant is when compared with placebo in participants with schizophrenia.

Official title: A Randomized, Double-blind, Multicenter, Placebo-controlled, Parallel-group, Phase 1b Study to Investigate the Feasibility, Safety and Tolerability of Aticaprant as Adjunctive Treatment in Participants With Schizophrenia

Key Details

Gender

All

Age Range

18 Years - 55 Years

Study Type

INTERVENTIONAL

Enrollment

64

Start Date

2026-03-02

Completion Date

2027-06-21

Last Updated

2026-06-05

Healthy Volunteers

No

Conditions

Interventions

DRUG

Aticaprant

Participants will receive aticaprant during the double blind (DB) treatment phase.

DRUG

Placebo

Participants will receive placebo during the DB treatment phase.

Locations (8)

CNS Network

Garden Grove, California, United States

Synexus Clinical Research US Inc

Atlanta, Georgia, United States

Uptown Research Institute

Chicago, Illinois, United States

Western Michigan University

Kalamazoo, Michigan, United States

Neurobehavioral Research Inc

Cedarhurst, New York, United States

Evolution Research Group

Staten Island, New York, United States

Community Clinical Research, Inc.

Austin, Texas, United States

Pillar Clinical Research, LLC

Richardson, Texas, United States