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A Study of the Feasibility, Safety and Tolerability of Aticaprant as Adjunctive Treatment in Participants With Schizophrenia
Sponsor: Janssen Research & Development, LLC
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
Aticaprant
Participants will receive aticaprant during the double blind (DB) treatment phase.
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