EligibleTrials

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

Recruiting · NCT07615426 · Interventional (participants receive a specific treatment) · Lead sponsor: Janssen Research & Development, LLC

View the official record on ClinicalTrials.gov →
Schizophrenia

Interventions studied

AticaprantPlacebo

What this trial is about

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.

Who can take part

Age range
18 Years to 55 Years
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Phase 1
Study type
Interventional (participants receive a specific treatment)

Inclusion criteria

Exclusion criteria

Where it is running

8 locations listed across 6 US states.

Read the full protocol, contacts and eligibility on ClinicalTrials.gov →

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