Skip to content
Study details
Enrolling now

A Study to Assess Adverse Events, Change in Disease Activity, and How Oral Emraclidine Moves Through the Body in Adult Participants With Schizophrenia

AbbVie
NCT IDNCT07145918ClinicalTrials.gov data as of Apr 2026
Phase

Phase 2

Target enrollment

258

Study length

about 2.6 years

Ages

18–65

Locations

7 sites in AR, CA, MD +2

About this study

Researchers are testing a treatment called emraclidine for people with schizophrenia. The trial will look at any side effects that may occur, how well the treatment works to reduce symptoms of schizophrenia, and how the drug moves through your body. Participants will receive either oral emraclidine or placebo for up to 42 days.

Based on ClinicalTrials.gov records.

What participants do

  • 1.Take Emraclidine
  • 2.Take Placebo
PhasePhase 2
Primary goalNumber of Participants with Adverse Events (AEs)

Participation effort

Estimated from trial records. Details can vary by site.

Time + visits
Low6%
Logistics
Moderate50%

Logistics difficulty varies by site location and availability.

Trial highlights

Treatment details

Auto-extracted from trial records to preview treatments and outcomes.

Endpoints

Primary: Number of Participants with Adverse Events (AEs), Part A Only- Accumulation ratio for Cmax (RacCmax) of Emraclidine, Part A Only- Terminal Phase Elimination Half-Life (t1/2) of Emraclidine, Part A Only-Apparent Clearance of Drug from Plasma (CL/F) of Emraclidine, Part A Only-Maximum Observed Plasma Concentration (Cmax) of Emraclidine, Part A Only-Maximum Observed Plasma Concentration (Cmax) of Metabolite (CV-0000364), Part A Only-Time to Cmax (Tmax) of Emraclidine, Part A Only-Time to Cmax (Tmax) of Metabolite (CV-0000364)

Secondary: Part B Only-Change from Baseline in Positive and Negative Syndrome Scale (PANSS) total score, Part B Only-Change from Baseline in in Clinical Global Impression of Severity (CGIS) score

Body systems

Psychiatry / Mental Health