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NBI-1117568-SCZ3030: Evaluation of NBI-1117568 in Inpatient Adults With Schizophrenia

NCT07105098

This study is recruiting at 6 US sites in 4 states, according to its ClinicalTrials.gov record last updated .

Summary

The primary objective for this study is to evaluate the efficacy of NBI-1117568 compared with placebo on improving behavioral and psychological symptoms of schizophrenia in adults.

Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov

Conditions studied

  • Schizophrenia

Eligibility basics and study details

Study type
Interventional
Phase
Phase 3
Ages
18 to 65 years
Sex
All
Healthy volunteers
Not accepted
Sponsor
Neurocrine Biosciences
Last updated on ClinicalTrials.gov
September 25, 2026

These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.

US recruiting sites

Arkansas · 1

  • Neurocrine Clinical Site · Little Rock, AR

California · 3

  • Neurocrine Clinical Site · Culver City, CA
  • Neurocrine Clinical Site · Garden Grove, CA
  • Neurocrine Clinical Site · Riverside, CA

Florida · 1

  • Neurocrine Clinical Site · Hollywood, FL

Ohio · 1

  • Neurocrine Clinical Site · North Canton, OH

Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.