Efficacy of NBI-1117568 in Preventing Relapse in Adults With Schizophrenia
Neurocrine Biosciences · NCT07227818
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18–65 · All sexes
- Healthy volunteers
- Not accepted (a condition is required)
- Study type
- Interventional · Phase 3
- Target enrollment
- 560
- US sites recruiting
- 20
- Study start
- December 16, 2025
- Record last updated
- September 25, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
The main objective of the study is to evaluate NBI-1117568 compared with placebo in delaying relapse of symptoms of schizophrenia in adults who have a stable response after open-label treatment with NBI-1117568.
Being studied: NBI-1117568; Placebo
Conditions: Schizophrenia
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Key Inclusion Criteria
- Participant has a primary diagnosis of schizophrenia established by a comprehensive psychiatric evaluation based on the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition, Text Revision (DSM-5-TR) criteria.
- Participant had the initial diagnosis of schizophrenia ≥1 year before screening.
- Participant has had a positive response to ≥1 antipsychotic therapy (other than clozapine) at a therapeutic dose.
Key Exclusion Criteria
- Participant has an unstable or poorly controlled medical condition or chronic disease (including history of neurological [including dementing illness, myasthenia gravis], hepatic, renal, cardiovascular, gastrointestinal, pulmonary, autoimmune, or endocrine disease that may affect study participation or results) or malignancy within 30 days before Day 1.
- Participant has any laboratory abnormalities suggestive of clinically significant, poorly managed, or unmanaged undiagnosed disease.
- Participant has a history of clozapine treatment for treatment-resistant psychosis.
- Participant has a history of a stay in a psychiatric inpatient facility for ≥30 consecutive days (other than for purely social reasons or due to participation in a different clinical trial) during the 90 days before screening.
- Participant has initiated or increased intensity of nonpharmacological psychosocial therapeutic treatment within 3 weeks before screening or is expected to change throughout the length of the study.
Note: Other protocol-defined Inclusion and Exclusion criteria may apply.
Recruiting US locations
Neurocrine Clinical Site
Garden Grove, CA 92845
Neurocrine Clinical Site
La Habra, CA 90631
Neurocrine Clinical Site
Lemon Grove, CA 91945
Neurocrine Clinical Site
Oceanside, CA 92056
Neurocrine Clinical Site
Torrance, CA 90504
Neurocrine Clinical Site
Hollywood, FL 33024
Neurocrine Clinical Site
Maitland, FL 32751
Neurocrine Clinical Site
Miami, FL 33122
Neurocrine Clinical Site
Miami, FL 33155
Neurocrine Clinical Site
Tampa, FL 33629
Neurocrine Clinical Site
West Palm Beach, FL 33024
Neurocrine Clinical Site
Atlanta, GA 30318
Neurocrine Clinical Site
Boston, MA 02116
Neurocrine Clinical Site
Flowood, MS 39232
Neurocrine Clinical Site
Marlton, NJ 08054
Neurocrine Clinical Site
Cedarhurst, NY 11516
Neurocrine Clinical Site
New York, NY 10029
Neurocrine Clinical Site
The Bronx, NY 10461
Neurocrine Clinical Site
DeSoto, TX 75115
Neurocrine Clinical Site
Bellevue, WA 98007
Study contacts (from the official record)
- Neurocrine Medical Information Call Center · 1-877-641-3461 · medinfo@neurocrine.com
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