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RecruitingNCT07114874

Long-term safety of NBI-1117568 in schizophrenia

About this titleRead the official source — NCT07114874

Researchers are studying NBI-1117568, tracking side effects to assess long-term safety and tolerability in adults with schizophrenia.

Medication studyAges 18–65Multiple countries
The study in practice

Understand this study

What is this study about?

Researchers are studying NBI-1117568, tracking side effects to assess long-term safety and tolerability in adults with schizophrenia.

Who could participate?

This study is for people with schizophrenia. Listed age limits: 18 years to 65 years. Other eligibility criteria apply.

What will I do during this study?

Participants receive open-label oral NBI-1117568 once daily for up to 36 months. This is a long-term safety follow-up study.

Listed locations
Bryant and 60 more locationsSee all locations and recruitment
Study phase
Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.

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What to know before participating

A point to clarify

This summary does not cover all risks or eligibility requirements. What risks or changes to my care would apply to me?

Study clarity

Things to check before joining

Study start dateStarted: July 11, 2025
Recruitment status
Recruiting
Enrollment listed in the registry
600
Sponsor
Neurocrine Biosciences
Sponsor type
Biotech company
Study type
Drug
Intervention type
Drug
Study phase
Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.
Locations
United States, Bulgaria, Romania, ...
Age range
From 18 Years to 65 Years
Official registry ID
NCT07114874
Official title
Show the full official title

A Global, Phase 3, Multicenter, Open-Label Study to Assess the Long-Term Safety and Tolerability of NBI-1117568 in Adults With Schizophrenia

Recruitment & locations

Currently recruiting

Bryant, United States · Little Rock, United States · Cerritos, United States

53 more locations
  • Chino, United States
  • Culver City, United States
  • Garden Grove, United States
  • La Habra, United States
  • Lemon Grove, United States
  • Oceanside, United States
  • Pico Rivera, United States
  • Riverside, United States
  • San Diego, United States
  • Sherman, United States
  • Torrance, United States
  • West Hills, United States
  • Atlantis, United States
  • Aventura, United States
  • Doral, United States
  • Hollywood, United States
  • Maitland, United States
  • Miami, United States
  • Miami Lakes, United States
  • Tampa, United States
  • West Palm Beach, United States
  • Atlanta, United States
  • Decatur, United States
  • Peachtree Corners, United States
  • Chicago, United States
  • Oak Brook, United States
  • Gaithersburg, United States
  • Boston, United States
  • Watertown, United States
  • Flowood, United States
  • St Louis, United States
  • Marlton, United States
  • Cedarhurst, United States
  • New York, United States
  • Staten Island, United States
  • The Bronx, United States
  • North Canton, United States
  • Philadelphia, United States
  • Austin, United States
  • DeSoto, United States
  • Houston, United States
  • Orem, United States
  • Bellevue, United States
  • Pleven, Bulgaria
  • Veliko Tarnovo, Bulgaria
  • Vratsa, Bulgaria
  • San Juan, Puerto Rico
  • Brasov, Romania
  • Bucharest, Romania
  • Sânpetru, Romania
  • Belgrade, Serbia
  • Gornja Toponica, Serbia
  • Kragujevac, Serbia

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FAQ

Questions about this study

What is this study about?

Researchers are studying NBI-1117568, tracking side effects to assess long-term safety and tolerability in adults with schizophrenia.

Who is behind this study?

The study sponsor is Neurocrine Biosciences, a biotech company.

Does this study involve medication?

Yes. The study involves medication, including NBI-1117568.

Who can participate?

This study is for people with schizophrenia. Listed age limits: 18 years to 65 years. Other eligibility criteria apply.

Is this study still recruiting?

The registry lists this study as recruiting.

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