🏛️ Verified NIH Record • Updated 2026-05-13

NBI-1117568-SCZ3030: Evaluation of NBI-1117568 in Inpatient Adults With Schizophrenia (NCT07105098)

A Global, Phase 3, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Assess the Efficacy, Safety, and Tolerability of NBI-1117568 in Adults With Schizophrenia Who Warrant Inpatient Hospitalization

🟢 Recruiting Phase3 💊 Investigational Drug / Biologic Sponsor: Neurocrine Biosciences

🩺 Plain-English Summary (8th-Grade Level)

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.

Who can join: Review the eligibility criteria below.

Location: Neurocrine Clinical Site — Culver City, California

Age range: 18 Years to 65 Years

🧪 Interventions in This Study

📋 "Do I Qualify?" — 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria ↗

📍 All Participating Trial Locations (15 Sites)

  • Neurocrine Clinical Site — Culver City, California
  • Neurocrine Clinical Site — Garden Grove, California
  • Neurocrine Clinical Site — Riverside, California
  • Neurocrine Clinical Site — Atlanta, Georgia
  • Neurocrine Clinical Site — North Canton, Ohio
  • Neurocrine Clinical Site — Sliven,
  • Neurocrine Clinical Site — Veliko Tarnovo,
  • Neurocrine Clinical Site — Vratsa,
  • Neurocrine Clinical Site — Győr,
  • Neurocrine Clinical Site — Brasov,
  • Neurocrine Clinical Site — Brasov,
  • Neurocrine Clinical Site — Bucharest,
  • Neurocrine Clinical Site — Belgrade,
  • Neurocrine Clinical Site — Gornja Toponica,
  • Neurocrine Clinical Site — Kragujevac,

📞 Contact the Study Coordinator

Phone: (877) 641-3461

Email: medinfo@neurocrine.com

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

💰 Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

Explore by condition: All Schizophrenia clinical trials

💡 How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
🏛️ View Official NIH Record ↗