Safety and Tolerability of Open-Labeled Iloperidone in Adolescents
Recruiting now Phase 4 NCT05648591
Run by Vanda Pharmaceuticals · for 12 to 17 · All sexes
What this study is about
To evaluate the safety and tolerability of iloperidone in adolescent patients with schizophrenia or bipolar I disorder for up to 52 weeks of treatment.
Who can join (things the study team will check)
✅ You may be able to join if…
- Patient is willing and able to provide assent and willing to complete all aspects of the study
- Patient's parent or legal guardian willing and able to provide consent
- Male or female patients 12 through 17 years of age (inclusive)
- Clinical diagnosis of either schizophrenia or bipolar I disorder
🚫 You may not be able to join if…
- Use of other investigational drugs at the time of enrollment, or within 30 days or 5 half-lives of enrollment, whichever is longer
- A positive test for drugs of abuse
Where this trial is running
- Vanda Investigational Site, Little Rock, Arkansas, United States
- Vanda Investigational Site, Denver, Colorado, United States
- Vanda Investigational Site, Atlanta, Georgia, United States
- Vanda Investigational Site, Atlanta, Georgia, United States
- Vanda Investigational Site, Decatur, Georgia, United States
- Vanda Investigational Site, Cincinnati, Ohio, United States
- Vanda Investigational Site, Garfield Heights, Ohio, United States
- Vanda Investigational Site, Westlake, Ohio, United States
- Vanda Investigational Site, Everett, Washington, United States
Who to contact
Vanda Pharmaceuticals Inc. · 202-734-3400 · clinicaltrials@vandapharma.com
It's completely normal to call and ask questions before deciding anything. Mention the study ID: NCT05648591.
Verify everything on the official ClinicalTrials.gov record. Page updated July 2026.
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