Safety and Tolerability of Open-Labeled Iloperidone in Adolescents
Open-label Safety Study of a 1-year 8 to 24 mg/Day Dose Regimen of Iloperidone (FANAPT®) in Adolescent Patients With Schizophrenia or Bipolar I Disorder
Sponsor: Vanda Pharmaceuticals
Listed as NCT05648591, this PHASE4 trial focuses on Bipolar I Disorder and Schizophrenia and remains actively recruiting participants. Sponsored by Vanda Pharmaceuticals, it has been updated 6 times since 2023, reflecting limited change activity. Mental health research at this phase helps define safety and dosing parameters for future study.
Status Flow
Change History
6 versions recorded-
Apr 2025 — Present [monthly]
Recruiting PHASE4
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Sep 2024 — Apr 2025 [monthly]
Recruiting PHASE4
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Jul 2024 — Sep 2024 [monthly]
Recruiting PHASE4
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Apr 2024 — Jul 2024 [monthly]
Recruiting PHASE4
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Jul 2023 — Apr 2024 [monthly]
Recruiting PHASE4
▶ Show 1 earlier version
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Jan 2023 — Jul 2023 [monthly]
Recruiting PHASE4
First recorded
Eligibility Summary
No eligibility information available.
Contact Information
- Vanda Pharmaceuticals
For direct contact, visit the study record on ClinicalTrials.gov .