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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

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Trial Profile

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

Status: Recruiting
Phase of Trial: Phase IV

Latest Information Update: 06 Mar 2025

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At a glance

  • Drugs Iloperidone (Primary)
  • Indications Bipolar I disorders; Schizophrenia
  • Focus Adverse reactions
  • Sponsors Vanda Pharmaceuticals

    • Most Recent Events

    • 04 Mar 2025 Planned End Date changed from 1 Sep 2024 to 30 Nov 2026.
    • 04 Mar 2025 Planned primary completion date changed from 1 Sep 2024 to 31 Mar 2026.
    • 14 Dec 2022 New trial record

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