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A Multicenter, Open-label, Sequential Cohort, Dose-escalation, 14-day Study to Explore the Tolerability and Pharmacokinetics of Iloperidone 12 to 24 mg/Day Followed by 26 Weeks of Flexible Dosing (6 to 24 mg/Day) in Adolescent Patients (Aged 12 to 17 Years).

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A Multicenter, Open-label, Sequential Cohort, Dose-escalation, 14-day Study to Explore the Tolerability and Pharmacokinetics of Iloperidone 12 to 24 mg/Day Followed by 26 Weeks of Flexible Dosing (6 to 24 mg/Day) in Adolescent Patients (Aged 12 to 17 Years).

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 15 Jun 2016

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At a glance

  • Drugs Iloperidone (Primary)
  • Indications Schizophrenia
  • Focus Adverse reactions; Pharmacokinetics
  • Sponsors Novartis; Vanda Pharmaceuticals

    • Most Recent Events

    • 10 Jun 2016 Status changed from active, no longer recruiting to completed.
    • 08 Apr 2015 Planned End Date changed from 1 Feb 2015 to 1 Aug 2015 as reported by ClinicalTrials.gov record.
    • 08 Apr 2015 Planned primary completion date changed from 1 Feb 2015 to 1 Aug 2015 as reported by ClinicalTrials.gov record.

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