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A Double-Blind, Randomized, Placebo-Controlled, Multiple-Dose, Multi-Center Safety and Efficacy Study of Co-Administration of Tesofensine/Metoprolol for 12 Weeks in Adult and Adolescent Patients With Prader-Willi Syndrome (PWS), Followed by Two Open Label 12 Weeks Extension Periods for Adolescent Patients

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Trial Profile

A Double-Blind, Randomized, Placebo-Controlled, Multiple-Dose, Multi-Center Safety and Efficacy Study of Co-Administration of Tesofensine/Metoprolol for 12 Weeks in Adult and Adolescent Patients With Prader-Willi Syndrome (PWS), Followed by Two Open Label 12 Weeks Extension Periods for Adolescent Patients

Status: Completed
Phase of Trial: Phase II

Latest Information Update: 29 Feb 2024

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At a glance

  • Drugs Metoprolol/tesofensine (Primary)
  • Indications Prader-Willi syndrome
  • Focus Therapeutic Use
  • Sponsors Saniona

    • Most Recent Events

    • 07 Feb 2020 Status changed from recruiting to completed.
    • 17 Jan 2020 This trial is Completed (Global End Date: 22 Jul 2019), according to European Clinical Trials Database record.
    • 13 May 2019 According to a Saniona media release, ongoing open label study has extended in both Czech Republic and Hungary, and last extension of the study will be completed in July 2019.
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