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Post Marketing Non-interventional Surveillance Pharmacoepidemiology Study (PMSS) to Evaluate Long-term Safety, Tolerability and Compliance in Administration of Xyrem (Sodium Oxybate) Oral Solution in Patients Who Receive Treatment With This Medication in Regular Clinical Practice.

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Post Marketing Non-interventional Surveillance Pharmacoepidemiology Study (PMSS) to Evaluate Long-term Safety, Tolerability and Compliance in Administration of Xyrem (Sodium Oxybate) Oral Solution in Patients Who Receive Treatment With This Medication in Regular Clinical Practice.

Status: Completed
Phase of Trial: Phase IV

Latest Information Update: 09 Oct 2019

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At a glance

  • Drugs Sodium oxybate (Primary)
  • Indications Hypersomnia; Narcolepsy
  • Focus Adverse reactions; Therapeutic Use
  • Sponsors UCB

    • Most Recent Events

    • 05 Sep 2016 Status changed from active, no longer recruiting to completed.
    • 30 Apr 2015 Status changed from recruiting to active, no longer recruiting as per ClinicalTrials.gov record.
    • 21 Aug 2014 Planned number of patients changed from 1000 to 750 as reported by ClinicalTrials.gov record.

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