Clinical trial

Observational Study to Evaluate Risks of Side Effects, Drug Abuse and Dependence…

NCT00244465 · UCB Pharma, Industry · Completed

Key facts

NCT number NCT00244465
Title Observational Study to Evaluate Risks of Side Effects, Drug Abuse and Dependence in Patients Who Received Xyrem ® on Prescription
Official title 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.
Lead sponsor UCB Pharma, Industry
Status Completed
Study type Observational
Conditions Narcolepsy
Enrollment 750
Start date May 1, 2006
Primary completion Sep 1, 2016
Completion Sep 1, 2016
First posted Oct 26, 2005
Last update posted Sep 7, 2016
Countries Austria, Belgium, Czechia, Germany, Ireland, Italy, Spain, Switzerland, United Kingdom

At a glance

  • 10–99 Study sites
  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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