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A Randomised, Double Blind Study Comparing Fixed Doses of 0.25mg, 0.5mg and 0.75mg Pramipexole to Investigate the Efficacy and Safety in Patients With Idiopathic Restless Legs Syndrome for 6 Weeks, Followed by 46 Weeks Open Label Long Term Study to Investigate the Safety and Efficacy of Pramipexole

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Trial Profile

A Randomised, Double Blind Study Comparing Fixed Doses of 0.25mg, 0.5mg and 0.75mg Pramipexole to Investigate the Efficacy and Safety in Patients With Idiopathic Restless Legs Syndrome for 6 Weeks, Followed by 46 Weeks Open Label Long Term Study to Investigate the Safety and Efficacy of Pramipexole

Status: Completed
Phase of Trial: Phase III

Latest Information Update: 25 Jun 2014

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At a glance

  • Drugs Pramipexole (Primary)
  • Indications Restless legs syndrome
  • Focus Therapeutic Use
  • Sponsors Boehringer Ingelheim
  • Most Recent Events

    • 08 Aug 2009 Status changed from active, no longer recruiting to completed.
    • 11 Jun 2009 Results preseneted at the 13th International Congress of Parkinson's Disease and Movement Disorders
    • 11 Jun 2009 Status change from active, no longer recruiting to completed
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