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A Phase III double-blind, double-dummy, placebo-controlled, 8 week fixed dose trial with pramipexole IR (Mirapex, Mirapexin, Pexola, Sifrol) 0.125 and 0.5 mg/day administered orally to investigate the efficacy and safety in patients 6-17 years of age diagnosed with Tourette Syndrome according to DSM-IV criteria

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Trial Profile

A Phase III double-blind, double-dummy, placebo-controlled, 8 week fixed dose trial with pramipexole IR (Mirapex, Mirapexin, Pexola, Sifrol) 0.125 and 0.5 mg/day administered orally to investigate the efficacy and safety in patients 6-17 years of age diagnosed with Tourette Syndrome according to DSM-IV criteria

Status: Completed
Phase of Trial: Phase III

Latest Information Update: 31 May 2011

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At a glance

  • Drugs Pramipexole (Primary)
  • Indications Gilles de la Tourette's syndrome
  • Focus Therapeutic Use

Most Recent Events

  • 31 May 2011 New trial record

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