Trial Profile

A Double-blind, Randomised, Placebo Controlled Study With Two Sequential Two-way Cross-over Parts to Demonstrate That the Influence of Pramipexole up to 4.5 mg Daily on the QT Interval of the ECG in Healthy Male and Female Volunteers is Comparable With Placebo, With a Positive Control (Two-way Cross-over Moxifloxacin Versus Placebo)

Status: Completed

Phase of Trial: Phase I

Latest Information Update: 17 Oct 2014

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At a glance

Drugs Pramipexole (Primary)
Indications Gilles de la Tourette's syndrome; Myoclonus; Parkinson's disease; Restless legs syndrome
Focus Adverse reactions
Sponsors Boehringer Ingelheim

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