Trial Profile

A Multiple Dose Study With Increasing Pramipexole Doses (0.375 mg to 4.5 mg q.d.) of Oral Extended Release (ER) Tablets With a Three-way Cross Comparison of 4.5 mg Pramipexole ER q.d. Fasted Versus 4.5 mg Pramipexole ER q.d. Fed Versus 1.5 mg Pramipexole Immediate Release Tablets t.i.d. Fasted in Healthy Male Volunteers

Status: Completed

Phase of Trial: Phase I

Latest Information Update: 15 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 Pharmacokinetics
Sponsors Boehringer Ingelheim

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