Trial Profile

A Multiple Dose Study of Pramipexole With Increasing Doses (0.375 mg to 1.5 mg q.d.) of Oral Extended Release (ER) Tablet in Two-way Cross-over Comparison of 0.375 mg ER Tablet q.d. Versus 0.125 mg Immediate Release (IR) Tablet t.i.d. and 1.5 mg ER Tablet q.d. Versus 0.5 mg IR Tablet t.i.d. in Japanese Healthy Male Volunteers

Status: Completed

Phase of Trial: Phase I

Latest Information Update: 22 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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