drugset / Trial / NCT00577460

Long-term Safety Study of Open-label Pramipexole ER in Patients With Advanced PD

NCT00577460

Phase 3 Completed 391 enrolled Boehringer Ingelheim
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The general aim of this study is to obtain long-term safety and tolerability data on pramipexole extended release (ER), in daily doses from 0.375mg to 4.5mg once daily (qd), in patients who have previously completed a pramipexole double-blind study in advanced Parkinson's disease (PD) (248.525 trial).

Timeline

Start
2007-12
Primary completion
2010-06
Completion

Drugs

EvaluationDrugModalityDoseRoute
Comparator Pramipexole Unknown 0.375 mg
Comparator Pramipexole Unknown 4.5 mg

Indications