drugset / Trial / NCT00601523

Long-term Safety Study of Open-label Pramipexole Extended Release (ER) in Patients With Early Parkinson´s Disease (PD).

NCT00601523

Phase 3 Completed 511 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 ER, in daily doses from 0.375mg to 4.5mg once daily (q.d), in patients who have previously completed a pramipexole double-blind study in early PD (248.524(NCT00479401) or 248.636(NCT00558025) trial).

Timeline

Start
2008-01
Primary completion
2010-06
Completion

Drugs

EvaluationDrugModalityDoseRoute
Comparator Pramipexole Unknown 0.375 mg
Comparator Pramipexole Unknown 4.5 mg

Indications