- Trials with a EudraCT protocol (1)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
1 result(s) found for: 2006-006431-42.
Displaying page 1 of 1.
EudraCT Number: 2006-006431-42 | Sponsor Protocol Number: 248.629 | Start Date*: 2007-05-30 | |||||||||||
Sponsor Name:Boehringer Ingelheim Pharma GmbH & Co. KG | |||||||||||||
Full Title: A phase IV randomised, double-blind, placebo-controlled, dose titration trial with pramipexole (Sifrol®, Mirapexin®) 0.125-0.75 mg/day per os to investigate the long-term efficacy, safety and toler... | |||||||||||||
Medical condition: Restless Legs Syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) SK (Completed) FI (Completed) IE (Completed) BE (Completed) AT (Completed) GR (Prematurely Ended) GB (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
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