Clinical Trial Results:
            A double-blind, double-dummy, placebo-controlled, randomized, three parallel groups study comparing the Efficacy, Safety and Tolerability of Pramipexole ER versus placebo and versus Pramipexole IR administered orally over a 26-week maintenance phase in L-Dopa+ treated patients with advanced Parkinson’s disease (PD).
    
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                 Summary 
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    EudraCT number  | 
        2007-000074-23 | 
    Trial protocol  | 
        GB SE IT CZ HU AT SK ES | 
    Global completion date  | 
        
                                    19 Nov 2008
                             
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                 Paediatric regulatory details 
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    Is the trial part of an agreed EMA paediatric investigation plan?  | 
        
                                        No
                                 
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    Is the trial in scope of article 45 of Regulation (EC) No 1901/2006?  | 
        
                                        No
                                 
         | 
    
    Is the trial in scope of article 46 of Regulation (EC) No 1901/2006?  | 
        
                                        No
                                 
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                 Results information 
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    Results version number  | 
        v1(current) | 
    This version publication date  | 
        
                                    16 May 2016
                             
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    First version publication date  | 
        
                                    06 May 2015
                             
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    Other versions  | 
        |
    Summary report(s)  | 
                                248.525 | 
    
            Note: The legislation allows summary attachments to be posted instead of the full dataset for this trial. Refer to            Commission Guideline 2012/C 302/03
            for further information.