Clinical Trial Results:
            An Open-Label, 2-Period, Crossover Phase 2 Study Comparing the Pharmacokinetics and Tolerability of Dihydroergotamine Mesylate (DHE) Delivered Intravenously (DHE 45) and by Oral Inhalation (MAP0004) in Smoking and Non-Smoking Adult Volunteers 
    
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                 Summary 
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    EudraCT number  | 
        2009-016732-12 | 
    Trial protocol  | 
        GB | 
    Global completion date  | 
        
                                    16 Apr 2010
                             
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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
                                 
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    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  | 
        
                                    05 Nov 2016
                             
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    First version publication date  | 
        
                                    05 Nov 2016
                             
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    Other versions  | 
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    Summary report(s)  | 
                                CT.gov Summary Results - Study MAP0004-CL-P203 - Eudra 2009-016732-12 | 
    
            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.