Clinical Trial Results:
Multicenter, Double-Blind, Randomized, Controlled, Parallel Comparison of Efficacy and Safety of Fixed Doses of Two Formulations of Botulinum Toxin Type A in the Treatment of Moderate to Severe Cervical Dystonia (BOTOX® 200 Units and Dysport® 750 Units)
Summary
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EudraCT number |
2006-006449-14 |
Trial protocol |
DE IT |
Global completion date |
25 Sep 2009
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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 MedAff-BTX-0616 - Eudra 2006-006449-14 |
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.