Clinical Trial Results:
A Multicenter, Double-masked, Randomized, Parallel Study of the Safety and Efficacy of Bimatoprost 0.03%/Timolol 0.5% Preservative freeOphthalmic Solution Compared with GANFORT® (bimatoprost 0.03%/timolol 0.5% ophthalmic solution) Once Daily for 12 Weeks in Patients with Glaucoma or Ocular Hypertension
Summary
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EudraCT number |
2010-021507-24 |
Trial protocol |
DE HU CZ GB ES |
Global completion date |
20 Feb 2012
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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 |
03 Nov 2016
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First version publication date |
03 Nov 2016
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Other versions |
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Summary report(s) |
CT.gov Summary Results - Study 192024-050 - Eudra 2010-021507-24 |
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.