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 | |
|     EudraCT number | 2010-021507-24 | 
|     Trial protocol | DE HU CZ GB ES | 
|     Global completion date | 
                                    20 Feb 2012
                             | 
|     Paediatric regulatory details | |
|     Is the trial part of an agreed EMA paediatric investigation plan? | 
                                        No
                                 | 
|     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
                                 | 
|     Results information | |
|     Results version number | v1(current) | 
|     This version publication date | 
                                    03 Nov 2016
                             | 
|     First version publication date | 
                                    03 Nov 2016
                             | 
|     Other versions | |
|     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.    
 
				
