A Phase 3 Prospective, Randomized, Double-Masked, 12-Week, Parallel Group Study In Pediatric Subjects With Glaucoma. - NCT00716859-89052 (Clinical Trial 231239)
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Henderson |
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NV |
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89052 |
| Conditions: |
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Glaucoma |
| Purpose: |
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To assess the effectiveness of latanoprost 0.005% ophthalmic solution dosed once-daily and
timolol 0.5% dosed twice-daily in paediatric subjects of 18 years of age or under who are
diagnosed with glaucoma.
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| Study summary: |
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This study is no longer available. |
| Criteria: |
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This study is no longer available. |
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If you are interested in this clinical trial please use the contact information above. If you would like to get additional information about this clinical trial please visit ClinicalTrials.gov.
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| Data Source: |
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ClinicalTrials.gov |
| Date Processed: |
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December 30, 2009 |
Modifications to
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Only selected fields are shown, please use the link
above to view all information about this clinical trial. |
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Clinical trials are medical research studies designed to test the safety and/or
effectiveness of new drugs, devices, or treatments in humans. These studies are
conducted worldwide for a range of conditions and illnesses. Learn more about
clinical research and participating in a study at
About Clinical Trials.
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