A Phase 3 Prospective, Randomized, Double-Masked, 12-Week, Parallel Group Study In Pediatric Subjects With Glaucoma.

Completed · Phase 3

Conditions studied: Glaucoma

In brief

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.

Key facts

Study ID
NCT00716859
Run by
Pfizer's Upjohn has merged with Mylan to form Viatris Inc.
People needed
139
Starts
2008-07-01
Expected to finish
2009-11-01
Last updated by the study team
2021-02-03

Who can join

Age: 1 and older, up to 18. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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