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Clinical Trial Summary

The study will evaluate patients diagnosed with POAG or OHT who are switched to GANFORT® UD (unit dose of fixed combination bimatoprost and timolol) therapy for medical reasons in accordance with physician standard clinical practice. All treatment decisions lie with the physician.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01999348
Study type Observational
Source Allergan
Contact
Status Completed
Phase
Start date November 25, 2013
Completion date December 19, 2014

See also
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