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Clinical Trial Summary

The purpose of the study is to examine how preservative free tafluprost ophthalmic solution (0.0015%) is distributed in blood circulation after ocular administration in children who have glaucoma or elevated intraocular pressure. Tolerance to the drug and safety in general will also be assessed.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02102750
Study type Interventional
Source Santen Oy
Contact
Status Completed
Phase Phase 1
Start date June 2014
Completion date July 3, 2017

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