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Clinical Trial Summary

To investigate whether the IOP lowering efficacy of STN1012600 ophthalmic solution 0.002% is non-inferior to that of latanoprost 0.005% in subjects with POAG or OHT after treatment for 4 weeks.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05495061
Study type Interventional
Source Santen Pharmaceutical Co., Ltd.
Contact
Status Completed
Phase Phase 3
Start date August 9, 2022
Completion date April 18, 2023