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Clinical Trial Summary

The trial will evaluate the safety and efficacy of 3 dose regimens of H-1337 [0.6% twice daily (b.i.d.), 1.0% b.i.d. and 1.0% once in the morning (q.a.m.), and timolol maleate (0.5%, b.i.d.) in both eyes for 28 days.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05913232
Study type Interventional
Source D. Western Therapeutics Institute, Inc.
Contact DWTI CTA
Status Recruiting
Phase Phase 2
Start date August 28, 2023
Completion date December 2025

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