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A study assessing IOP fluctuations of K-115 in combination with latanoprost

Phase 3
Conditions
POAG or OH
Registration Number
JPRN-jRCT2080222237
Lead Sponsor
Kowa Co., Ltd.
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Sex
All
Target Recruitment
26
Inclusion Criteria

1. Patients with POAG or OH
2. IOP after a run-in period with latanoprost>=18mmHg

Exclusion Criteria

1.Patients with decreased visual performance
2.Patients thought to use glaucoma medication during this trial
3.Patients thought to wear contact lenses during this trial
etc.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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