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Recruiting Phase 3

Efficacy and Safety of HUC3-637 in Patients With Primary Open Angle Glaucoma or Ocular Hypertension

NCT07335211 · tracked via the Priya Life Science South Korea tracker
Phase
Phase 3
Started
2026-01
Last updated
2026-01-13

Condition(s) studied

Primary Open Angle Glaucoma (POAG)Ocular Hypertension

Investigational drug(s) / intervention(s)

HUC3-637HUC3-637-R

HUC3-637: Ophthalmic solution instilled directly into the eye (topical ocular administration)

HUC3-637-R: Ophthalmic solution instilled directly into the eye (topical ocular administration)

Study summary

A multicenter, randomized, single-blind, active controlled, phase III clinical trial to evaluate the efficacy and safety of HUC3-637 in patients with primary open angle glaucoma or ocular hypertension

Eligibility

Sex
ALL
Min age
19 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Adults aged 19 years and older * Participants diagnosed with POAG or OH * Have fully explained and understood the study and have voluntarily given written informed consent. Exclusion Criteria: * Acute or chronic angle-closure glaucoma * Congenital glaucoma, secondary glaucoma (open-angle glaucoma)

Primary outcome measure(s)

  • Mean change in diurnal IOP — 12 week

Trial sites (1)

FacilityCityRegionStatus
Kangbuk Samsung Hospital Seoul South Korea Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07335211 on ClinicalTrials.gov ↗ ← All trials in South Korea