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

H

Huons

Status and phase

Enrolling
Phase 3

Conditions

Primary Open Angle Glaucoma (POAG)
Ocular Hypertension

Treatments

Drug: HUC3-637
Drug: HUC3-637-R

Study type

Interventional

Funder types

Industry

Identifiers

NCT07335211
HUC3-637

Details and patient eligibility

About

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

Enrollment

206 estimated patients

Sex

All

Ages

19+ years old

Volunteers

No Healthy Volunteers

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)

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

206 participants in 2 patient groups

HUC3-637
Experimental group
Description:
Dorzolamide, Timolol
Treatment:
Drug: HUC3-637
HUC3-637-R
Active Comparator group
Description:
Dorzolamide, Timolol
Treatment:
Drug: HUC3-637-R

Trial contacts and locations

1

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Central trial contact

Rang Lee

Data sourced from clinicaltrials.gov

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