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Safety and Efficacy of Combigan® Ophthalmic Solution in Korea

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Allergan

Status

Completed

Conditions

Ocular Hypertension
Glaucoma, Open-Angle

Treatments

Drug: brimonidine tartrate/timolol maleate Ophthalmic Solution

Study type

Observational

Funder types

Industry

Identifiers

NCT01987752
190342-040

Details and patient eligibility

About

This study is a Post-Marketing Surveillance study in Korea to evaluate the safety and efficacy of Combigan® (brimonidine tartrate/timolol maleate) Ophthalmic Solution in patients with Open Angle Glaucoma or Ocular hypertension with insufficient response to local beta blockers treated as per standard of care in clinical practice.

Enrollment

732 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with Open Angle Glaucoma or Ocular Hypertension treated with Combigan® Ophthalmic Solution as standard of care in clinical practice.

Exclusion criteria

  • None.

Trial design

732 participants in 1 patient group

Combigan® Ophthalmic Solution
Description:
Patients treated with Combigan® Ophthalmic Solution as per local standard of care in clinical practice.
Treatment:
Drug: brimonidine tartrate/timolol maleate Ophthalmic Solution

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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