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Safety and Efficacy of Relestat Ophthalmic Solution 0.05% for Allergic Conjunctivitis in Korea

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Allergan

Status

Completed

Conditions

Conjunctivitis, Allergic

Treatments

Drug: Relestat Ophthalmic Solution 0.05%

Study type

Observational

Funder types

Industry

Identifiers

NCT01987765
198027-A

Details and patient eligibility

About

This study is a Post-Marketing Surveillance study in Korea to evaluate the safety and efficacy of Relestat Ophthalmic Solution 0.05% in patients with allergic conjunctivitis who are treated with Relestat as standard of care in clinical practice.

Enrollment

847 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with Allergic Conjunctivitis treated with Relestat Ophthalmic Solution in clinical practice.

Exclusion criteria

  • None.

Trial design

847 participants in 1 patient group

Relestat Ophthalmic Solution 0.05%
Description:
Patients who are prescribed Relestat Ophthalmic Solution 0.05% as local standard of care in clinical practice.
Treatment:
Drug: Relestat Ophthalmic Solution 0.05%

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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