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Phase 3 Study of DE-114A Ophthalmic Solution in Patients With Allergic Conjunctivitis

A long-term Study of DE-114A Ophthalmic Solution in Patients with Allergic Conjunctivitis - Phase 3 -

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT2080223566
Enrollment
120
Registered
2017-06-22
Start date
2017-06-18
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Allergic Conjunctivitis

Interventions

Sponsors

SANTEN PHARMACEUTICAL CO., LTD.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Provided signed, written informed consent. Has a positive result from a Type I allergy test.

Exclusion criteria

Exclusion criteria: Eye disease other than allergic conjunctivitis is present and requires treatment. Females who are pregnant, nursing or planning a pregnancy, or females of childbearing potential who are not using a reliable method of contraception.

Design outcomes

Primary

MeasureTime frame
efficacy Subjective symptom

Secondary

MeasureTime frame
efficacy Objective symptom

Countries

Japan

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026