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A Long-term Study of KCT-0809 in Dry Eye Patients With Sjögren's Syndrome

NCT ID: NCT02503163

Last Updated: 2017-11-17

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE3

Study Classification

INTERVENTIONAL

Brief Summary

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The purpose of this study is to evaluate of the long-term safety and efficacy of KCT-0809 in dry eye patients with Sjögren's syndrome.

Detailed Description

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Conditions

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Dry Eye With Sjögren's Syndrome

Keywords

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Dry eye syndromes Corneal diseases Conjunctival diseases

Study Groups

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KCT-0809

Group Type EXPERIMENTAL

KCT-0809 ophthalmic solution

Intervention Type DRUG

Interventions

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KCT-0809 ophthalmic solution

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Dry eye patients with Sjögren's syndrome
* Corneal and conjunctival damage

Exclusion Criteria

* Severe ophthalmic disorder
* Punctal plugs or surgery for occlusion of the lacrimal puncta
Minimum Eligible Age

20 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Kissei Pharmaceutical Co., Ltd.

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Multiple Locations, , Japan

Site Status

Countries

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Japan

Other Identifiers

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KCT1303

Identifier Type: -

Identifier Source: org_study_id