An Extension Study of KCT-0809 in Dry Eye Patients With Sjögren's Syndrome

NCT02503176 · Status: TERMINATED · Phase: PHASE3 · Type: INTERVENTIONAL

Last updated 2018-03-05

No results posted yet for this study

Summary

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.

Conditions

  • Dry Eye With Sjögren's Syndrome

Interventions

DRUG

KCT-0809 ophthalmic solution

Sponsors & Collaborators

  • Kissei Pharmaceutical Co., Ltd.

    lead INDUSTRY

Eligibility

Min Age
20 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Primary Completion
2017-05-29

Countries

  • Japan

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02503176 on ClinicalTrials.gov