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NCT00721656

A Randomized, Double Blind, Placebo Controlled, Phase 2 Study of KLS-0611 in Patients With Dry Eye Syndromes

Completed Phase 2 Last updated 16 March 2009
What this trial tests

Phase 2 trial testing Placebo in Dry Eye Syndromes in 80 participants. Completed.

Quick facts

Lead sponsorKissei Pharmaceutical Co., Ltd.
PhasePhase 2
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingtriple
Primary purposetreatment
Enrollment80
Sites5 locations across Japan

Drugs / interventions tested

Conditions studied

Sponsor

Kissei Pharmaceutical Co., Ltd. — full company profile →

Who can join

20 and older, any sex, with Dry Eye Syndromes. Patients with the condition only — healthy volunteers not accepted.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

To evaluate the efficacy and safety of KLS-0611 compared to placebo in patients with dry eye syndromes.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Dry Eye Syndromes

Currently open trials in the same condition.

Other Kissei Pharmaceutical Co., Ltd. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT00721656.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing