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NCT00370747

Efficacy and Safety of Ecabet Ophthalmic Solution for the Treatment of Dry Eye Syndrome

Completed Phase 2 Last updated 13 March 2013
What this trial tests

Phase 2 trial testing Ecabet in Dry Eye Syndromes in 162 participants. Completed in 1 June 2007.

Timeline
1 September 2006
Primary endpoint
1 June 2007
1 June 2007

Quick facts

Lead sponsorBausch & Lomb Incorporated
PhasePhase 2
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment162
Start date1 September 2006
Primary completion1 June 2007
Estimated completion1 June 2007
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Bausch & Lomb Incorporated — full company profile →

Who can join

18 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

The purpose of this study is to determine whether ecabet ophthalmic solution is an effective treatment for dry eye syndrome

Publications & conference data

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

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Other recruiting trials for Dry Eye Syndromes

Currently open trials in the same condition.

Other Bausch & Lomb Incorporated 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/NCT00370747.

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