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NCT03830359

Efficacy, Safety of T2769 in Dry Eye Disease

Completed NA Results posted Last updated 16 March 2022
What this trial tests

NA trial testing T2769 in Dry Eye Syndrome in 62 participants. Completed in 18 February 2019.

Timeline
1 September 2018
Primary endpoint
18 February 2019
18 February 2019

Quick facts

Lead sponsorLaboratoires Thea
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposeother
Enrollment62
Start date1 September 2018
Primary completion18 February 2019
Estimated completion18 February 2019
Sites3 locations across Tunisia

Drugs / interventions tested

Conditions studied

Sponsor

Laboratoires Thea — full company profile →

Who can join

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

Results — posted to ClinicalTrials.gov

Per-arm endpoint measurements with 95% confidence intervals where reported. Source: trial results section.

Ocular Symptomatology Primary · Baseline and Day 42

Change from baseline in ocular symptomatology on a Visual Analog Scale (0=No discomfort and 100=Maximal discomfort) at Day 42.

GroupValue95% CI
T2769-55.9± 23.1

Sponsor's own description

Efficacy of T2769 in Dry Eye Desease

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 trials of T2769

Trials testing the same drug.

Other recruiting trials for Dry Eye Syndrome

Currently open trials in the same condition.

Other Laboratoires Thea 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/NCT03830359.

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