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Not Yet RecruitingNCT07234318

Non-interventional Study to Evaluate the Anti-inflammatory Effects and the Clinical Efficacy of Topical Water Free Cyclosporin 0.1% Eye Drops in Patients With Dry Eye Disease and Associated Ocular Surface Inflammation Non-responding to Artificial Tears

Non-interventional Study to Evaluate the Anti-inflammatory Effects and the Clinical Efficacy of Topical Water Free Cyclosporin 0.1% Eye Drops in Patients With Dry Eye Disease and Associated Ocular Surface Inflammation Non-responding to Artificial Tears: the FOCUS Study

Status
Not Yet Recruiting
Phase
Study type
Observational
Enrollment
25 (estimated)
Sponsor
Laboratoires Thea · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The FOCUS study aims to evaluate the clinical efficacy of 0.1% cyclosporine eye drops solution (Vevizye®, Laboratoires THEA) in patients with moderate to severe dry eye disease characterized by ocular surface inflammation.

Conditions

Interventions

TypeNameDescription
DRUGCyclosporinThis medicinal product contains cyclosporine 0.1% as an active ingredient and pefluorobutylpentane as vehicle.

Timeline

Start date
2025-12-15
Primary completion
2026-03-15
Completion
2026-06-30
First posted
2025-11-18
Last updated
2025-11-18

Source: ClinicalTrials.gov record NCT07234318. Inclusion in this directory is not an endorsement.

Non-interventional Study to Evaluate the Anti-inflammatory Effects and the Clinical Efficacy of Topical Water Free Cyclo (NCT07234318) · Clinical Trials Directory