Geneva, Aug. 29 -- International Clinical Trials Registry received information related to the study (NCT07111013) titled 'A Study to Assess the Long-Term Safety of Lifitegrast/Perfluorohexyloctane Fixed-Dose Combination in Subjects With Dry Eye Disease' on Aug. 6.
Study Type: Interventional
Study Design:
Allocation: N/A. Intervention model: Single Group Assignment. Primary purpose: Treatment. Masking: None (Open Label).
Primary Sponsor: Bausch & Lomb Incorporated
Condition:
Dry Eye Disease
Intervention:
Drug: Lifitegrast/perfluorohexyloctane (PFHO)
Recruitment Status: Not recruiting
Phase: Phase 3
Date of First Enrollment: December 2025
Target Sample Size: 150
To know more, visit https://clinicaltrials.gov/ct2/show/NCT071...