100
Participants
Start Date
July 2, 2025
Primary Completion Date
January 31, 2026
Study Completion Date
January 31, 2026
Perfluorohexyloctane ophthalmic solution
Eligible subjects will receive Miebo up to 4 times bilaterally on Day 1/Visit 1 (1 drop instilled bilaterally by site staff in-clinic while wearing contact lenses and the rest self-administered throughout the remainder of the day while wearing contact lenses). Starting on Day 2, subjects will self-administer the first drop of Miebo bilaterally before inserting contact lenses for the day. Subjects will wait 30 minutes after the first dose of Miebo to insert their contact lenses and will then instill 3 additional drops of Miebo while wearing contact lenses approximately evenly spaced throughout the rest of the day. Subjects will continue to self-administer Miebo QID bilaterally following the dosing schedule from Day 2 for approximately 30 days. Subjects are expected to record daily VAS assessments throughout the study. The VAS assessments will be collected by the sites at Visits 2, 3, and 4.
Site 108, Vestal
Site 107, Longwood
Site 106, Nashville
Site 103, Athens
Site 102, Medina
Site 104, Pittsburg
Site 101, San Diego
Site 105, San Francisco
Bausch & Lomb Incorporated
INDUSTRY