RecruitingPhase 2NCT07128628
A Study Evaluating the Safety and Efficacy of a Fixed-Dose Combination for Dry Eye Disease
Studying Medullary sponge kidney
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Bausch & Lomb Incorporated
- Intervention
- Lifitegrast/Perfluorohexyloctane Fixed Dose Combination(drug)
- Enrollment
- 423 target
- Eligibility
- 18 years · All sexes
- Timeline
- 2025 – 2026
Study locations (30)
- Eye Doctors of Arizona, PLLC, Phoenix, Arizona, United States
- Global Research Management, Inc., Glendale, California, United States
- SoCal Eye - Lakewood Clinic, Long Beach, California, United States
- LoBue Laser and Eye Medical Center, Murrieta, California, United States
- Eye Research Foundation, Inc., Newport Beach, California, United States
- Wolstan and Goldberg Eye Associates, Torrance, California, United States
- Segal Drug Trials/Office of Bruce A Segal, MD, Delray Beach, Florida, United States
- Bowden Eye and Associates, Jacksonville, Florida, United States
- Shettle Eye Research, Inc, Largo, Florida, United States
- Clayton Eye Clinical Research, LLC, Morrow, Georgia, United States
- Midwest Cornea Associates LLC, Carmel, Indiana, United States
- Kannarr Eye Care, LLC, Pittsburg, Kansas, United States
- Vance Thompson Vision - Alexandria, Alexandria, Minnesota, United States
- Complete Eye Care of Medina, Medina, Minnesota, United States
- Insight Eyecare Specialties, Inc., Kansas City, Missouri, United States
- +15 more locations on ClinicalTrials.gov
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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