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Phase 2: VVN461 Ophthalmic Solution for Post -Operative Ocular Inflammation After Cataract Surgery
Sponsor: VivaVision Biotech, Inc
Summary
This is a multicenter, double-masked, randomized, vehicle-controlled, parallel-comparison study conducted at sites in the United States (US) in subjects undergoing routine unilateral cataract extraction and lens replacement (CELR) surgery via phacoemulsification
Official title: A Phase 2, Double-masked, Randomized, Vehicle-controlled Study of VVN461 Ophthalmic Solution in Treating Post -Operative Ocular Inflammation in Subjects Undergoing Routine Unilateral Cataract Surgery
Key Details
Gender
All
Age Range
21 Years - Any
Study Type
INTERVENTIONAL
Enrollment
91
Start Date
2024-01-11
Completion Date
2024-05-15
Last Updated
2026-09-11
Healthy Volunteers
No
Conditions
Interventions
VVN461 Ophthalmic Solution 1.0%
Topical ocular drug
VVN461 Ophthalmic Solution 0.5%
Topical ocular drug
Vehicle
Topical ocular drug
Locations (10)
United Medical Research Institute
Inglewood, California, United States
North Bay Eye Associates
Petaluma, California, United States
Martel Eye Associates
Rancho Cordova, California, United States
ICON Eye Care
Grand Junction, Colorado, United States
Levenson Eye Associates
Jacksonville, Florida, United States
Comprehensive Eye Care, Ltd
Washington, Missouri, United States
Center For Sight - Las Vegas
Las Vegas, Nevada, United States
Cincinnati Eye Institute
Cincinnati, Ohio, United States
Keystone Research
Austin, Texas, United States
Houston Eye Associates
Houston, Texas, United States