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COMPLETED
NCT06164743
PHASE2

Phase 2: VVN461 Ophthalmic Solution for Post -Operative Ocular Inflammation After Cataract Surgery

Sponsor: VivaVision Biotech, Inc

View on ClinicalTrials.gov

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

DRUG

VVN461 Ophthalmic Solution 1.0%

Topical ocular drug

DRUG

VVN461 Ophthalmic Solution 0.5%

Topical ocular drug

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