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

Completed · Phase 2

Conditions studied: Inflammation

In brief

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

Key facts

Study ID

NCT06164743

Run by

VivaVision Biotech, Inc

People needed

91

Starts

2024-01-11

Expected to finish

2024-05-15

Last updated by the study team

2025-06-10

Who can join

Age: 21 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• ≥21 years of age and in good general health at Visit 1 (Screening)
• Willing and able to provide informed consent and provide relevant privacy authorization(s)
• Willing and able to comply with study requirements and visit schedule
• Clear ocular media (other than cataract) in the study eye
• Planning to undergo routine unilateral cataract surgery via phacoemulsification extraction and implantation of an intraocular lens.

You may not qualify if…

• Any ocular pain at Visit 1 (Screening)
• Recent use of corticosteroids or oral non-steroidal anti-inflammatory drugs

Where it is running

• 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

Full record on ClinicalTrials.gov

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