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Completed Phase 3 Interventional Accepts healthy volunteers

Safety and Efficacy Study of BRIMOCHOL™ PF and Carbachol PF in Subjects With Emmetropic Phakic and Pseudophakic Presbyopia

ClinicalTrials.gov ID: NCT05135286

Public ClinicalTrials.gov record NCT05135286. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 17, 2026, 11:30 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Multicenter, Double-Masked, Randomized, Safety and Efficacy Study of BRIMOCHOL™ PF and Carbachol PF Topical Ophthalmic Solution With Emmetropic Phakic and Pseudophakic Presbyopia

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Safety and Efficacy Study of BRIMOCHOL™ PF and Carbachol PF in Subjects With Emmetropic Phakic and Pseudophakic Presbyopia

Study identification

NCT ID
NCT05135286
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Visus Therapeutics
Other
Enrollment
629 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
45 Years to 80 Years
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 15, 2022 (Actual)
Primary completion
Mar 13, 2025 (Actual)
Completion
Mar 13, 2025 (Actual)
Last update posted
Aug 6, 2025

2022 – 2025

United States locations

U.S. sites
42
U.S. states
22
U.S. cities
42
Facility City State ZIP Site status
Visus Therapeutics Investigative Site Chandler Arizona 85224 —
Visus Therapeutics Investigative Site Phoenix Arizona 85032 —
Visus Therapeutics Investigative Site Sun City Arizona 85351 —
Visus Therapeutics Investigative Site Glendale California 91204 —
Visus Therapeutics Investigative Site Inglewood California 90301 —
Visus Therapeutics Investigative Site Irvine California 92604 —
Visus Therapeutics Investigative Site Mission Hills California 91345 —
Visus Therapeutics Investigative Site Newport Beach California 92663 —
Visus Therapeutics Investigative Site Pasadena California 91107 —
Visus Therapeutics Investigative Site Santa Barbara California 93105 —
Visus Therapeutics Investigative Site Littleton Colorado 80120 —
Visus Therapeutics Investigative Site Danbury Connecticut 06810 —
Visus Therapeutics Investigative Site Crystal River Florida 34429 —
Visus Therapeutics Investigative Site Delray Beach Florida 33484 —
Visus Therapeutics Investigative Site Fort Lauderdale Florida 33309 —
Visus Therapeutics Investigative Site Jacksonville Florida 32256 —
Visus Therapeutics Investigative Site Largo Florida 33770 —
Visus Therapeutics Investigative Site Mt. Dora Florida 32757 —
Visus Therapeutics Investigative Site Lake Villa Illinois 60046 —
Visus Therapeutics Investigative Site Indianapolis Indiana 46260 —
Visus Therapeutics Investigative Site Louisville Kentucky 40206 —
Visus Therapeutics Investigative Site Bloomington Minnesota 55420 —
Visus Therapeutics Investigative Site Kansas City Missouri 64111 —
Visus Therapeutics Investigative Site St Louis Missouri 63128 —
Visus Therapeutics Investigative Site Henderson Nevada 89502 —
Visus Therapeutics Investigative Site Poughkeepsie New York 12603 —
Visus Therapeutics Investigative Site Garner North Carolina 27529 —
Visus Therapeutics Investigative Site West Fargo North Dakota 58078 —
Visus Therapeutics Investigative Site Powell Ohio 43065 —
Visus Therapeutics Investigative Site Portland Oregon 97210 —
Visus Therapeutics Investigative Site Cranberry Township Pennsylvania 16066 —
Visus Therapeutics Investigative Site Wilkes-Barre Pennsylvania 18702 —
Visus Therapeutics Investigative Site Sioux Falls South Dakota 57108 —
Visus Therapeutics Investigative Site Maryville Tennessee 37803 —
Visus Therapeutics Investigative Site Memphis Tennessee 38119 —
Visus Therapeutics Investigative Site Smyrna Tennessee 37167 —
Visus Therapeutics Investigative Site Hurst Texas 76054 —
Visus Therapeutics Investigative Site Lakeway Texas 78738 —
Visus Therapeutics Investigative Site San Antonio Texas 78229 —
Visus Therapeutics Investigative Site Draper Utah 84020 —
Visus Therapeutics Investigative Site Falls Church Virginia 22046 —
Visus Therapeutics Investigative Site Lynchburg Virginia 24502 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05135286, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 6, 2025 · Synced Oct 17, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05135286 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →