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Completed Phase 3 Interventional Accepts healthy volunteers Results available

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

ClinicalTrials.gov ID: NCT05270863

Public ClinicalTrials.gov record NCT05270863. 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 23, 2026, 8:41 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
NCT05270863
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Visus Therapeutics
Other
Enrollment
182 participants

Conditions and interventions

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 30, 2022 (Actual)
Primary completion
Mar 17, 2023 (Actual)
Completion
Apr 10, 2023 (Actual)
Last update posted
Oct 15, 2024

2022 – 2023

United States locations

U.S. sites
15
U.S. states
9
U.S. cities
13
Facility City State ZIP Site status
Visus Therapeutics Investigative Site Glendale California 91204 —
Visus Therapeutics Investigative Site Rancho Cordova California 95670 —
Visus Therapeutics Investigative Site Jacksonville Florida 32204 —
Visus Therapeutics Investigative Site Morrow Georgia 30260 —
Visus Therapeutics Investigative Site Roswell Georgia 30076 —
Visus Therapeutics Investigative Site Shawnee Mission Kansas 66204 —
Visus Therapeutics Investigative Site Kansas City Missouri 64133 —
Visus Therapeutics Investigative Site Kansas City Missouri 64154 —
Visus Therapeutics Investigative Site Pittsburgh Pennsylvania 66762 —
Visus Therapeutics Investigative Site Memphis Tennessee 38119 —
Visus Therapeutics Investigative Site Memphis Tennessee 77027 —
Visus Therapeutics Investigative Site Cedar Park Texas 78613 —
Visus Therapeutics Investigative Site Houston Texas 77027 —
Visus Therapeutics Investigative Site San Antonio Texas 78229 —
Visus Therapeutics Investigative Site Ogden Utah 84403 —

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 NCT05270863, 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 Oct 15, 2024 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05270863 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →