Status:

COMPLETED

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

Lead Sponsor:

Visus Therapeutics

Conditions:

Presbyopia

Eligibility:

All Genders

45-80 years

Phase:

PHASE2

Brief Summary

Safety and Efficacy Study of BRIMOCHOL™ vs. BRIMOCHOL™ F vs. Carbachol Monotherapy Topical Ophthalmic Solutions in Subjects with Emmetropic Phakic and Pseudophakic Presbyopia

Detailed Description

A 3-Dose, Multicenter, Randomized, Double-Masked, Crossover Phase 2 Safety and Efficacy Study of BRIMOCHOL™ Topical Ophthalmic Solution vs. BRIMOCHOL™ F Topical Ophthalmic Solution vs. Monotherapy wit...

Eligibility Criteria

Inclusion

  • Male or female in good general health
  • Must have presbyopia

Exclusion

  • History of allergic reaction to the study drug or any of its components
  • Any disease or medical condition that, in the opinion of the Investigator, would prevent the subject from participating in the study or might confound study results

Key Trial Info

Start Date :

March 24 2021

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

October 19 2021

Estimated Enrollment :

18 Patients enrolled

Trial Details

Trial ID

NCT04774237

Start Date

March 24 2021

End Date

October 19 2021

Last Update

February 5 2025

Active Locations (3)

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Page 1 of 1 (3 locations)

1

Global Research Management, Inc.

Glendale, California, United States, 91204

2

Eye Research Foundation

Newport Beach, California, United States, 92663

3

Total Eye Care, PA

Memphis, Tennessee, United States, 38119

Safety and Efficacy Study of BRIMOCHOL™, BRIMOCHOL™ F, and Carbachol in Subjects With Emmetropic Phakic and Pseudophakic Presbyopia | DecenTrialz