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COMPLETED Phase 3

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

NCT05135286 · View on ClinicalTrials.gov ↗

Study Summary

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

Conditions Studied

Interventions

  • DRUG Vehicle
  • DRUG BRIMOCHOL™ PF
  • DRUG Carbachol PF

Study Locations (20)

California

  • Visus Therapeutics Investigative Site — Glendale
  • Visus Therapeutics Investigative Site — Inglewood
  • Visus Therapeutics Investigative Site — Irvine
  • Visus Therapeutics Investigative Site — Mission Hills
  • Visus Therapeutics Investigative Site — Newport Beach
  • Visus Therapeutics Investigative Site — Pasadena
  • Visus Therapeutics Investigative Site — Santa Barbara

Florida

  • Visus Therapeutics Investigative Site — Crystal River
  • Visus Therapeutics Investigative Site — Delray Beach
  • Visus Therapeutics Investigative Site — Fort Lauderdale
  • Visus Therapeutics Investigative Site — Jacksonville
  • Visus Therapeutics Investigative Site — Largo
  • Visus Therapeutics Investigative Site — Mt. Dora

Arizona

  • Visus Therapeutics Investigative Site — Chandler
  • Visus Therapeutics Investigative Site — Phoenix
  • Visus Therapeutics Investigative Site — Sun City

Colorado

  • Visus Therapeutics Investigative Site — Littleton

Connecticut

  • Visus Therapeutics Investigative Site — Danbury

Illinois

  • Visus Therapeutics Investigative Site — Lake Villa

Indiana

  • Visus Therapeutics Investigative Site — Indianapolis

Trial Details

FieldValue
Enrollment Target 629 participants
Start Date 2022-03-15
Est. Completion 2025-03-13
Phase Phase 3

Sponsor

Visus Therapeutics

1 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05135286

The ClinicalTrials.gov registry entry for NCT05135286 describes a study currently listed as completed. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 629 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Visus Therapeutics, which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Presbyopia appearing as the primary indexed condition, and to 3 interventions — of which Vehicle is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT05135286 reports 20 study locations spanning 7 distinct geographic areas — top geographies include California, Florida, Arizona. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT05135286 about?

NCT05135286 is a clinical study titled "Safety and Efficacy Study of BRIMOCHOL™ PF and Carbachol PF in Subjects With Emmetropic Phakic and Pseudophakic Presbyopia". Safety and Efficacy Study of BRIMOCHOL™ PF and Carbachol PF in Subjects With Emmetropic Phakic and Pseudophakic Presbyopia

What is the current status of trial NCT05135286?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 629 participants. The study started on 2022-03-15. Estimated completion is 2025-03-13.

What conditions does trial NCT05135286 study?

This clinical trial studies the following conditions: Presbyopia. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT05135286?

The interventions under investigation include: Vehicle (DRUG), BRIMOCHOL™ PF (DRUG), Carbachol PF (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT05135286?

This trial is sponsored by Visus Therapeutics, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT05135286 being conducted?

This trial has 20 study locations across Arizona, California, Colorado, Connecticut, Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial