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NCT07140783 · ClinicalTrials.gov registry record · Phase 3

OPI-NXYDLD-303 Safety and Efficacy of Phentolamine Ophthalmic Solution in Keratorefractive Surgery Participants With Decreased Mesopic Visual Acuity

A Phase 3 study of Vision Disorders and Vision Loss Night, sponsored by Ocuphire Pharma.

Recruiting
Registry status
Phase 3
Development phase
200
Enrollment target
20
Study locations

NCT07140783: Recruiting Phase 3 study of Vision Disorders and Vision Loss Night, sponsored by Ocuphire Pharma.

NCT07140783 is a Phase 3 study of Vision Disorders and Vision Loss Night that is actively recruiting participants, run by Ocuphire Pharma. The registered enrollment target is 200 participants, above the 34-participant average among 5 other Vision Disorders trials with a reported enrollment target (488% higher). The trial reports 20 study locations across 7 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07140783, a Phase 3 study of Vision Disorders and Vision Loss Night, is actively recruiting participants, sponsored by Ocuphire Pharma.

RECRUITING
Registry status
Phase 3
Development phase
200 participants
Enrollment target
20
Study locations

Study Summary

The goal of this clinical trial is to learn if Phentolamine Ophthalmic Solution works to treat adults that have had keratorefractive surgery and have decreased visual acuity under mesopic conditions. It will also learn about the safety of Phentolamine Ophthalmic Solution. The main questions it aims to answer are: Researchers will compare Phentolamine Ophthalmic Solution to a placebo (a look-alike substance that contains no drug) to see if Phentolamine Ophthalmic Solution works to improve vision in low light conditions. Participants will: Take Phentolamine Ophthalmic Solution or a placebo drop every day for 2 weeks Visit the clinic once every week for 2 weeks for checkups and tests Keep a diary of when they instill the study medication each evening

Primary Outcome

To evaluate the efficacy of POS to improve mLCVA in subjects with previous keratorefractive surgery

Interventions

  • DRUG Placebo
  • DRUG 0.75% Phentolamine Ophthalmic Solution

Study Locations (20)

California

  • Global Research Management - Glendale
  • Gordon Schanzlin New Vision - La Jolla
  • Eye Research Foundation - Newport Beach
  • California Eye Specialists Medical Group - Pasadena
  • NVISION Clinical Research - San Diego
  • Scripps Poway Eyecare and Optometry - San Diego
  • Wolsten and Goldberg Eye Assoc. - Torrance

Arizona

  • Arizona Eye Care - Chandler
  • Carrot Eye Center - Mesa
  • Eye Doctors of Arizona - Phoenix
  • MRB Eye Care Consultants - Scottsdale

Florida

  • Glaucoma Specialist of South Florida - Delray Beach
  • Segal Drug Trials - Delray Beach

Illinois

  • Wyse Eyecare - Northbrook
  • Virdi Eye Clinic - Rock Island

Kansas

  • Durrie Vision - Overland Park
  • Kannarr Eye Care - Pittsburg

Massachusetts

  • Eye Health Vision Center - South Dartmouth
  • Northeast Eye Research Associates - Woburn

North Carolina

  • Oculus Research - Garner

Trial Details

FieldValue
Enrollment Target 200 participants
Start Date 2025-09-02
Est. Completion 2026-03
Phase Phase 3
Ocuphire Pharma

14 total trials

What NCT07140783 shows while recruiting

NCT07140783 is an interventional study that assigns participants to a tested intervention. The registered 200 participants enrollment target is mid-sized for trials with a published cap, above the 34-participant average among 5 other Vision Disorders trials with a reported enrollment target (488% higher).

The record links to 2 conditions, with Vision Disorders appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT07140783 names 20 study sites across 7 states, led by California, Arizona, Florida.

Frequently Asked Questions

What is clinical trial NCT07140783 about?

NCT07140783 is a clinical study titled "OPI-NXYDLD-303 Safety and Efficacy of Phentolamine Ophthalmic Solution in Keratorefractive Surgery Participants With Decreased Mesopic Visual Acuity". The goal of this clinical trial is to learn if Phentolamine Ophthalmic Solution works to treat adults that have had keratorefractive surgery and have decreased visual acuity under mesopic conditions. It will also learn about the safety of Phentolamine Ophthalmic Solution. The main questions it aims ...

What is the current status of trial NCT07140783?

This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 200 participants. The study started on 2025-09-02. Estimated completion is 2026-03.

What conditions does trial NCT07140783 study?

This clinical trial studies the following conditions: Vision Disorders, Vision Loss Night.

What interventions are being tested in trial NCT07140783?

The interventions under investigation include: Placebo (DRUG), 0.75% Phentolamine Ophthalmic Solution (DRUG).

Who is sponsoring clinical trial NCT07140783?

This trial is sponsored by Ocuphire Pharma, which has 14 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07140783 being conducted?

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

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Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

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Source: ClinicalTrials.gov NCT07140783, the US trial registry maintained by the National Library of Medicine. NCT07140783 (mid enrollment · wide site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.