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Completed Phase 2 Interventional Results available

Safety and Efficacy of Nyxol With Pilocarpine Eye Drops in Subjects With Presbyopia

ClinicalTrials.gov ID: NCT04675151

Public ClinicalTrials.gov record NCT04675151. 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 Jul 21, 2026, 10:59 PM EDT

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

Official title

Safety and Efficacy of Nyxol (0.75% Phentolamine Ophthalmic Solution) With Pilocarpine Eye Drops in Subjects With Presbyopia

Study identification

NCT ID
NCT04675151
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Ocuphire Pharma, Inc.
Industry
Enrollment
150 participants

Conditions and interventions

Conditions

Interventions

  • Phentolamine Ophthalmic Solution 0.75% Drug
  • Pilocarpine Drug
  • Placebo Other

Drug · Other

Eligibility (public fields only)

Age range
40 Years to 64 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

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

Study timeline

Start date
Feb 14, 2021
Primary completion
May 16, 2021
Completion
Jun 29, 2021
Last update posted
Oct 9, 2025

2021

United States locations

U.S. sites
17
U.S. states
10
U.S. cities
17
Facility City State ZIP Site status
Clinical Site 12 Laguna Hills California 92653
Clinical Site 6 Newport Beach California 92663
Clinical Site 13 Crystal River Florida 34461
Clinical Site 5 Longwood Florida 32779
Clinical Site 11 Maitland Florida 32751
Clinical Site 8 Sarasota Florida 34239
Clinical Site 10 Roswell Georgia 30041
Clinical Site 3 Pittsburg Kansas 66762
Clinical Site 18 St Louis Missouri 63101
Clinical Site 16 Poughkeepsie New York 12603
Clinical Site 14 Fargo North Dakota 58103
Clinical Site 2 Athens Ohio 45701
Clinical Site 9 Cincinnati Ohio 45242
Clinical Site 7 Cleveland Ohio 44115
Clinical Site 15 Powell Ohio 43065
Clinical Site 4 Warwick Rhode Island 02888
Clinical Site 1 Memphis Tennessee 38119

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 NCT04675151, 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 9, 2025 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04675151 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →