Evaluate Efficacy and Safety of POS to Improve Distance-corrected Near Visual in Participants With Presbyopia
NCT06542497 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 569
Last updated 2026-03-12
Summary
Safety and efficacy of POS in participants with presbyopia
Conditions
Interventions
- DRUG
-
0.75% phentolamine ophthalmic solution
Once daily dosing
- DRUG
-
Once daily dosing
Sponsors & Collaborators
-
Ocuphire Pharma, Inc.
lead INDUSTRY
Principal Investigators
-
Jay V Pepose, MD · Ocuphire Pharma
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- TRIPLE
- Model
- PARALLEL
Eligibility
- Min Age
- 45 Years
- Max Age
- 64 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2024-08-15
- Primary Completion
- 2025-04-03
- Completion
- 2026-01-22
- FDA Drug
- Yes
Countries
- United States
Study Locations
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