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Completed Phase 3 Interventional Results available

An Evaluation of the Efficacy and Safety of CSF-1 in the Temporary Correction of Presbyopia (NEAR-1)

ClinicalTrials.gov ID: NCT04599933

Public ClinicalTrials.gov record NCT04599933. 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 Oct 21, 2026, 4:27 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

A Multi-Center, Double-Masked, Vehicle-Controlled, Evaluation of the Efficacy and Safety of CSF-1 in the Temporary Correction of Presbyopia (the NEAR-1 Study: Near Eye-vision Acuity Restoration)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a 4-visit, multi-center, randomized, double-masked, vehicle-controlled study evaluating the safety and efficacy of CSF-1 in the temporary correction of presbyopia.

Study identification

NCT ID
NCT04599933
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Orasis Pharmaceuticals Ltd.
Industry
Enrollment
309 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
45 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
Oct 18, 2020 (Actual)
Primary completion
Feb 11, 2022 (Actual)
Completion
Feb 19, 2022 (Actual)
Last update posted
Apr 4, 2024

2020 – 2022

United States locations

U.S. sites
17
U.S. states
13
U.S. cities
17
Facility City State ZIP Site status
Orasis Investigative Site Sun City Arizona 85351 —
Orasis Investigative Site Glendale California 91204 —
Orasis Investigative Site Los Angeles California 90013 —
Orasis Investigative Site Fort Myers Florida 33901 —
Orasis Investigative Site Mt. Dora Florida 32757 —
Orasis Investigative Site Morrow Georgia 30260 —
Orasis Investigative Site Overland Park Kansas 66210 —
Orasis Investigative Site Louisville Kentucky 40206 —
Orasis Investigative Site Kansas City Missouri 64133 —
Orasis Investigative Site St Louis Missouri 63131 —
Orasis Investigative Site Henderson Nevada 89052 —
Orasis Investigative Site Elizabeth City North Carolina 27909 —
Orasis Investigative Site Cranberry Township Pennsylvania 16066 —
Orasis Investigative Site Wilkes-Barre Pennsylvania 18702 —
Orasis Investigative Site Rapid City South Dakota 57701 —
Orasis Investigative Site Memphis Tennessee 38119 —
Orasis Investigative Site El Paso Texas 79902 —

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 NCT04599933, 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 Apr 4, 2024 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04599933 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →