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Completed Phase 3 Interventional Results available

Assessment of the Safety and Efficacy of RGN-259 Ophthalmic Solutions for Dry Eye Syndrome: ARISE-3

ClinicalTrials.gov ID: NCT03937882

Public ClinicalTrials.gov record NCT03937882. 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 22, 2026, 11:58 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, Randomized, Double Masked, Placebo Controlled Clinical Study to Assess the Safety and Efficacy of RGN-259 Ophthalmic Solutions for the Treatment of Dry Eye (ARISE-3)

Brief summary

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

The objective of this study is to compare the safety and efficacy of RGN-259 Ophthalmic Solution to placebo for the treatment of the signs and symptoms of dry eye.

Study identification

NCT ID
NCT03937882
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
ReGenTree, LLC
Industry
Enrollment
700 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
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
May 24, 2019 (Actual)
Primary completion
Nov 8, 2020 (Actual)
Completion
Oct 7, 2021 (Actual)
Last update posted
Aug 28, 2026

2019 – 2021

United States locations

U.S. sites
20
U.S. states
16
U.S. cities
19
Facility City State ZIP Site status
Cornea and Cataract Consultants of Arizona Phoenix Arizona 85032 —
Eye Research Foundation Newport Beach California 92663 —
Vision Institute Colorado Springs Colorado 80907 —
Dovilan Wyatt MD, LLC Chicago Illinois 60619 —
Whitson Vision Indianapolis Indiana 46240 —
Midwest Cornea Associates, LLC Indianapolis Indiana 46290 —
The Eye Care Institute Louisville Kentucky 40206 —
Andover Eye Associates Andover Massachusetts 01810 —
Andover Eye Associates Raynham Massachusetts 02767 —
Center For Sight Henderson Nevada 89052 —
Oculus Research, Inc. at the Eye Care Center Raleigh North Carolina 27603 —
Visual Eyes Optometric Shelby North Carolina 28150 —
Bergstrom Eye Research, LLC Fargo North Dakota 58103 —
Scott & Christie and Associates, PC Cranberry Township Pennsylvania 16066 —
Andover Eye Associates Warwick Rhode Island 02886 —
Total Eye Care, P.A. Memphis Tennessee 38119 —
Texan Eye/Keystone Research Austin Texas 78731 —
Mountain View Eye Center Layton Utah 84041 —
Country Hills Eye Center Ogden Utah 84403 —
Piedmont Eye Center Lynchburg Virginia 24502 —

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 NCT03937882, 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 Aug 28, 2026 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03937882 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →