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NCT03937882 · ClinicalTrials.gov registry record · Phase 3

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

A Phase 3 study, sponsored by ReGenTree.

Completed
Registry status
Phase 3
Development phase
700
Enrollment target

NCT03937882: Completed Phase 3 study, sponsored by ReGenTree.

NCT03937882 is a Phase 3 study that has completed, run by ReGenTree. The registered enrollment target is 700 participants, roughly in line with the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03937882, a Phase 3 study, has completed, sponsored by ReGenTree.

COMPLETED
Registry status
Phase 3
Development phase
700 participants
Enrollment target

Study Summary

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.

Primary Outcome

Inferior corneal staining was assessed using the Ora Calibra® Corneal and Conjunctival Staining Scale, which is a 0 to 4 scale and where higher numbers indicating more severe staining.

Interventions

  • DRUG Placebo
  • DRUG RGN-259

Trial Details

FieldValue
Enrollment Target 700 participants
Start Date 2019-05-24
Est. Completion 2021-10-07
Phase Phase 3
ReGenTree

6 total trials

What the finished NCT03937882 record still lists

NCT03937882 is an interventional study that assigns participants to a tested intervention. The registered 700 participants enrollment target is mid-sized for trials with a published cap, roughly in line with the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target.

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT03937882 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03937882 about?

NCT03937882 is a clinical study titled "Assessment of the Safety and Efficacy of RGN-259 Ophthalmic Solutions for Dry Eye Syndrome: ARISE-3". 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.

What is the current status of trial NCT03937882?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 700 participants. The study started on 2019-05-24. Estimated completion is 2021-10-07.

What interventions are being tested in trial NCT03937882?

The interventions under investigation include: Placebo (DRUG), RGN-259 (DRUG).

Who is sponsoring clinical trial NCT03937882?

This trial is sponsored by ReGenTree, which has 6 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03937882's enrollment target sits among peer trials

700 506th of 2000 higher than 1,485 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT03937882, the US trial registry maintained by the National Library of Medicine. NCT03937882 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.