Andover, MA
Andover, Massachusetts, 01810, United States
NCT Number: NCT02974907
The objective of this study is to compare the safety and efficacy of RGN-259 Ophthalmic Solutions to placebo for the treatment of the signs and symptoms of dry eye.
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Notify Me18 year and older
All sexes
Interventional
Phase 3
Andover, Massachusetts, 01810, United States
Dry eye can be caused by many variable factors. Some examples include hormonal changes due to aging, or living in an environment of low humidity for long periods of time. Dry eye is a complex disease that may result in symptoms like discomfort, visual disturbance, and dryness. Patients with dry eye often have damage on the surface of the eye. In previous studies, RGN-259 has been shown to promote healing of the surface of the eye and decrease inflammation. It suggests that RGN-259 has a significant potential to be an important new safe and effective therapeutic in the treatment of dry eye syndrome.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
A preservative-free, sterile eye drop solution containing Tβ4 for direct instillation into each eye, four times a day (QID) for 28 days
Other names: Tβ4, Thymosin Beta 4
It is composed of the same excipients as RGN-259 but does not contain Tβ4
Other names: Vehicle Control
Time frame: 29 days after first dosing
Change from Baseline at Day 29 using the Ora Calibra® Ocular Discomfort Scale (6-point scale where 0 = none and 5 = worst)
Time frame: 29 days after first dosing
Change from Baseline at Day 29 using the Ora Calibra® scale (5-point scale with half (0.5) increments where 0 = none and 4 = severe)
Time frame: 8, 15, 29 days after first dosing
Comparing each of active group & Placebo.
Time frame: 29 days after first dosing
Comparing each of active group & Placebo.
Time frame: 8, 15, 29 days after first dosing
Comparing each of active group & Placebo.
Time frame: 8, 15, 29 days after first dosing
Comparing each of active group & Placebo.
Time frame: 1, 8, 15, 29 days
Change or shifts from Baseline
Time frame: 1, 8, 15, 29 days
Change or shifts from Baseline
Time frame: 1, 8, 15, 29 days
Frequencies
Time frame: 1, 29 days
Change or shifts from Baseline
ReGenTree, LLC
Industry
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-2
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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