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Reproxalap Ophthalmic Solution (0.25%) for Dry Eye Syndrome
Phase 2
Waitlist Available
Research Sponsored by Aldeyra Therapeutics, Inc.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up on the first day of two consecutive dosing days for both crossover periods
Awards & highlights
Study Summary
This trial will compare the efficacy and safety of a new eye drop, Reproxalap, to a placebo drop in people with dry eye disease.
Eligible Conditions
- Dry Eye Syndrome
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ on the second day of two consecutive dosing days for both crossover periods
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~on the second day of two consecutive dosing days for both crossover periods
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Change from baseline in conjunctival redness in a dry eye chamber
Schirmer's test mean change from baseline
Secondary outcome measures
Schirmer's test ≥10mm responder analysis of change from baseline
Side effects data
From 2021 Phase 2 trial • 158 Patients • NCT049710314%
General disorders and administration site conditions
100%
80%
60%
40%
20%
0%
Study treatment Arm
Vehicle
Reproxalap (0.25%)
Trial Design
2Treatment groups
Experimental Treatment
Placebo Group
Group I: Reproxalap Ophthalmic Solution (0.25%)Experimental Treatment1 Intervention
Group II: Vehicle Ophthalmic SolutionPlacebo Group1 Intervention
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Reproxalap Ophthalmic Solution (0.25%)
2022
Completed Phase 3
~2690
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Who is running the clinical trial?
Aldeyra Therapeutics, Inc.Lead Sponsor
29 Previous Clinical Trials
3,970 Total Patients Enrolled
Frequently Asked Questions
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