At a glance
ClinicalIndex Comparison RecordPhase 3Completed· 123 enrolled
Drug / intervention
ADX-102 Ophthalmic Solution (0.5%) +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
A Phase 3, Randomized, Double-masked, Vehicle-controlled Trial to Evaluate the Safety and Efficacy of ADX-102 Ophthalmic Solution in Subjects With Non-infectious Anterior-uveitis.
In Brief
A Phase 3 clinical trial evaluating ADX-102 Ophthalmic Solution (0.5%) and Vehicle of ADX-102 Ophthalmic Solution for Non-infectious Anterior Uveitis. Completed, enrolled 123 participants across 27 sites.
Detailed Summary
A Phase 3, randomized, double-masked, vehicle-controlled trial to evaluate the safety and efficacy of ADX-102 ophthalmic solution in Subjects with non-infectious anterior-uveitis.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsNon-infectious Anterior Uveitis
CountriesUnited States
Collaborators--
Timeline
Phase 3CompletedFinished
201820192020202120222023202420252026
Enrollment StartApr 2017
First PostedApr 2017
Primary CompletionApr 2019
Study CompletionApr 2019
TodayJul 2026
First PostedApr 27, 2017
Enrollment StartApr 26, 2017
Primary CompletionApr 19, 2019
Study CompletionApr 26, 2019
TodayJul 2, 2026
Enrollment to primary: 2.0 yearsPosted 9.2 years ago
Interventions
ADX-102 Ophthalmic Solution (0.5%)drug
ADX-102 Ophthalmic Solution (0.5%) administered for approximately four weeks.
Vehicle of ADX-102 Ophthalmic Solutiondrug
Vehicle of ADX-102 Ophthalmic Solution administered for approximately four weeks.