At a glance
ClinicalIndex Comparison RecordPhase 3Completed· 229 enrolled
Drug / intervention
Aceclidine+Brimonidine combination ophthalmic solution +2 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 Multi-Center, Double-Masked Phase 3 Evaluation of the Safety and Efficacy of LNZ101 for the Treatment of Presbyopia
In Brief
A Phase 3 clinical trial evaluating Aceclidine+Brimonidine combination ophthalmic solution, Aceclidine ophthalmic solution, and 1 other intervention for Presbyopia and 3 related conditions. Completed, enrolled 229 participants across 17 sites.
Detailed Summary
Phase 3 Efficacy Study to evaluate the Safety and Efficacy of LNZ100 \& LNZ101 for the Treatment of Presbyopia
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsPresbyopia, Near Vision, Refractive Error, Eye Diseases
CountriesUnited States
Collaborators--
Timeline
Phase 3CompletedFinished
202420252026
First PostedFeb 2023
Enrollment StartMar 2023
Primary CompletionDec 2023
Study CompletionJan 2024
TodayJul 2026
First PostedFeb 15, 2023
Enrollment StartMar 6, 2023
Primary CompletionDec 14, 2023
Study CompletionJan 24, 2024
TodayJul 2, 2026
Enrollment to primary: 9 monthsPosted 3.4 years ago
Interventions
Aceclidine+Brimonidine combination ophthalmic solutiondrug
Aceclidine + Brimonidine combination ophthalmic solution
Aceclidine ophthalmic solutiondrug
Aceclidine ophthalmic solution
Vehicledrug
Proprietary vehicle ophthalmic solution