At a glance
ClinicalIndex Comparison RecordPhase 3Completed· 362 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.
Safety Study: A Multi-Center, Double-Masked Phase 3 Safety Study Evaluation of the Long-Term Safety of LNZ101 in Presbyopic Subjects
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 362 participants across 40 sites.
Detailed Summary
Safety Study of the Long-Term Safety of LNZ100 \& LNZ101 in Presbyopic Subjects
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsPresbyopia, Near Vision, Refractive Error, Eye Diseases
CountriesUnited States
Collaborators--
Timeline
Phase 3CompletedFinished
202420252026
Enrollment StartFeb 2023
First PostedMar 2023
Primary CompletionFeb 2024
TodayJul 2026
First PostedMar 3, 2023
Enrollment StartFeb 21, 2023
Primary CompletionFeb 9, 2024
TodayJul 2, 2026
Enrollment to primary: 12 monthsPosted 3.3 years ago
Interventions
Aceclidine+Brimonidine combination ophthalmic solutiondrug
Aceclidine + Brimonidine combination ophthalmic solution
Aceclidine ophthalmic solutiondrug
Aceclidine ophthalmic solution
Vehicledrug
Vehicle