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Completed Phase 3 Interventional Accepts healthy volunteers Results available

Phase 3 Evaluation of the Safety and Efficacy of LNZ100 & LNZ101 for the Treatment of Presbyopia

ClinicalTrials.gov ID: NCT05656027

Public ClinicalTrials.gov record NCT05656027. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 18, 2026, 1:36 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multi-Center, Double-Masked Phase 3 Evaluation of the Safety and Efficacy of LNZ101 for the Treatment of Presbyopia

Study identification

NCT ID
NCT05656027
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
LENZ Therapeutics, Inc
Other
Enrollment
469 participants

Conditions and interventions

Interventions

  • Aceclidine ophthalmic solution Drug
  • Aceclidine+Brimonidine combination ophthalmic solution Drug
  • Brimonidine Drug

Drug

Eligibility (public fields only)

Age range
45 Years to 75 Years
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 18, 2022
Primary completion
Dec 14, 2023
Completion
Jan 24, 2024
Last update posted
May 12, 2026

2022 – 2024

United States locations

U.S. sites
25
U.S. states
11
U.S. cities
23
Facility City State ZIP Site status
Site #106 Chandler Arizona 85224
Site #121 Mesa Arizona 85202
Site #122 Phoenix Arizona 85032
Site #124 Phoenix Arizona 85053
Site #128 Scottsdale Arizona 85260
Site #125 Sun City Arizona 85351
Site #130 Azusa California 91702
Site #110 Garden Grove California 92843
Site #101 Glendale California 91204
Site #129 Newport Beach California 92663
Site #107 Petaluma California 94954
Site #126 Rancho Cordova California 95670
Site #111 Santa Barbara California 93105
Site #109 Littleton Colorado 80120
Site #102 Mt. Dora Florida 32757
Site #118 Rock Island Illinois 61201
Site #127 Overland Park Kansas 66210
Site #108 Pittsburg Kansas 66762
Site #131 Rochester New York 14618
Site #104 Fargo North Dakota 58103
Site #103 Kingston Pennsylvania 18704
Site #116 Memphis Tennessee 38104
Site #112 Smyrna Tennessee 37167
Site #119 San Antonio Texas 78229
Site #123 San Antonio Texas 78229

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05656027, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted May 12, 2026 · Synced May 18, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05656027 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →