Phase 3 Safety Study for the Treatment of Presbyopia Subjects

PHASE3CompletedINTERVENTIONAL
Enrollment

362

Participants

Timeline

Start Date

February 21, 2023

Primary Completion Date

February 9, 2024

Study Completion Date

February 9, 2024

Conditions
PresbyopiaNear VisionMiosisEye Diseases
Interventions
DRUG

Aceclidine+Brimonidine combination ophthalmic solution

Combination ophthalmic solution of Aceclidine and Brimonidine

DRUG

Placebo

Placebo: Proprietary Vehicle Solution

DRUG

Aceclidine Ophthalmic Solution

Aceclidine

Trial Locations (36)

16066

Site #312, Cranberry Township

32256

Site #319, Crystal River

32757

Site #309, Mt. Dora

33309

Site #327, San Antonio

36301

Site #326, Dothan

37167

Site #311, Smyrna

38104

Site #315, Memphis

40206

Site #324, Louisville

43065

Site #323, Powell

45242

Site #329, Cincinnati

56308

Site #336, Alexandria

58078

Site #332, West Fargo

58103

Site #310, Fargo

59718

Site #335, Bozeman

61201

Site #317, Rock Island

64154

Site #330, Kansas City

66210

Site #301, Overland Park

66762

Site #307, Pittsburg

78229

Site #318, San Antonio

79902

Site #314, El Paso

80120

Site #308, Littleton

85032

Site #321, Phoenix

85053

Site #328, Phoenix

85202

Site #320, Mesa

85224

Site #302, Chandler

85260

Site #338, Scottsdale

85351

Site #331, Sun City

91204

Site #313, Glendale

92037

Site #334, La Jolla

92663

Site #322, Newport Beach

92843

Site #303, Garden Grove

93105

Site #304, Santa Barbara

94954

Site #306, Petaluma

95670

Site #337, Rancho Cordova

97401

Site #333, Eugene

06810

Site #316, Danbury

Sponsors
All Listed Sponsors
collaborator

ORA, Inc.

INDUSTRY

lead

LENZ Therapeutics, Inc

OTHER

NCT05753189 - Phase 3 Safety Study for the Treatment of Presbyopia Subjects | Biotech Hunter | Biotech Hunter