Ozmosi | Aceclidine Drug Profile
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Aceclidine

Pronounced as: ay-SEH-kli-deen

Alternative Names: aceclidine
Clinical Status: Active
Latest Update: 2026-05-13
Latest Update Note: Clinical Trial Update

Product Description

Aceclidine has been marketed in Europe but has not been used clinically in the United States. It is used in the treatment of open-angle glaucoma and is a parasympathomimetic agent.

Mechanisms of Action: mAChR Agonist

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: Ophthalmic

FDA Designation: *

Approval Status: Approved

Approved Countries: Germany | Greece | Italy | Peru | Portugal

Approved Indications: None

Company: LENZ Therapeutics
Company Location: Western America
Company Founding Year: 2020
Additional Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Aceclidine

Countries in Clinic: China, United States

Active Clinical Trial Count: 4

Recent & Upcoming Milestones

Highest Development Phases

Phase 3: Miosis|Presbyopia

Trial ID

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

NCT06045299

JX07001

P3

Completed

Presbyopia|Miosis

2024-08-19

14%

2025-03-04

Primary Endpoints

CTR20240460

CTR20240460

P1

Completed

Presbyopia

2024-04-10

12%

2025-04-29

Patient Enrollment|Primary Completion Date|Start Date|Study Completion Date|Treatments|Trial Status

NCT06270030

JX07002

P1

Completed

Presbyopia

2024-04-10

12%

2025-08-27

Primary Endpoints

NCT05753189

Safety Study

P3

Completed

Miosis|Presbyopia

2024-02-09

13%

2026-05-14

Primary Endpoints|Treatments