Ozmosi | Apraclonidine Drug Profile
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Apraclonidine

Alternative Names: apraclonidine, iopidine
Clinical Status: Inactive
Latest Update: 2025-01-14
Latest Update Note: Clinical Trial Update

Product Description

Mechanisms of Action: ADRA2A Agonist

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: N/A

FDA Designation: *

Approval Status: Approved

Approved Countries: Australia | Austria | Belgium | Canada | Chile | Colombia | Denmark | Egypt | Finland | France | Germany | Greece | India | Ireland | Israel | Italy | Korea | Luxembourg | Malta | Morocco | Netherlands | New Zealand | Norway | Peru | Portugal | Slovenia | South Africa | Spain | Sweden | Switzerland | Turkey | United Kingdom | United States | Venezuela

Approved Indications: None

Known Adverse Events: None

Company: Alcon
Company Location:
Company CEO:
Additional Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Apraclonidine

Countries in Clinic: United States

Active Clinical Trial Count: 1

Recent & Upcoming Milestones

Highest Development Phases

Phase 3: Erythema

Trial ID

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

NCT06444529

 DEW422-C001

P3

Completed

Erythema

2024-11-14

4%

2025-01-15

Primary Endpoints|Study Completion Date

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Date

Type

Title

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