Ozmosi | OCU-200 Drug Profile
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OCU-200

Alternative Names: ocu-200, ocu 200, ocu200
Clinical Status: Active
Latest Update: 2025-12-03
Latest Update Note: Clinical Trial Update

Product Description

OCU200 is a biologic product candidate in preclinical development for treating severely sight-threatening diseases like Diabetic Macular Edema (DME), Diabetic Retinopathy (DR), and Wet Age-Related Macular Degeneration (Wet-AMD). (Sourced from: https://ir.ocugen.com/news-releases/news-release-details/ocugen-presents-new-preclinical-ocu200-data-association-research)

Mechanisms of Action: VEGF Binder

Novel Mechanism: Yes

Modality: Fusion Protein

Route of Administration: Intravenous

FDA Designation: *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Ocugen
Company Location: Eastern America
Company Founding Year: 2013
Additional Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for OCU-200

Countries in Clinic: United States

Active Clinical Trial Count: 1

Recent & Upcoming Milestones

Highest Development Phases

Phase 1: Macular Edema

Trial ID

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

NCT05802329

DME

P1

Recruiting

Macular Edema

2026-07-31

50%

2025-12-04

Patient Enrollment|Primary Endpoints|Treatments