Ozmosi | Epoprostenol Drug Profile
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Epoprostenol

Alternative Names: epoprostenol, prostacyclin, prostaglandin i2, flolan, veletri
Clinical Status: Inactive
Latest Update: 2025-12-18
Latest Update Note: News Article

Product Description

Epoprostenol is a synthetic analogue of the naturally occurring eicosanoid prostacyclin (prostaglandin I2 or PGI2), which is the main metabolite of arachidonic acid (Sourced from: https://err.ersjournals.com/content/26/143/160055)

Mechanisms of Action: PGI2 Agonist, PA Inhibitor

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: Intravenous, Inhalant

FDA Designation: *

Approval Status: Approved

Approved Countries: Argentina | Australia | Austria | Belgium | Canada | Chile | Colombia | Czech | Denmark | Estonia | France | Germany | Greece | Hong Kong | Hungary | Ireland | Israel | Italy | Japan | Luxembourg | Malta | Netherlands | New Zealand | Norway | Poland | Portugal | Singapore | Slovakia | Slovenia | Spain | Sweden | Switzerland | Taiwan | Turkey | United Kingdom | United States

Approved Indications: None

Known Adverse Events: None

Company: Johnson & Johnson
Company Location: Eastern America
Company CEO: Joaquin Duato
Additional Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Epoprostenol

Countries in Clinic: United States

Active Clinical Trial Count: 1

Recent & Upcoming Milestones

Highest Development Phases

Phase 1: Hypertension, Pulmonary

Trial ID

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

NCT05427162

CR109201

P1

Completed

Hypertension, Pulmonary

2023-12-05

12%

2024-03-01

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