AURLUMYN (iloprost) by Johnson & Johnson is 2 . First approved in 2024.
Drug data last refreshed 2h ago · AI intelligence enriched 1w ago
AURLUMYN (iloprost) is a prostacycline vasodilator and platelet aggregation inhibitor approved by the FDA in February 2024. Administered intravenously, it addresses conditions where vasodilation and anti-platelet effects are therapeutically beneficial. The drug represents a novel IV formulation of a well-characterized prostacycline mechanism.
Early commercial stage with 18+ years of patent exclusivity, suggesting sustained investment in market development and team expansion.
2 . Iloprost is a vasodilator and inhibits platelet aggregation.
Prostacycline
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Infusion of Prostacyclin (Iloprost) vs Placebo for 72-hours in Patients With Septic Shock Suffering From Organ Failure
Intravenous Iloprost in Subjects With Symptomatic Raynaud's Phenomenon Secondary to Systemic Sclerosis (Phase 3)
Intravenous Iloprost in Subjects With Symptomatic Raynaud's Phenomenon Secondary to Systemic Sclerosis (Phase 2)
Evaluation of Inhaled Iloprost Effects Using the Breelib Nebulizer, on Clinical Outcomes and Physical Activity of Patients With Advanced Pulmonary Arterial Hypertension
Examination of Ventavis (Iloprost) Inhalation Behavior Using the I-Neb AAD System in Patients With Pulmonary Arterial Hypertension When Switching the Iloprost Nebulizer Solution for Inhalation From 10 μg/mL (V10) to 20 μg/mL (V20)
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The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.
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