AURLUMYN (iloprost) by Johnson & Johnson is 2 . First approved in 2024.
Drug data last refreshed 14h ago · AI intelligence enriched 1w ago
AURLUMYN (iloprost) is an intravenous prostacycline analog approved by the FDA in February 2024 for vasodilation and platelet aggregation inhibition. It is delivered as an IV solution and represents a new chemical entity in the prostacycline therapeutic class. The drug is indicated for patients requiring acute hemodynamic support and antiplatelet effects.
Early-stage growth product with 17.8 years of patent protection suggests sustained commercial investment and potential team expansion over the medium term.
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)
Worked on AURLUMYN at Johnson & Johnson? Share your interview experience or compensation data (+7 days Pro)
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.
Upgrade to Pro to access patent cliff timelines and LOE dates and other premium pharma intelligence.
Upgrade to Pro — $25/moUpgrade to Pro to access CMS Part B ASP pricing data and other premium pharma intelligence.
Upgrade to Pro — $25/moAURLUMYN offers career opportunities in a newly launched, growth-stage product with strong patent protection and no direct competitors, positioning it as a priority asset for Johnson & Johnson. The elevated safety signal profile and off-label use patterns indicate high demand for experienced pharmacovigilance, medical science liaisons, and market access professionals to manage risk and define appropriate use.