UPTRAVI (selexipag) by Johnson & Johnson is prostacyclin receptor agonists [moa]. First approved in 2021.
Drug data last refreshed 13h ago · AI intelligence enriched 3d ago
UPTRAVI (selexipag) is a prostacyclin receptor agonist approved in 2021 for pulmonary arterial hypertension (PAH). It works by binding to prostacyclin receptors to promote vasodilation and reduce pulmonary vascular resistance. This intravenous powder formulation represents a targeted therapy for a rare, progressive cardiopulmonary disease.
UPTRAVI is in peak commercial stage with high competitive pressure (8/10), indicating an active, densely resourced brand team managing market defense and modest growth initiatives.
Prostacyclin Receptor Agonists
Prostacyclin Receptor Agonist
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Selexipag for the Treatment of Schistosomiasis-Associated Pulmonary Arterial Hypertension
A Study of Pulmonary Arterial Hypertension Participants Treated With Macitentan or Selexipag
Safety of Transition From Selexipag to Remodulin® Then Oral Treprostinil in Symptomatic Adult PAH
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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.
Johnson & Johnson is hiring 1 role related to this product
LOE in ~5 years — strategic planning for patent cliff underway
UPTRAVI offers career opportunities primarily in product management and brand commercial roles, with limited clinical development activity. The peak commercial stage with high competitive pressure indicates a brand requiring strong commercial acumen, market intelligence, and payer negotiation skills.
1 open roles linked to this drug
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