UPTRAVI (selexipag) by Johnson & Johnson is prostacyclin receptor agonists [moa]. First approved in 2021.
Drug data last refreshed 14h ago · AI intelligence enriched 1mo ago
UPTRAVI (selexipag) is a small-molecule prostacyclin receptor agonist approved in July 2021 for intravenous administration as a powder formulation. It works by selectively activating prostacyclin receptors to promote vasodilation and inhibit platelet aggregation. The drug is indicated for pulmonary arterial hypertension (PAH) patients requiring parenteral therapy.
Product is at peak commercial maturity with 4.6 years of patent protection remaining; brand teams should prepare for competitive pressures and LOE mitigation strategies.
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.
LOE in ~5 years — strategic planning for patent cliff underway
UPTRAVI offers moderate career opportunity as a peak-stage specialty pharma product within Johnson & Johnson's cardiovascular portfolio. The 4.6-year runway to LOE creates a defined career arc: early roles focus on market expansion and payer contracting, while mid-to-late tenure shifts toward LOE defense and lifecycle extension.
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