UPTRAVI (selexipag) by Johnson & Johnson is prostacyclin receptor agonists [moa]. First approved in 2015.
Drug data last refreshed 8h ago · AI intelligence enriched 3d ago
UPTRAVI (selexipag) is an oral prostacyclin receptor agonist approved in 2015 for pulmonary arterial hypertension (PAH). It works by mimicking prostacyclin, a naturally occurring vasodilator that reduces pulmonary vascular resistance and improves exercise capacity in PAH patients. This is the only selective prostacyclin receptor (IP) agonist available in oral form.
UPTRAVI is in peak lifecycle stage with substantial Medicare spending, indicating a mature, stable commercial franchise with established market presence and stable team sizing.
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
$758M Medicare spend — this is a commercially significant brand
UPTRAVI supports 1,407+ linked job opportunities across J&J's portfolio, with strongest demand in Commercial, Quality Assurance, and R&D functions. Working on this product means joining a stable, mature franchise with focus on market maintenance, compliance, and operational excellence rather than launch dynamics.
1407 open roles linked to this drug
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