Drug data last refreshed 9h ago · AI intelligence enriched 1w ago
SAVAYSA (edoxaban tosylate) is an oral Factor Xa inhibitor anticoagulant approved in 2015 for stroke prevention and thromboembolism treatment. It is a small-molecule direct oral anticoagulant (DOAC) that works by selectively inhibiting Factor Xa, a key enzyme in the coagulation cascade. The drug is taken orally as a tablet with flexible dosing options.
With less than 2 years until loss of exclusivity and minimal Part D spending ($5M in 2023), the brand is in managed decline, requiring lean, efficiency-focused teams.
Mechanism of action data is being enriched from DailyMed and FDA sources. Check back soon for updated drug intelligence.
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Comparative Investigation of Low Molecular Weight (LMW) Heparin/Edoxaban Tosylate (DU176b) Versus (LMW) Heparin/Warfarin in the Treatment of Symptomatic Deep-Vein Blood Clots and/or Lung Blood Clots. (The Edoxaban Hokusai-VTE Study).
A Study to Assess the Safety of a Potential New Drug in Comparison to the Standard Practice of Dosing With Warfarin for Non-valvular Atrial Fibrillation
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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.
Patent cliff in ~2 years — expect lifecycle management and generic defense hiring
Working on SAVAYSA offers limited career growth; the product is in terminal decline with zero linked job openings and minimal commercial momentum. Professionals should view this as a short-term assignment focused on managing decline and protecting remaining market share, rather than a growth opportunity.
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