Drug data last refreshed 7h ago · AI intelligence enriched 1w ago
VARUBI (rolapitant) is an oral small-molecule NK1 receptor antagonist approved in 2015 for prevention of chemotherapy-induced nausea and vomiting (CINV). It works by blocking substance P signaling in the central nervous system, a key pathway in CINV pathophysiology. The drug is administered as a tablet prior to chemotherapy in combination with 5-HT3 antagonists and corticosteroids.
The product is in peak commercial phase with modest Part D uptake (474 claims in 2023), suggesting a niche market with limited growth trajectory and likely a smaller dedicated team.
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.
A Randomized Controlled Study of Rolapitant for the Prevention of Nausea and Vomiting Following Surgery (Study P04937AM1)(COMPLETED)
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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 ~4 years — strategic planning for patent cliff underway
VARUBI roles are concentrated in specialty commercial roles (4 linked positions), reflecting the product's niche positioning in oncology supportive care. Working on this product offers hands-on specialty account and rare disease experience, but limited upside given mature lifecycle and approaching LOE.
4 open roles linked to this drug
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