Drug data last refreshed 11h ago · AI intelligence enriched 1w ago
VARUBI (rolapitant) is an oral NK1 receptor antagonist approved in 2015 for the prevention of chemotherapy-induced nausea and vomiting (CINV). It works by blocking substance P signaling in the chemoreceptor trigger zone and vomiting center. The drug is indicated for use in combination with 5-HT3 antagonists and corticosteroids in patients receiving highly emetogenic chemotherapy.
Product is in late-stage lifecycle with minimal Medicare spending and declining claim volume, suggesting reduced commercial team expansion and focus on retention activities.
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 offers limited career growth opportunities given its approaching loss of exclusivity and minimal linked job openings (4 positions). Roles center on commercial field execution and safety monitoring rather than strategic expansion or innovation.
4 open roles linked to this drug
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