Drug data last refreshed 2h ago · AI intelligence enriched 1w ago
UDENYCA (pegfilgrastim-cbqv) is a biosimilar granulocyte colony-stimulating factor (G-CSF) approved via Biologics License Application on November 2, 2018. It is indicated to reduce the incidence of infection, as manifested by febrile neutropenia, in patients with nonmyeloid malignancies receiving myelosuppressive anti-cancer drugs. The drug works by stimulating the proliferation and differentiation of neutrophil precursor cells.
At peak lifecycle with modest Part D spending of $8M and 1,535 claims in 2023, suggesting a mature biosimilar in a competitive segment with smaller commercial footprint than reference biologic.
Leukocyte Growth Factor
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
An Analysis to Estimate Febrile Neutropenia (FN) in Patients Receiving Udenyca
UDENYCA roles are primarily commercial-facing, centered on payer negotiations, formulary placement, and market share defense in a crowded biosimilar segment. Career progression on this product emphasizes managed care expertise, contracting skills, and competitive positioning rather than clinical or development innovation.
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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.
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