ARANESP (darbepoetin alfa) by Amgen. Approved for erythropoiesis-stimulating agent [epc]. First approved in 2001.
Drug data last refreshed 20h ago · AI intelligence enriched 3w ago
ARANESP (darbepoetin alfa) is a long-acting erythropoiesis-stimulating agent (ESA) administered via subcutaneous injection. It is indicated for treating anemia in patients with chronic kidney disease and cancer patients receiving chemotherapy. The drug works as a cytokine that stimulates red blood cell production in the bone marrow. ARANESP represents a key therapeutic option in the ESA class, though the category faces significant safety scrutiny and competitive pressure from biosimilar alternatives.
Erythropoiesis-stimulating Agent
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Pharmacokinetic/Pharmacodynamic Parameters of NNG-DEPO (Stimus) With Aranesp® (Amgen) in Treatment of Anemia in CKD Patients on Dialysis
Canakinumab With Darbepoetin Alfa in PTs With Lower-Risk MDS Who Have Failed ESA
A Study to Compare Efficacy and Safety of Nanogen's Darbepoetin Alfa With Aranesp® (Amgen) in the Treatment of Anemia in Chronic Kidney Disease Patients on Dialysis (CKD)
A Study to Evaluate Efficacy and Safety of JTZ-951 Compared to Darbepoetin Alfa in Korean Renal Anemia Patients Receiving Hemodialysis.
The Study of PK, PD, Safety of Multiple Intravenous Injections of BCD-066 and Aranesp in Healthy Volunteers
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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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Upgrade to Pro — $25/moAmgen is hiring 1 role related to this product
ARANESP supports 1 currently open linked role, reflecting a mature product with stable staffing. Career opportunities center on brand management, renal and oncology field teams, medical science liaisons managing safety and appropriate-use messaging, and market access specialists navigating biosimilar competition. Success in this role requires deep expertise in ESA safety management, renal and oncology pathways, and biosimilar competitive strategy, as the product increasingly competes on value and outcomes rather than clinical innovation.
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