FDA Approves Extended Dosing Of Amgen’s Aranesp(R) To Treat Chemotherapy-Induced Anemia

THOUSAND OAKS, Calif.--(BUSINESS WIRE)--March 27, 2006--Amgen (NASDAQ:AMGN), the world’s largest biotechnology company, today announced the U.S. Food and Drug Administration (FDA) has approved every-three-week dosing of Aranesp(R) (darbepoetin alfa) for the treatment of chemotherapy-induced anemia (low red blood cell count) in patients with non-myeloid malignancies. Aranesp is the only erythropoiesis-stimulating agent approved by the FDA for every-three-week administration.

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