
Sandoz Biosimilar to Amgen's Neulasta Filed for Regulatory Approval
This is the company's third biosimilar Biologics License Application in the United States.
After a lot of skirmish, Sandoz was finally able to launch
Neulasta, a pegylated form of recombinant human granulocyte colony-stimulating factor, is indicated to reduce the incidence of infection in patients with non-myeloid malignancies who are receiving myelosuppressive anticancer agents. Neulasta was
Sandoz is a leader in generic products and has a growing biosimilar pipeline, which includes products for blockbuster molecules adalimumab (Humira) and rituximab (Rituxan). The company recently filed a BLA for a biosimilar to etanercept, a TNF-alpha inhibitor marketed as Enbrel by Amgen.
“The FDA’s acceptance of our regulatory submission for biosimilar pegfilgrastim—our third biosimilar filed in the US—demonstrates our commitment to expanding patient access to biologics in the US,” said Mark McCamish, MD, PhD, who heads Global Biopharmaceutical & Oncology Injectables Development at Sandoz.
The discussion of course could boil down to cost, once approved. Will the biosimilar cost significantly lower than its reference product, which according to patient blog posts and the website GoodRx could be priced at anywhere between $3000 and $7000 for a single injection? Neulesta is recommended to be administered once per chemotherapy cycle in adults. What would make providers switch therapy and payers consider coverage for a biosimilar that may not have a significant cost advantage?
Zarxio, the biosimilar to Neupogen,
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