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Amgen Executive Discusses Prominent Biosimilar Trends
In this interview with The Center for Biosimilars®, Amgen biosimilars expert Jen Norton discusses regulatory and policy incentives, interchangeable biosimilars, and market share gains.
Amgen has multiple biosimilars in the marketplace, but also many originator drugs, which puts it on both sides of the scrimmage line.
That gives the company the perspective that policies and regulations designed to stimulate and advance biosimilar competition could be detrimental to the level of innovative investment, as it would potentially make less funding available for biopharmaceutical companies to invest in new drugs, Jen Norton, a vice president and head of US Value & Access for Amgen, says in this interview with Tony Hagen, senior editor for The Center for Biosimilars®. “Oftentimes when you create special legislation to incentivize a particular category over another category, there can be a series of downstream consequences.”
The occasion was Amgen’s presentation of findings from its 2021 Biosimilar Trends Report at the AMCP Nexus 2021 meeting this week at the Gaylord Rockies in Denver, Colorado. Norton authored the report.
Biosimilar market share gains have been strongest in the oncology space, where biosimilars emerged just in the past few years. “It’s really been impressive to see how biosimilars have taken a major role within our health care ecosystem," she says.
Some developments ahead may rival or exceed biosimilar accomplishments so far, such as the arrival of adalimumab biosimilars in 2023. Patients will be able to self-administer these, and this expansion of biosimilars into the pharmacy benefit will be a critical, market-changing event, Norton says.
Biosimilars in America: Overcoming Barriers and Maximizing Impact
July 21st 2024Join us as we explore the complexities of the US biosimilars market, discussing legislative influences, payer and provider adoption factors, and strategies to overcome industry challenges with expert insights from Kyle Noonan, PharmD, MS, value & access strategy manager at Cencora.
Stable Patient Satisfaction Found After Switching From the Humira or Biosimilar CT-P17
December 14th 2024A real-world study in France found patient satisfaction was stable after switching from either the reference product or a low-concentration adalimumab biosimilar to the adalimumab biosimilar CT-P17, a high-concentration, citrate-free formulation.
Biosimilars Oncology Roundup for June 2024—Podcast Edition
July 7th 2024On this episode of Not So Different, we review biosimilar news coming out of June, with clinical trial results from conferences and a study showcasing how to overcome economic and noneconomic barriers to oncology biosimilars.
Eye on Pharma: Golimumab Biosimilar Update; Korea Approves Denosumab; Xbrane, Intas Collaboration
December 10th 2024Alvotech and Advanz Pharma have submitted a European marketing application for their golimumab biosimilar to treat inflammatory diseases, while Celltrion secured Korean approval for denosumab biosimilars, and Intas Pharmaceuticals partnered with Xbrane Biopharma on a nivolumab biosimilar.
Pertuzumab Biosimilar Shows Promise in HER2-Positive Breast Cancer Treatment
December 9th 2024The proposed pertuzumab biosimilar QL1209 demonstrated equivalent efficacy and safety to reference pertuzumab (Perjeta) in neoadjuvant treatment of HER2-positive, ER/PR-negative early or locally advanced breast cancer, offering a cost-effective alternative with comparable clinical outcomes.
