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Nicholas Robert, MD: Oncologists' Comfort Level With Biosimilars
Nicholas Robert, MD, medical director of data, evidence and insights at McKesson Life Sciences, discusses how comfortable oncologists are with using biosimilars.
Transcript
So in terms of adoption, anything new faces some resistance. It depends on the impact. In conversation with my physician colleagues, supportive care is less of a hill to climb over, so to speak. When you start replacing drugs that have impact on therapeutic outcomes, physicians are cautious. I think people will be cautious. But I think the data to date certainly supports that there is certainly reason to adopt biosimilars in the therapeutic realm, so I suspect it’s going to happen. To be frank, there is an economic piece as well. If it’s a more attractive option, I think everyone is aware about the cost of healthcare, and certainly people think that biosimilars are one way to attack that problem. And I think, frankly, everyone involved is onboard to reduce healthcare costs.
Q&A With Dr Chelsee Jensen: Navigating FDA Approvals, Challenges in the Biosimilar Landscape
January 14th 2024Chelsee Jensen, PharmD, BCPS, senior pharmacy specialist and pharmaceutical formulary manager at Mayo Clinic, reacts to the biggest FDA approvals of 2023 and how she sees the adalimumab, natalizumab, and tocilizumab spaces playing out.
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.
IGBA 2023: Dr Monique Mansoura Highlights the Intersection of Geopolitical Issues, Biopharma
February 19th 2023COVID-19 allowed governments to critically examine the biopharma space to increase access to vaccines, but there's still a way to go, according to Monique Mansoura, PhD, MBA, executive director of global health security and biotechnology at the MITRE Corporation, at the International Generic and Biosimilar Medicines Association’s annual meeting.
Breaking Barriers in Osteoporosis Care: New Denosumab Biosimilars Wyost, Jubbonti Approved
June 16th 2024In this episode, The Center for Biosimilars® delves into the FDA approval of the first denosumab biosimilars, Wyost and Jubbonti (denosumab-bbdz), and discuss their potential to revolutionize osteoporosis treatment with expert insights from 2 rheumatologists.
