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Dr Hope Rugo: Talking With Other Prescribers About Biosimilars
Hope Rugo, MD, director of the breast oncology clinical trials program at the University of California at San Francisco, disucusses the conversations she is having and expects to have with fellow prescribers about biosimilars in oncology.
Transcript:
Are other breast cancer specialists looking forward to Mylan’s biosimilar trastuzumab coming to market? Are you getting questions from physicians about the biosimilar?
We haven’t really seen questions in the [United States] about biosimilars yet. I think there’s a lot of interest in understanding what a biosimilar is, [and] how the different trials have looked at biosimilars because there are many, many now out there, all looking for regulatory approval in addition to the drugs that are already approved in the [United States] and Europe.
But, I think that, because there’s a lot of experience with biosimilars in rheumatologic disease, there is a greater appreciation for the importance of biosimilars in oncology.
I think once the drugs are available, there’s going to be a big need for education and understanding of where these drugs should be and how comfortable people feel with them. But right now, I think in the United States because we can’t use them yet, that the main interest has been in supportive care and in rheumatologic disease.
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.
Eye on Pharma: EC Approved Ustekinumab; Zymfentra Expansion; Biosimilar Policy Briefing
September 26th 2024The European Commission (EC) approved Celltrion's ustekinumab biosimilar for chronic inflammatory diseases, Celltrion expanded access to Zymfentra (subcutaneous infliximab-dyyb) through partnerships with Cigna and Express Scripts, and the Association for Accessible Medicines held a policy briefing addressing barriers to biosimilar adoption.
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.
Expanding Biosimilar Adoption: Insights and Strategies With Dr Sophia Humphreys
September 16th 2024Sophia Humphreys, PharmD, MHA, BCBBS, director of system formulary management at Sutter Health, discusses the challenges of expanding biosimilars into new therapeutic areas and highlights the role of education, competitive pricing, and integrated delivery networks in improving adoption and market growth.
