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Dr Vibeke Strand: The Current State of Immunology Biosimilars and the Promise of Future Savings
In light of 2 blockbuster originators, namely Humira (adalimumab) and Stelara (ustekinumab), losing market exclusivity in 2023, 3 doctors penned supplement in The American Journal of Managed Care®. On this episode, Vibeke Strand, MD, one of the co-authors, explored how health systems can take charge and boost biosimilar adoption.
It's no secret that the immunology space for biosimilars is growing and growing fast, with between 8 and 10 adalimumab biosimilars and at least 2 ustekinumab biosimilars expected to launch in the United States throughout 2023. In light of 2 of the most profitable originators, namely Humira (adalimumab) and Stelara (ustekinumab), losing market exclusivity around the same time, 3 doctors in the immunology space penned a 3-article supplement in The American Journal of Managed Care® entitled "Biosimilars for Immune-Mediated Inflammatory Diseases: 2022 Update."
The Center for Biosimilars®, the sister website of The American Journal of Managed Care®, is conducting a multimedia interview series with the authors to expand on some of the information presented in the supplement. On this episode of Not So Different, we spoke with Vibeke Strand, MD, one of the co-authors and an adjunct clinical professor in the Division of Immunology/Rheumatology at Stanford University School of Medicine. We discussed the article "Overview of Biosimilars for Immune-Mediated Inflammatory Diseases: Summary of Current Evidence" as well as how health systems can take charge and try to boost biosimilar adoption.
Show notes
To read all the articles within the supplement, click here.
To read the article references in this episode, click here.
Disease Activity, Safety Remain Following Switch From Infliximab Biosimilar to Remicade in IBD
February 15th 2025Switching back from infliximab biosimilar SB2 to reference infliximab (Remicade) did not affect clinical disease activity or safety in inflammatory bowel disease (IBD), according to a prospective cohort study.
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.
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.
The Biosimilar Void: 90% of Biologics Coming Off Patent Will Lack Biosimilars
February 5th 2025Of the 118 biologics losing exclusivity over the next decade, only 10% have biosimilars in development, meaning a vast majority of biologics have no pipeline, which limits savings potential for the health care system.
The Banking of Biosimilars: Insights From a Leading Health Economist
February 4th 2025Biosimilars have the potential to reduce health care costs and expand patient access, but economic and policy barriers affect adoption, explored James D. Chambers, PhD, MPharm, MSc, associate professor at the Tufts Medical Center Institute for Clinical Research and Health Policy Studies, in an interview.
