The Center for Biosimilars® recaps the top stories for the week of December 9, 2019.
Transcript
Hi, I’m Laura Joszt for The Center for Biosimilars®, your resource for clinical, regulatory, business, and policy news in the rapidly changing world of biosimilars.
Here are the top 5 biosimilars articles for the week of December 9, 2019.
Number 5: Increased spending on new oncology and autoimmune drugs was partially offset by a continued increase in the use of generics, according to a recent report from CMS.
Number 4: During this week’s 61st meeting of the American Society of Hematology, researchers reported on eculizumab, a prospective biosimilar, and a long-acting successor.
Number 3: Sanofi announced that it will stop research and development on diabetes drugs, but it will keep a proposed biosimilar of insulin aspart in its pipeline as a registration-phase molecule.
Number 2: An agreement on the United States—Mexico–Canada Agreement has been reached, and it excludes controversial terms for biologics.
Number 1: The FDA has approved Amgen’s infliximab biosimilar, Avsola, the fourth biosimilar infliximab and the 26th US biosimilar.
Finally, last week, our e-newsletter asked how great an impact you think subcutaneously administered biosimilar infliximab will have on clinical practice.
To view results of the poll, visit us on LinkedIn.
To read all of these articles and more, visit centerforbiosimilars.com.
From Amjevita to Zarxio: A Decade of US Biosimilar Approvals
March 6th 2025Since the FDA’s groundbreaking approval of Zarxio in 2015, the US biosimilars market has surged to 67 approvals across 18 originators—though the journey has been anything but smooth, with adoption facing hurdles along the way.
How AI Can Help Address Cost-Related Nonadherence to Biologic, Biosimilar Treatment
March 9th 2025Despite saving billions, biosimilars still account for only a small share of the biologics market—what's standing in the way of broader adoption and how can artificial intelligence (AI) help change that?
Will the FTC Be More PBM-Friendly Under a Second Trump Administration?
February 23rd 2025On this episode of Not So Different, we explore the Federal Trade Commission’s (FTC) second interim report on pharmacy benefit managers (PBMs) with Joe Wisniewski from Turquoise Health, discussing key issues like preferential reimbursement, drug pricing transparency, biosimilars, shifting regulations, and how a second Trump administration could reshape PBM practices.
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.