The Center for Biosimilars recaps the top 5 biosimilars articles for the week of February 26, 2018.
Transcript:
Hi, I’m Kelly Davio 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 February 26.
Number 5: The US Patent Trial and Appeal Board has decided that the Saint Regis Mohawk Tribe cannot claim sovereign immunity from inter partes review of Allergan’s patents covering Restasis, and that the proceedings can continue with Allergan as the patent owner.
Number 4: Infliximab has been proposed as a potential combination treatment that could enhance the effects of chemotherapy in patients with colon cancer.
Number 3: The American College of Rheumatology has updated its health policy statements for 2018, and biosimilars featured heavily in the organization’s concerns for the year ahead.
Number 2: Virginia’s House and Senate have passed a new bill that prohibits pharmacy benefit managers from penalizing pharmacists for sharing drug price information with customers.
Number 1: A health economist from Harvard Medical School is warning that, if biosimilars continue their current trajectory, they could fail to deliver on their promise to provide cost savings to the US health system.
Finally, last week, our e-newsletter asked for your thoughts on whether the extrapolation of indications for biosimilars is reasonable.
To view results of the poll, visit us on LinkedIn.
To read all of these articles and more, visit centerforbiosimilars.com.
FTC Releases Second Report on PBMs Meddling in Generic Drug Markets
January 19th 2025The 3 largest pharmacy benefit managers (PBMs) increased many specialty generic drugs prices by hundreds of percent, with some drugs seeing thousands of percent markups, according to the Federal Trade Commission (FTC)’s second interim report on PBM practices.
Biosimilars Policy Roundup for September 2024—Podcast Edition
October 6th 2024On this episode of Not So Different, we discuss the FDA's approval of a new biosimilar for treating retinal conditions, which took place in September 2024 alongside other major industry developments, including ongoing legal disputes and broader trends in market dynamics and regulatory challenges.
Eye on Pharma: Korean Drugmakers’ Impact in Europe; New Denosumab, Eculizumab Deals
January 11th 2025Korean drugmakers hold over 50% market share in the 6 best-selling biosimilar markets, 2 companies sign exclusive licensing partnership for a denosumab biosimilar, and 2 others join forces for an eculizumab biosimilar.
Senators Introduce Bipartisan Legislation to Protect Skinny Labeling
January 2nd 2025To close out the year, 4 senators came together to introduce a new bipartisan bill to protect biosimilar and generic drug manufacturers from patent litigation when obtaining “skinny label” approvals for their products.