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The Top 5 Biosimilars Articles for the Week of June 10
The Center for Biosimilars® recaps the top stories for the week of June 10, 2019.
Transcript:
Hi, I’m Samantha DiGrande 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 June 10.
Number 5: The American Medical Association has issued a call for intensified oversight of the pharmacy benefit manager industry.
Number 4: In 3 late-breaking poster presentations at the American Diabetes Association’s 79th Scientific Sessions, researchers presented data on Sanofi’s proposed insulin aspart biosimilar.
Number 3: During the European League Against Rheumatism Annual European Congress of Rheumatology, multiple research teams shared real-world evidence on biosimilar etanercept, SB4.
Number 2: A research letter in JAMA Internal Medicine raises the question of whether there is room for increased FDA transparency about regulatory filings.
Number 1: Experts weighed in on the Biosimilars Forum’s policy proposals that the group says could save the United States billions.
Finally, last week, our e-newsletter asked whether you think other payers will follow UnitedHealthcare’s lead in preferring reference pegfilgrastim over biosimilar options.
To view results of the poll, visit us on LinkedIn.
To read all of these articles and more, visit centerforbiosimilars.com.
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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?
Biosimilar Market Development Requires Strategic Flexibility and Global Partnerships
April 29th 2025Thriving in the evolving biosimilar market demands bold collaboration, early global partnerships, and a fresh approach to development strategies to overcome uncertainty and drive future success.
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.
BioRationality: EMA Accepts Waiver of Clinical Efficacy Testing of Biosimilars
April 21st 2025Sarfaraz K. Niazi, PhD, shares his latest citizen's petition to the FDA, calling on the agency to waive clinical efficacy testing in response to the European Medicines Agency's (EMA) efforts towards the same goal.
President Trump Signs Executive Order to Bring Down Drug Prices
April 16th 2025To help bring down sky-high drug prices, President Donald Trump signed an executive order pushing for faster biosimilar development, more transparency, and tougher rules on pharmacy benefit managers—aiming to save billions and make meds more affordable for everyone.
