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The Top 5 Biosimilars Articles for the Week of March 12
The Center for Biosimilars recaps the top 5 biosimilars articles for the week of March 12, 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 March 12.
Number 5: The European Commission has issued its eighth report on drug patent settlements, in which it found that pay-for-delay settlements in Europe have stabilized at a low level.
Number 4: A recently published study finds that biosimilar infliximab is the most cost-effective biologic treatment for fistulizing Crohn disease.
Number 3: A study investigating drivers of high spending on healthcare in the United States found that brand-name drug prices play a key role.
Number 2: Results from the VOLTAIRE-RA study showed that switching from the reference adalimumab to Boehringer Ingelheim’s FDA-approved biosimilar did not impact efficacy, safety, or immunogenicity.
Number 1: A new report predicts that 2018 will mark the beginning of a new, large wave of biosimilars.
Finally, last week, our e-newsletter asked for your thoughts on whether patient assistance programs contribute to the problem of high drug costs. To view results of the poll, visit us on LinkedIn.
To read all of these articles and more, visit centerforbiosimilars.com.
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.
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?
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.
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.
How State Substitution Laws Shape Insulin Biosimilar Adoption
April 15th 2025States with fewer restrictions on biosimilar substitution tend to see higher uptake of interchangeable insulin glargine, showing how even small policy details can significantly influence biosimilar adoption and expand access to more affordable insulin.
Latest Biosimilar Deals Signal Growth Across Immunology, Oncology Markets
April 14th 2025During Q1 2025, pharmaceutical companies accelerated biosimilar expansion through strategic acquisitions and partnerships in hopes of boosting patient access to lower-cost treatments in immunology and oncology.
