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The Top 5 Biosimilars Articles for the Week of April 2
The Center for Biosimilars® recaps the top 5 biosimilars articles for the week of April 2, 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 April 2.
Number 5: A recently published descriptive review finds a significant time lag between the approval of biosimilar infliximab and its acceptance in Irish hospitals.
Number 4: The Senate Homeland Security and Government Affairs Committee has released a report on prescription drug price increases that affect drugs that seniors use most. According to the report, drug prices rise at approximately 10 times the rate of inflation.
Number 3: CMS will lower the maximum co-payment amount for low-income subsidy beneficiaries for biosimilars.
Number 2: Samsung Bioepis and Biogen have reached a settlement with AbbVie that will allow the biosimilar adalimumab, Imraldi, to launch in Europe later this year.
Number 1: Celltrion has announced that the FDA has issued Complete Response Letters for 2 of its proposed biosimilar products.
Also this week, expert contributor Sonia T. Oskouei explains 9 key facts about biosimilar interchangeability in the United States.
Finally, last week, our e-newsletter asked whether you think one payer’s recent decision not to undertake a nonmedical switch to a biosimilar is good news for patients.
To view results of the poll, visit us on LinkedIn.
To read all of these articles and more, visit centerforbiosimilars.com.
BioRationality: Commemorating the 15th Anniversary of the BPCIA
April 8th 2025Affirming that analytical characterization is often sufficient for biosimilar approval, minimizing unnecessary clinical testing, and enhancing FDA-led education to counter stakeholder misconceptions are key recommendations put forth in this opinion piece by Sarfaraz K. Niazi, PhD.
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.
Review Calls for Path to Global Harmonization of Biosimilar Development Regulations
March 17th 2025Global biosimilar regulatory harmonization will be needed to reduce development costs and improve patient access, despite challenges posed by differing national requirements and regulatory frameworks, according to review authors.
