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The Top 5 Biosimilars Articles for the Week of September 10
The Center for Biosimilars® recaps the top news for the week of September 10, 2018.
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 September 10.
Number 5: While biosimilar filgrastim and biosimilar pegfilgrastim are effective in reducing the incidence of neutropenia, adverse events were shown in a recent study to be higher in patients who receive pegfilgrastim.
Number 4: Xbrane Biopharma has announced its intention to shift its focus from generic drugs to biosimilars.
Number 3: Newly published study results show that switching to Retacrit was noninferior to continuing treatment with Epogen.
Number 2: The United Kingdom is hoping to bring more biosimilar developers’ phase 3 trials to the nation’s National Health Service.
Number 1: The FDA’s Oncologic Drugs Advisory Committee will meet next month to discuss Celltrion’s rituximab biosimilar.
Finally, last week, our e-newsletter asked whether you think that biosimilar should be approved without the need for phase 3 studies.
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
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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.
