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The Top 5 Biosimilars Articles for the Week of February 11
The Center for Biosimilars® recaps the top news for the week of February 11, 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 February 11.
Number 5: Samsung Bioepis has announced a new licensing agreement with the private equity firm C-Bridge Capital that will allow the drug maker to expand its reach into China.
Number 4: A recent Australian study found that infliximab reduces short-term costs versus colectomy in patients with acute severe ulcerative colitis, and biosimilars could drive costs down even more.
Number 3: A recent study examining Medicare Part D reimbursement policies for off-label uses found that coverage decisions could hamper patient access.
Number 2: In a long-running patent dispute, AbbVie has been ordered to produce documents related to its efforts to obtain patents to shield Humira from biosimilar competition.
Number 1: During a presentation at the Access! 2019 meeting, an IQVIA executive broke down market share data for US biosimilars.
Finally, last week, our e-newsletter asked whether you think that all biosimilars, not just interchangeable ones, should be substitutable at the pharmacy level.
To view results of the poll, visit us on LinkedIn.
To read all of these articles and more, visit centerforbiosimilars.com.
Samsung Bioepis Report Signals Turning Point for US Biosimilars
May 1st 2025A wave of biosimilar approvals, aggressive pricing strategies, and a regulatory sea change are setting the stage for unprecedented momentum in the US biologics market, with 2025 already proving to be a landmark year in reshaping cost, access, and innovation across therapeutic areas.
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.
