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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.
Treatment Persistence, Safety After Switching to Infliximab Biosimilars in Canadians With IBD
October 5th 2024A retrospective study of a mandatory nonmedical switch in Canada found no significant differences in rates of treatment persistence, loss of response, or adverse events in patients with inflammatory bowel disease (IBD) on maintenance therapy 1 year post-switch.
Biosimilars Policy Roundup for September 2024—Podcast Edition
October 6th 2024On this episode of Not So Different, we discuss the FDA's approval of a new biosimilar for treating retinal conditions, which took place in September 2024 alongside other major industry developments, including ongoing legal disputes and broader trends in market dynamics and regulatory challenges.
Eye on Pharma: EC Approved Ustekinumab; Zymfentra Expansion; Biosimilar Policy Briefing
September 26th 2024The European Commission (EC) approved Celltrion's ustekinumab biosimilar for chronic inflammatory diseases, Celltrion expanded access to Zymfentra (subcutaneous infliximab-dyyb) through partnerships with Cigna and Express Scripts, and the Association for Accessible Medicines held a policy briefing addressing barriers to biosimilar adoption.
