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The Top 5 Biosimilars Articles for the Week of January 20
The Center for Biosimilars® recaps the top stories for the week of January 20, 2020.
Hi, I’m Gianna Melillo 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 January 20, 2020
Number 5: Celltrion announces that it plans to launch 10 biosimilars over the next decade and will also open a large biologics manufacturing plant in China.
Number 4: A healthcare executive writes that providers should be able to help their patients reduce their out-of-pockets costs while providing the highest-quality care available through oncology biosimilars.
Number 3: Alvotech and JAMP Pharma announce a partnership to commercialize 5 biosimilars in the Canadian market.
Number 2: Gilead Science’s new chairman and chief executive officer outlines a growth plan at the J.P. Morgan Healthcare Conference.
Number 1: Teva Pharmaceuticals touts the launch of its biosimilar rituximab, Truxima, as evidence that it knows how to navigate the US pharmaceutical system.
To read all of these articles and more, visit centerforbiosimilars.com.
Real-World Data Confirm Safety of Switching Between Ranibizumab Biosimilars
March 19th 2025Patients with diabetic macular edema previously treated with a ranibizumab biosimilar in India experience comparable safety and efficacy after being switched to another ranibizumab biosimilar, demonstrating real-world safety of biosimilar-to-biosimilar switching.
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?
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.
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.
Comparable Pregnancy and Infant Milestones With Infliximab Biosimilars vs Originator in IBD
March 15th 2025A study evaluating pregnancy outcomes and infant developmental milestones found similar outcomes between pregnant women with inflammatory bowel disease (IBD) who received reference infliximab and those who received a biosimilar.
