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The Top 5 Biosimilars Articles for the Week of July 24
The Center for Biosimilars recaps the top 5 stories in biosimilars news for the week of July 24, 2017.
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 July 24.
Number 5: FDA Commissioner, Dr Scott Gottlieb, along with the acting director of the Federal Trade Commission, testified before the House Judiciary Committee on Thursday concerning antitrust issues and the FDA approval process.
Number 4: A recent report on the current pipeline of biopharmaceuticals shows 749 projects under development for diabetes and diabetes-related complications.
Number 3: The House of Representatives passed the Medicare Part B Improvement Act, but the bill could face funding issues after CMS proposed a cut to payment for home healthcare.
Number 2: The prospective adalimumab biosimilar CinnoRA was shown in a recent phase 3 trial to be noninferior to Humira.
And finally, Number 1: This week, Merck announced the US launch of its biosimilar infliximab, Renflexis, at a 35% discount to Remicade.
Read these articles and more at centerforbiosimilars.com.
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.
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?
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.
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.
How State Substitution Laws Shape Insulin Biosimilar Adoption
April 15th 2025States with fewer restrictions on biosimilar substitution tend to see higher uptake of interchangeable insulin glargine, showing how even small policy details can significantly influence biosimilar adoption and expand access to more affordable insulin.
Latest Biosimilar Deals Signal Growth Across Immunology, Oncology Markets
April 14th 2025During Q1 2025, pharmaceutical companies accelerated biosimilar expansion through strategic acquisitions and partnerships in hopes of boosting patient access to lower-cost treatments in immunology and oncology.
