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.
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.
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?
Experts Pressure Congress to Remove Roadblocks for Biosimilars
April 12th 2025Lawmakers and expert witnesses emphasized the potential of biosimilars to lower health care costs by overcoming barriers like pharmacy benefit manager practices, limited awareness, and regulatory delays to improve access and competition in chronic disease management during a recent congressional hearing.
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.
Risk-Adjusted NPV Framework for Biosimilars Shows Key Investment Drivers
April 7th 2025Early market entry, manufacturing efficiency, and market share are critical to biosimilar development success, while technical complexity and competition heavily impact returns, according to a study presenting a risk-adjusted net present value (NPV) analysis framework.