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The Top 5 Biosimilars Articles for the Week of October 14, 2019
The Center for Biosimilars® recaps the top stories for the week of October 14, 2019.
Transcript
Hi, I’m Laura Joszt 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 October 14, 2019.
Number 5: A pharmacists’ group has issued a global position statement in which it recommends against treating biosimilars as interchangeable.
Number 4: A new bill would amend the Affordable Care Act to allow insulins to be approved under abbreviated new drug applications as of 2020.
Number 3: The Congressional Budget Office and CMS report that the Lower Drug Costs Now Act would save on federal spending and improve health, at least in the short term.
Number 2: In a memorandum in support of its motion to dismiss an antitrust lawsuit, AbbVie said that the complaint could upend the balance between patent and antitrust laws and hurt innovation.
Number 1: Newly introduced bipartisan legislation would require HHS to evaluate Medicare Advantage plans based on whether biosimilars are available to enrollees.
Finally, last week, our e-newsletter asked whether you think that the UK Labour party’s proposal to use compulsory licensing in order to let the government develop cheaper generics is warranted.
To view results of the poll, visit us on LinkedIn.
To read all of these articles and more, visit centerforbiosimilars.com.
Julie Reed: Why 2024 Is Important for Biosimilars
April 17th 2024Julie Reed, executive director of the Biosimilars Forum, showcases how the biosimilar industry is expected to develop throughout 2024, including major policy changes and hope for continued improvement in market share for adalimumab biosimilars.
Exploring the Biosimilar Horizon: Julie Reed's Predictions for 2024
February 18th 2024On this episode of Not So Different, Julie Reed, executive director of the Biosimilars Forum, returns to discuss her predictions for the biosimilar industry for 2024 and beyond as well as the impact that the Forum's 4 new members will have on the organization's mission.
Alvotech’s Stelara Biosimilar, Selarsdi, Receives FDA Approval
April 16th 2024Alvotech’s Selarsdi (ustekinumab-aekn), a biosimilar referencing Stelara (ustekinumab), gained FDA approval, making it the second ustekinumab biosimilar and second for the company to be given the green light for the American market.
A New Chapter: How 2023 Will Shape the US Biosimilar Space for 2024 and Beyond
December 31st 2023On this episode of Not So Different, Cencora's Brian Biehn and Corey Ford take a look back at major policy and regulatory advancements in 2023 and how these changes will alter the space going forward.
Global Biosimilar Market Projected to Reach $1.3 Trillion by 2032
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