The Center for Biosimilars® recaps the top news for the week of October 15, 2018.
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 October 15.
Number 5: During the American College of Rheumatology Annual Meeting, several research teams will present findings on nonmedical switching from reference products to biosimilars in the European Context.
Number 4: Ireland’s Medicines Management Program has opened a consultation related to its roadmap for prescribing best-value biologics in the Irish healthcare setting. The MMP will review the use of currently reimbursed anti-tumor necrosis factor therapies, which represent the highest-expenditure category for Ireland’s reimbursement plan.
Number 3: During a speech earlier this week, HHS Secretary Alex Azar proposed requiring drug companies to include the list price of a drug paid for by Medicare or Medicaid in direct-to-consumer television advertising.
Number 2: This week, UnitedHealthcare rolled out some of the changes it will be implementing in its Medicare Advantage plans beginning January 1, 2019, including listing 3 biosimilars as preferred treatments.
Number 1: Sandoz announced this week that its biosimilar adalimumab, Hyrimoz, became available in the United Kingdom, and Amgen announced that it will begin making its Amgevita available in multiple European markets. One day after the announcements from Sandoz and Amgen, Samsung Bioepis announced that it has launched its own biosimilar, Imraldi.
Finally, last week, our e-newsletter asked if Momenta’s change of direction signals trouble for the biosimilars market.
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
April 11th 2024The global biosimilar market is projected to surge from $25.1 billion in 2022 to approximately $1.3 trillion by 2032, with a compound annual growth rate of 17.6%, driven mainly by the increasing prevalence of cancer and the cost-effectiveness of biosimilars, as outlined in a report by Towards Healthcare.