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.
Improving Biosimilar Access Through Global Regulatory Convergence
January 15th 2025Achieving global regulatory harmonization for biosimilar vaccines and immunotherapies is essential to improving market access, reducing costs, and enhancing patient outcomes by streamlining approval processes, fostering international collaboration, and addressing regulatory disparities.
Biosimilars in America: Overcoming Barriers and Maximizing Impact
July 21st 2024Join us as we explore the complexities of the US biosimilars market, discussing legislative influences, payer and provider adoption factors, and strategies to overcome industry challenges with expert insights from Kyle Noonan, PharmD, MS, value & access strategy manager at Cencora.
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.
Top 5 Most-Read Regulatory Articles of 2024
December 25th 2024In 2024, significant biosimilar approvals were granted by the American and European regulatory agencies, including the first interchangeability designations for biosimilars referencing ustekinumab, adalimumab, denosumab, and aflibercept, marking key regulatory milestones in improving patient access to cost-effective treatments.