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The Top 5 Biosimilars Articles for the Week of June 3
The Center for Biosimilars® recaps the top stories for the week of June 3, 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 June 3.
Number 5: Prestige BioPharma announced that the European Medicines Agency will review its application for a proposed trastuzumab biosimilar, HD201.
Number 4: During this week’s 2019 American Society of Clinical Oncology Annual Meeting (ASCO), researchers presented the final overall survival results from the phase 3 HERITAGE study of biosimilar trastuzumab, Ogivri.
Number 3: Also at ASCO, Samsung Bioepis presented long-awaited 3-year results for its biosimilar trastuzumab, Ontruzant.
Number 2: With patents on reference products that treat multiple sclerosis set to expire soon in Latin America, a panel of experts published a set of recommendations on biosimilars in the region.
Number 1: Ahead of the anticipated 2019 marketing of FDA-approved anticancer biosimilars in the United States, a pharmacy benefit manager is launching an oncology biosimilar program.
Finally, last week, our e-newsletter asked whether you think other states will follow Colorado’s lead in capping patients’ costs for insulin.
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.
BioRationality: Removing the Misconceptions Surrounding Interchangeability
April 15th 2024Sarfaraz K. Niazi, PhD, outlines the current state of interchangeable biosimilars in the US and policy changes needed to clear up misconceptions surrounding the meaning behind interchangeability designations.
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.
