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The Top 5 Biosimilars Articles for 2017
The Center for Biosimilars recaps the most-read articles of 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 most-read biosimilars articles for the year of 2017.
Number 5: In January, The Center for Biosimilars® provided a look at the marketplace for prospective biosimilars referencing Humira, Enbrel, and Remicade.
Number 4: In December, the FDA approved Mylan and Biocon’s trastuzumab biosimilar, Ogivri, referenced on Herceptin.
Number 3: In January, Pfizer announced that CMS would reimburse for its biosimilar infliximab.
Number 2: In September, the FDA released a heavily redacted Form 483, noting observations that it made when inspecting Celltrion’s manufacturing facility earlier in 2017.
Number 1: In October, the FDA issued a Complete Response Letter for Mylan and Biocon’s pegfilgrastim biosimilar, referenced on Neulasta.
To read all of these articles and more, visit centerforbiosimilars.com.
Escaping the Void: All Things Biosimilars With Craig & G
May 4th 2025To close out the Festival of Biologics, Craig Burton and Giuseppe Randazzo from the Association for Accessible Medicines and the Biosimilars Council tackle the current biosimilar landscape and how the industry can emerge from the "biosimilar void."
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?
Eye on Pharma: Interchangeability Labels and Expanded Biosimilar Partnerships
May 29th 2025The FDA designates 2 biosimilars as interchangeable, enhancing access to treatments for inflammatory diseases and multiple sclerosis, while 2 other companies expand their biosimilar partnership to include more products.
