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The Top 5 Biosimilars Articles for the Week of August 5
The Center for Biosimilars® recaps the top stories for the week of August 5, 2019.
Transcript
Hi, I’m Jaime Rosenberg 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 August 5, 2019.
Number 5: Concerns are rising that the marketplace may soon see the advent of authorized biologics, which are similar to authorized generics.
Number 4: Cancer Care Ontario is launching new educational materials as Canada awaits the arrival of additional anticancer biosimilars.
Number 3: A retrospective analysis of care delivery at Memorial Sloan Kettering Cancer Center showed that using subcutaneous rituximab resulted in substantial time savings.
Number 2: A new systematic review reported on real-world evidence on biosimilar etanercept in the treatment of inflammatory diseases.
Number 1: Momenta says that it is stopping work on its proposed adalimumab biosimilar after changes in the market related to Humira patent settlements.
Finally, last week, our e-newsletter asked whether you think that, if given the opportunity, Congress should make some changes to the existing Biologics Price Competition and Innovation Act.
To view results of the poll, visit us on LinkedIn.
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."
Samsung Bioepis Report Signals Turning Point for US Biosimilars
May 1st 2025A wave of biosimilar approvals, aggressive pricing strategies, and a regulatory sea change are setting the stage for unprecedented momentum in the US biologics market, with 2025 already proving to be a landmark year in reshaping cost, access, and innovation across therapeutic areas.
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: Sandoz Files Antitrust Suit; Yuflyma Interchangeability; Costco’s Ustekinumab Pick
April 22nd 2025Sandoz's antitrust suit against Amgen, the FDA’s interchangeability designation for Celltrion’s adalimumab biosimilar, and the inclusion of an ustekinumab biosimilar in Costco’s prescription program highlight growing momentum to expand biosimilar access and affordability for patients with chronic inflammatory diseases.
BioRationality: EMA Accepts Waiver of Clinical Efficacy Testing of Biosimilars
April 21st 2025Sarfaraz K. Niazi, PhD, shares his latest citizen's petition to the FDA, calling on the agency to waive clinical efficacy testing in response to the European Medicines Agency's (EMA) efforts towards the same goal.
