The Center for Biosimilars® recaps the top stories for the week of June 17, 2019.
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 June 17.
Number 5: During the 24th Congress of the European Hematology Association, researchers reported on findings from a phase 1 trial of Amgen’s proposed eculizumab biosimilar.
Number 4: At the European League Against Rheumatism’s Annual European Congress of Rheumatology, researchers said a biosimilar adalimumab has a “significant advantage” over the reference in terms of injection pain.
Number 3: Irish hospitals will be offered an incentive for each patient switched from brand-name Humira or Enbrel to a biosimilar option.
Number 2: A new study has found that switching among multiple biosimilar infliximab products was not associated with increased immunogenicity.
Number 1: A Canadian advisory council is recommending the use of biosimilars in a final report that lays out recommendations for how the country can create a single-payer public system for pharmaceutical coverage.
Finally, last week, our e-newsletter asked whether you think that anticancer biosimilars will have swifter US uptake than biosimilars that treat inflammatory diseases.
To view results of the poll, visit us on LinkedIn.
To read all of these articles and more, visit centerforbiosimilars.com.
Competitive Pricing in Biosimilars: How Adalimumab Could Shape the Industry
Published: October 29th 2024 | Updated: October 29th 2024Sophia Humphreys, PharmD, MHA, BCBBS, of Sutter Health notes that although initial adoption of adalimumab biosimilars remained low in 2023, competitive pricing pressures have already benefited patients and the health care sector.
Biosimilars Policy Roundup for September 2024—Podcast Edition
October 6th 2024On this episode of Not So Different, we discuss the FDA's approval of a new biosimilar for treating retinal conditions, which took place in September 2024 alongside other major industry developments, including ongoing legal disputes and broader trends in market dynamics and regulatory challenges.
FDA and Industry Experts Unpack Biosimilar Device Requirements
October 23rd 2024At the GRx+Biosims 2024 conference, a panel of industry experts and FDA officials discussed evolving device requirements for biosimilars and interchangeable biosimilars, highlighting new approaches to comparative use human factors studies, regulatory challenges, and alternative validation methods.
Calling for Unified Biosimilar Standards, Stronger Education at GRx+Biosims
October 23rd 2024At the GRx+Biosims conference, a fireside chat highlighted the need to streamline biosimilar development and strengthen industry collaboration, with Sarah Yim, MD, of the FDA, emphasizing education's key role in building trust and adoption.