February 03, 2026
New Danish registry data confirm the safety of switching to infliximab biosimilars, showing low rates of serious adverse events in patients with inflammatory arthritis.
February 02, 2026
January 28, 2026
January 27, 2026
January 26, 2026
November 23rd 2023
By Gillian Woollett, MA, DPhil
The legal and common uses of “interchangeability” continue to be conflated.
November 22nd 2023
By Skylar Jeremias
Several companies make moves to further their adalimumab biosimilars, Regeneron sues Celltrion over biosimilar for Eylea (aflibercept), and Health Canada grants marketing authorization for biosimilar referencing Stelara (ustekinumab).
November 21st 2023
Professionals speak to auto-substitution and its Impact on the shared decision-making process associated with biosimilars.
Medical experts discuss interchangeability designation requirements for biosimilars.
By Cameron Santoro
A China-based study where data were collected from patients with inflammatory bowel disease (IBD) showed safety and efficacy of the adalimumab biosimilar HS016.
November 20th 2023
By Sarfaraz K. Niazi, PhD
Sarfaraz K. Niazi, PhD, offers hope for the end of interchangeability labels in the United States in his latest column.
November 19th 2023
Fran Gregory, PharmD, MBA, vice president of emerging therapies at Cardinal Health, examines the evolution of the oncology biosimilar space in this special episode of Not So Different to close out Global Biosimilars Week 2023.
November 18th 2023
By Deana Ferreri, PhD
A retrospective study of New England patients receiving trastuzumab or bevacizumab found that combining dose rounding and biosimilar use resulted in greater cost savings than either strategy alone.
November 17th 2023
Here are the top 5 biosimilar articles for the week of November 13, 2023.
November 16th 2023
In partnership with The Center for Biosimilars®, the International Generic and Biosimilar Association hosted a live webinar, where panelists gathered from around the globe to discuss benefits as well as major barriers and accessibility challenges associated with oncology biosimilars worldwide.