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
August 21st 2023
By Sarfaraz K. Niazi, PhD
Sarfaraz K. Niazi, PhD, recapped his answers to a recent interview where he discussed his predictions on the future of the biosimilar industry in the United States.
August 20th 2023
By Skylar Jeremias
On this episode of Not So Different, Julie Reed, executive director of the Biosimilars Forum, expanded on ways to make biosimilar development faster and cheaper without compromising on safety and efficacy and how these practices can ensure a sustainable market for the future.
August 18th 2023
Here are the top 5 biosimilar articles for the week of August 14, 2023.
August 17th 2023
In Biocon’s latest quarterly earnings report, the company revealed that sales for its biosimilars portfolio rose 106% compared with the same time frame the year prior.
August 16th 2023
In STADA Arzneimittel’s first half of 2023 earnings report, the company disclosed double-digit growth, suggesting that it could see profits hit an all-time high by the end of the year.
August 15th 2023
A panel of experts discuss future opportunities with interchangeable biosimilars from payer and provider perspectives.
Experts review best practices around plan design that payers and plan sponsors should address as more interchangeable biosimilars potentially enter the market.
Jonathan Kay, MD, and Kimberly C. Chen, DO, MSHLM, discuss clinical and financial concerns related to automatic substitution at the pharmacy for an interchangeable biosimilar from a payer perspective.
By Justina Petrullo
Ranibizumab biosimilar was found to be the most cost-effective for neovascular age-related macular degeneration (nAMD), according to a recent Japanese study.
August 14th 2023
By Robert Zutaut, RPh
Robert Zutaut, RPh, a clinical specialist from McKesson Provider Solutions, quantifies the major barriers to adoption for biosimilars used to treat rheumatoid arthritis (RA) and some major considerations for health systems looking to address them.