Here are the top 5 biosimilar articles for the week of August 3, 2020.
Hi, I’m Skylar Jeremias 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 biosimilar articles for the week of August 3, 2020.
Number 5: The World Health Organization’s (WHO) prequalification of Celltrion Healthcare’s trastuzumab known as Herzuma, opens the door for more affordable access to care for patients with breast and gastric cancers.
Number 4: The uptake of infliximab biosimilars in the United States is slow but tracks closely to the experience in Europe, where after 2 years infliximab biosimilars assumed a large share of the market, according to a new study.
Number 3: Vizient predicts that drug price inflation, partly due to the coronavirus disease 2019 (COVID-19) pandemic, will be 3.29% in 2021 and is banking on biosimilars to help contain the rising cost of medications, it said in a comprehensive review for its member health companies.
Number 2: Amid the confusion of the pandemic, fundamental business strategies are reshaping the biosimilar playing field, according to corporate earnings reports from Alexion, Biogen, Samsung Bioepis and Frensenius Kabi
Number 1: Despite there being concerns over the safety of nonmedical switching between a reference product and a biosimilar, there is a growing body of evidence supporting the safety of switching, according to an executive of Sandoz, which produces biosimilars.
To read all of these articles and more, visit centerforbiosimilars.com.
Biosimilar Substitution Can Reduce TCOC, Improve Provider Performance in Value-Based Payment Models
December 7th 2023A simulation study estimated the impact of biosimilar substitution on total cost of care (TCOC) and provider financial performance in the final performance period of the Oncology Care Model.
Study Documents HCPs’ Experiences of a Mandatory Switch to Inform Future Transitions
December 2nd 2023A survey explores the experiences of health care providers (HCP) in New Zealand throughout the transition process following a mandatory switch from the adalimumab originator (Humira) to a biosimilar in 2022.