Skylar Jeremias


IQVIA Report Boasts Biosimilar Uptake in Europe, Sheds Light on What’s to Come

January 10, 2023

IQVIA’s eighth edition of its Impact of Biosimilar Competition in Europe report demonstrated successful uptake in many countries throughout the region. However, not every country has great adoption rates and companies may have a harder time choosing which molecules to invest in for biosimilar development.

Dr Ivo Abraham Column: Biologics and Biosimilars—Harnessing Regulatory Data for Value, Access

January 09, 2023

Ivo Abraham, PhD, chief scientist of Matrix45 and a professor at the University of Arizona, demonstrates why regulatory bodies in the United States shouldn't look at economic evaluations when reviewing regulatory data for biosimilars in his latest column.

Study: Does Adalimumab Lose Effectiveness After Switching to a Biosimilar?

January 07, 2023

The authors of an retrospective real-world study of patients with hidradenitis suppurativa treated with adalimumab concluded that switching patients between adalimumab products risked a greater likelihood of loss of effectiveness.

FDA Accepts BLA for Alvotech Ustekinumab Biosimilar

January 06, 2023

Alvotech, an Iceland-based company, announced that the FDA accepted its biologics license application (BLA) for its proposed ustekinumab biosimilar referencing Stelara. The company said it expects the FDA’s decision in the second half of 2023.

The Top 5 Ophthalmology Articles of 2022

January 02, 2023

Biosimilar news in ophthalmology throughout the year tended to focus on the advancements of ranibizumab biosimilars, such as the US launch of Byooviz, the recall of a biobetter of ranibizumab, and the UK approval of Ongavia.

Goodbye 2022—The Top 10 Biosimilars Stories of the Year

January 01, 2023

To say goodbye to 2022 and welcome in the new year, The Center for Biosimilars recaps the biggest news stories and milestones from the past 12 months as well as list of the top 5 podcast episodes of the year.