New IQVIA Report: Biosimilars Driving Lower Prices and Greater Savings

Tuesday January 31, 2023

Washington, D.C. (January 31, 2023) – The Biosimilars Council released the following statement in response to the new IQVIA report, Biosimilars in the United States 2023-2027.

“Today’s IQVIA report comes at the same time as launch of the first of at least 8 lower priced biosimilar versions of Humira. Together, they highlight the opportunity to reduce patient spending through more affordable biosimilars as well as the need to address perverse market incentives under which PBMs prefer higher-priced medicines” said Craig Burton, Executive Director of the Biosimilars Council. “The report highlights the resiliency of the biosimilars market and proves once more that patient access to biosimilar medicines expands access and yields remarkable savings. To maximize savings through biosimilar adoption, policymakers should take swift action to eliminate these barriers and expand patient access to lower-priced biosimilars.”

MEDIA CONTACT:

Susan Reilly


About the Biosimilars Council

The Biosimilars Council, a division of the Association for Accessible Medicines, works to ensure a positive environment for patient access to biosimilar medicines. The Biosimilars Council is a leading source for information about the safety and efficacy of more affordable alternatives to costly brand biologic medicines. Areas of focus include public and health expert education, strategic partnerships, government affairs, legal affairs and regulatory policy. More information is available at www.biosimilarscouncil.org.

Stay Informed

Subscribe for Updates

Receive our monthly Biosimilars Bulletin and other important updates on biosimilars in the U.S.


 


Get Involved

The Council is involved in a number of events that focus on advancing biosimilars in the United States. Click on one below to learn more:

 

 

Registration Opens Soon. October 21–23, 2024 | Rockville, MD

GRx+Biosims™ 2024 is the leading regulatory science and policy event for the U.S. generics and biosimilars industry. Access the most recent information straight from experts at the Food and Drug Administration, grasp the latest policies shaping the industry, and acquire valuable insights to propel your professional development.