Accelerated Approval of Aducanumab: Where Do We Stand Now?

15Citations
Citations of this article
28Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Aducanumab was approved by the Food and Drug Administration (FDA) in June 2021 to treat Alzheimer disease (AD). Its path to approval has been highly scrutinized, with many experts arguing that the FDA’s decision was premature. Accelerated approval was based on a surrogate end point, with evidence to support clinical effectiveness pending a postapproval trial by the drug company sponsor Biogen. As a result, the role of aducanumab in treating AD remains uncertain. A summary of key areas of controversy to guide informed decisions about use of this drug is provided, along with a timeline describing preapproval and postapproval events.

Cite

CITATION STYLE

APA

Barenholtz Levy, H. (2022, June 1). Accelerated Approval of Aducanumab: Where Do We Stand Now? Annals of Pharmacotherapy. SAGE Publications Inc. https://doi.org/10.1177/10600280211050405

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free