Brief of over 300 reproductive health researchers as Amici Curiae in FDA v. Alliance for Hippocratic Medicine

Author:

Barrow Amanda1,Cohen Cathren1,Serpico Jaclyn1,Goodman Melissa1,Grossman Daniel2,Raifman Sarah2,Upadhyay Ushma2

Affiliation:

1. University of California Los Angeles Center on Reproductive Health, Law, and Policy Los Angeles California USA

2. Advancing New Standards in Reproductive Health, Department of Obstetrics, Gynecology, & Reproductive Sciences University of California San Francisco Oakland California USA

Abstract

AbstractOn January 30, 2024, over 300 researchers filed an amicus brief in FDA v. Alliance for Hippocratic Medicine, a United States (US) Supreme Court case that could have severely impacted access to mifepristone, one of the two drugs commonly used in medication abortion. The researchers summarize the legal challenges to the US Food and Drug Administration's (FDA's) original approval of mifepristone in 2000 and its 2016 and 2021 decisions modifying mifepristone's Risk Evaluation and Mitigation Strategy (REMS) Program and label, the responses from the FDA and drug manufacturer to the challenges, and the potential implications of the Court's decision on access to mifepristone in the US. The researchers detail how the FDA relied on a robust scientific record analyzing tens of thousands of patient experiences that conclusively demonstrated the safety and effectiveness of the changes to the mifepristone REMS Program and label and urge the Supreme Court to rely on the clear scientific record and preserve access to mifepristone without reimposing restrictions. What follows is a reprint of this brief.

Publisher

Wiley

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