Illinois Cognitive Resources Network

Connecting to resources throughout your dementia journey

Subscribe to ICRN E-News blasts

FDA Hears Crushing Impact of Alzheimer’s

President and CEO Update: Alzheimer’s Association

This message is sent to all Alzheimer’s Association and Alzheimer’s Impact Movement board members, all Alzheimer’s Association staff, and volunteers and supporters of AIM and the Alzheimer’s Association.

Last week, the Food and Drug Administration (FDA) heard the heart-wrenching personal stories of individuals whose lives have been devastated by Alzheimer’s disease.

The Alzheimer’s Association worked directly with the FDA to arrange this session as part of our advocacy for new treatments. We were deeply concerned that the voices of those diagnosed with Alzheimer’s and their caregivers had not truly been heard during a recent advisory committee meeting on aducanumab, an Alzheimer’s treatment developed by Biogen, now under review by the FDA.

On behalf of the millions of Americans facing Alzheimer’s every day, the speakers candidly and powerfully used their voices to communicate the immediate need for treatment to FDA leaders. We are deeply grateful to each of the speakers, who so openly, and often emotionally, talked about the crushing impact of Alzheimer’s on their own lives and the lives of their loved ones.

Hearing the staggering realities of living with Alzheimer’s, with no treatment available for its underlying cause, the FDA participants were certainly engaged and expressed their appreciation for the speakers’ openness and honesty.

I told the FDA leaders that the Alzheimer’s Association, as a science-driven organization, continues to believe what we have told them previously, that aducanamab should be approved.

If approved, it would be the first treatment to potentially change the progression of Alzheimer’s, not just the symptoms. We believe the accumulated science, the publicly released data on aducanumab and the absence of any other treatment addressing the cause of the disease justifies FDA approval, accompanied by a Phase 4 post marketing surveillance study.

Be assured, we will keep working on this on behalf of the millions affected by Alzheimer’s until a decision is made. And then, whatever the decision, we’ll continue to work relentlessly until we realize our vision of a world without Alzheimer’s.

I will share more news with you when the FDA makes its final decision. As always, thank you for everything you do to advance our mission to make a difference for others — today and tomorrow.

Harry Johns
Chief Executive Officer

Last Updated on January 25, 2021

Published by Chrishun Brown

Communications Manager for the Rush Alzheimer's Disease Center

Leave a Reply

This site uses Akismet to reduce spam. Learn how your comment data is processed.