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Abstract Details

Towards Identifying an Optimal Time for Amyloid Assessment with Donanemab Treatment
Aging, Dementia, and Behavioral Neurology
S23 - Innovations in Dementia Treatment (1:36 PM-1:48 PM)
004

Dosing with donanemab may be stopped if amyloid plaques are reduced to minimal levels based on amyloid positron emission tomography (PET) imaging. Therefore, guidance on when to assess amyloid levels for potential treatment discontinuation would be valuable to clinicians.

Elucidate the optimal timing for assessing a patient’s amyloid level in response to donanemab treatment through the use of real-world data.

The exposure-response (amyloid plaque) model (ERM, Gueorguieva et al, ADPD-2024), established based on data from three clinical trials investigating donanemab in early symptomatic Alzheimer’s disease (AD), was used to simulate amyloid reduction following the dosing regimen per the United States prescribing information. To better represent the range of baseline amyloid levels seen in clinical practice, this model included baseline amyloid PET scans collected in a real-world setting from amyloid-positive symptomatic participants (N= 3961) of the original Imaging Dementia – Evidence for Amyloid Scanning (IDEAS) study.

Assuming no dosing pauses, average amyloid reductions of 47, 63, and 68 CL were achieved at 6 months, 12 months, and 18 months, respectively. The estimated proportion of patients who reached the amyloid threshold of <24.1 CL, which is consistent with a negative amyloid PET scan by visual interpretation, was 45%, 71% and 78% after 6, 12 and 18 months of treatment, respectively. On average, more time was required to reach the post-treatment amyloid threshold for patients with higher baseline amyloid levels. In addition, the effect of various treatment disruption scenarios on amyloid reduction rate and appropriate timing for assessments will be presented.

These findings will offer insight for clinicians on when to consider conducting an amyloid PET scan to determine if a patient treated with donanemab has attained the desired amyloid reduction and can discontinue treatment.

Authors/Disclosures
Jared R. Brosch, MD (Indiana University Health)
PRESENTER
Dr. Brosch has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Eli Lilly. Dr. Brosch has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Eisai. Dr. Brosch has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Abbvie. Dr. Brosch has stock in Monument Biosciences. The institution of Dr. Brosch has received research support from Alnylam Pharmaceuticals. The institution of Dr. Brosch has received research support from Athira Pharmaceuticals. The institution of Dr. Brosch has received research support from Biogen. The institution of Dr. Brosch has received research support from EISAI. The institution of Dr. Brosch has received research support from F. Hoffman La-Roche. The institution of Dr. Brosch has received research support from University of Southern California. The institution of Dr. Brosch has received research support from Washington University. Dr. Brosch has received publishing royalties from a publication relating to health care.
Erin G. Doty, MD (Eli Lilly and Company) Dr. Doty has received personal compensation for serving as an employee of Eli Lilly and Company, USA. Dr. Doty has stock in Eli Lilly and Company, USA.
Ivelina Gueorguieva, PhD Dr. Gueorguieva has stock in Eli Lilly.
Sergey Shcherbinin, PhD Dr. Shcherbinin has received personal compensation for serving as an employee of Eli Lilly and Company. Dr. Shcherbinin has stock in Eli Lilly and Company. Dr. Shcherbinin has received intellectual property interests from a discovery or technology relating to health care.
Kay Hoong Chow Mr. Chow has received personal compensation for serving as an employee of Eli Lilly and Company. Mr. Chow has stock in Eli Lilly and Company.
Ming Lu Ming Lu has received personal compensation for serving as an employee of Eli Lilly and Company. Ming Lu has stock in Eli Lilly and Company.
John R. Sims, MD (Eli Lilly) Dr. Sims has received personal compensation for serving as an employee of Eli Lilly and Company. Dr. Sims has stock in Eli Lilly and Company.
Emily Collins (Eli Lilly) Emily Collins has received personal compensation for serving as an employee of Eli Lilly. Emily Collins has stock in Eli Lilly.
Mark A. Mintun, MD Dr. Mintun has received personal compensation for serving as an employee of Eli Lilly & Co.