A randomized, double‐blind, placebo‐controlled, multiple ascending dose study to evaluate the efficacy, pharmacokinetics, and safety of ABBV‐916 in adults with early Alzheimer’s disease

Preliminary data suggest that the safety and PK profile of ABBV-916 is comparable to currently approved anti-amyloid immunotherapies for the treatment of AD. Brain amyloid reduction was observed at doses of 300 mg or higher.

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Publication Details

Journal
Alzheimer s & Dementia
Published
2025-12-01
DOI
https://doi.org/10.1002/alz70859_102775
Primary Topic
Alzheimer's disease research and treatments
Type
article
Field-Weighted Citation Impact
0.00
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article

A randomized, double‐blind, placebo‐controlled, multiple ascending dose study to evaluate the efficacy, pharmacokinetics, and safety of ABBV‐916 in adults with early Alzheimer’s disease

D. Wang, Hao Xiong, Hana Florian, Anthony W. Bannon et al.
Alzheimer s & Dementia
Alzheimer's disease research and treatments
article

A randomized, double‐blind, placebo‐controlled, multiple ascending dose study to evaluate the efficacy, pharmacokinetics, and safety of ABBV‐916 in adults with early Alzheimer’s disease

D. Wang, Hao Xiong, Hana Florian, Anthony W. Bannon, Ole Graff, Joey Boiser, Edwin Stage, Shau Yu Lynch, Yamin Wang, Sagar Bachhav
article en

Abstract

Preliminary data suggest that the safety and PK profile of ABBV-916 is comparable to currently approved anti-amyloid immunotherapies for the treatment of AD. Brain amyloid reduction was observed at doses of 300 mg or higher.

Alzheimer s & DementiaVol. 21(S5)
AbbVie (United States) (US)
Good health and well-being
Openalex Percentile: Top 33%
Alzheimer's disease research and treatments
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