Results 11 to 20 of about 5,337 (191)
Aducanumab: Appropriate Use Recommendations [PDF]
Aducanumab has been approved by the US Food and Drug Administration for treatment of Alzheimer's disease (AD). Clinicians require guidance on the appropriate use of this new therapy. An Expert Panel was assembled to construct Appropriate Use Recommendations based on the participant populations, conduct of the pivotal trials of aducanumab, updated ...
Cummings, J. +5 more
core +10 more sources
Aducanumab (brand name Aduhelm) is the first FDA-approved, pharmacologic treatment for Alzheimer’s disease (AD) but many uncertainties remain regarding both efficacy and safety. Of paramount concern are associated adverse effects including cerebral edema and hemorrhage which prompted a post-approval study.
Asia Filatov, MD +1 more
openaire +3 more sources
Background Alzheimer's Disease (AD), the most common type of dementia, is a chronic, progressive, and neurodegenerative brain discomfort that causes the be damage to brain cells.
Vahit Yigit +2 more
doaj +2 more sources
Aducanumab (aducanumab-avwa; Aduhelm™) is a human, immunoglobulin gamma 1 (IgG1) monoclonal antibody directed against aggregated soluble and insoluble forms of amyloid β. It has been co-developed by Biogen and Eisai under license from Neurimmune for the treatment of Alzheimer's disease.
Sohita Dhillon (4873375)
openaire +3 more sources
Aducanumab: Appropriate Use Recommendations Update [PDF]
Aducanumab (Aduhelm) is approved in the United States for the treatment of patients with mild cognitive impairment due to Alzheimer's disease or mild AD dementia. Aducanumab Appropriate Use Recommendations (AURs) have been published and have helped guide best practices for use of aducanumab.
Cummings, Jeffrey +10 more
openaire +5 more sources
Making the Case for the Accelerated Withdrawal of Aducanumab [PDF]
U.S. Food and Drug Administration–s (FDA) approval of aducanumab (Aduhelm® in the US) as a treatment for mild cognitive impairment of the Alzheimer type and Alzheimer–s disease has raised such major concerns about efficacy, safety, FDA processes, and regulatory capture that Biogen–s license to market this biologic should be immediately withdrawn ...
Peter J, Whitehouse, Vikas, Saini
openaire +3 more sources
Making the Case for Accelerated Withdrawal of Aducanumab [PDF]
The controversial approval in June 2021 by the Food and Drug Administration (FDA) of aducanumab (marketed as Aduhelm), Biogen’s monoclonal antibody for patients with Alzheimer’s disease, raises significant concerns for the dementia field and drug approval process, considering its lack of adequate evidence for clinical efficacy, safety issues, and cost.
Whitehouse, Peter +16 more
openaire +6 more sources
Aducanumab for the treatment of Alzheimer's disease
Alzheimer's disease (AD) is the most frequent neurodegenerative condition, the most common cause of dementia, and a leading cause of disability and death globally. Mounting evidence supported accumulation of amyloid β (Aβ) as the primary cause of AD pathology and sprouted a number of candidate treatments engaging Aβ from its production to its clearance,
M. Tagliapietra, Tagliapietra, Matteo
openaire +4 more sources
Aducanumab for Alzheimer’s disease? [PDF]
Patients and families need hope, not false ...
Walsh, Sebastian +3 more
openaire +2 more sources
Aducanumab for Alzheimer’s disease: The never‐ending story that nurses should know [PDF]
In October 2019, the American pharmaceutical company Biogen stated intention to apply to the US Food and Drug Administration (FDA) for the candidate drug aducanumab to be licenced as a therapeutic agent for the treatment of Alzheimer's disease (AD).
Joel Petch +5 more
core +1 more source

