Cited by 7Alzheimer's disease research and treatmentsCholinesterase and Neurodegenerative DiseasesIntellectual Property and Patents

Pharmacological Inventions for Alzheimer Treatment in the United States of America: A Revision Patent from 2010–2020

Open access
Navarro-Gómez, N., Valdes-Gonzalez, M., Garrido-Suárez, B.B., Garrido, Gabino·2023·The Journal of Prevention of Alzheimer's Disease

Abstract

Alzheimer's disease (AD) is the most common form of dementia. There is currently no cure, and the available pharmacological treatment focuses on treating the symptoms. This study aimed to analyze the pharmacological treatments for AD protected in the US Patent Office. The Matheo Patent software was used to search for patents granted in the 2010-2020 period in the USPTO database. The search strategy «Alzheimer» was used in title and abstract and the International Patent Classification (IPC) codes A61P* and A61K*. The selected patents were divided into six categories according to therapeutic target. Complementary information from scientific databases was used to determine the stage of investigation and efficacy of the patented molecules. In the analyzed period, 58 patents were granted: 10 directed to Aβ peptide metabolism and deposition, three to tau, seven to inflammation, nine to cholinergic, two to glutamatergic and 27 to other targets. More than 80.0% belong to holders from the USA, France, and Japan. The molecules Elenbecestat and LY3202626 decreased the burden of Aβ plaques without significant cognitive improvement, Donanemab is in Phase 3 clinical trial, and the FDA has designated it Breakthrough Therapy. CPC-201 and PXT864 demonstrated, in Phase 2, good tolerability and improvement of AD symptoms. Most of the inventions are focused on treating the earliest phase of AD. The most advanced treatments in their research are those focused on treating Aβ accumulation. More stu…

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Crossref · 10.14283/jpad.2023.2

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  • A phase III trial of elenbecestat in early-stage AD patients was terminated due to an unfavorable risk-benefit ratio, specifically lack of help in cognition and side effects such as nightmares, weight loss, rash, and liver damage.

    “A phase III trial (NCT02956486) assessing effectiveness and safety in early-stage AD patients was terminated due to an unfavorable risk-benefit ratio. More specifically, literature446,449 indicates that the termination was due to the lack of help in cognition and the emergence of side effects such as nightmares, weight loss, rash, and liver damage.”

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References 66 · Cited by 7

Authors
Navarro-Gómez, N., Valdes-Gonzalez, M., Garrido-Suárez, B. B., & Garrido, G.
Affiliations
  • Universidad Católica del Norte (CL)
  • University of Havana (CU)
Corresponding author
Garrido, Gabino
Venue
The Journal of Prevention of Alzheimer's Disease
Publisher
Elsevier BV
Published
2023-01
Volume
10
Issue
1
Pages
50-68
ISSN
2274-5807 (ISSN-L)
OpenAlex
W4313476161
Cited by
7
References
66
Citations by year
2026: 1 · 2025: 3 · 2024: 2 · 2023: 1
FWCI
1.24
Type
journal article
Language
en
Open access
Locations
  • The Journal of Prevention of Alzheimer s Disease (publishedVersion, cc-by-nc-nd)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
  • Health Sciences › Medicine › Pharmacology › Cholinesterase and Neurodegenerative Diseases
  • Social Sciences › Business, Management and Accounting › Management of Technology and Innovation › Intellectual Property and Patents
Keywords
Alzheimer's disease, pharmaceutical patents, amyloid-beta, tau protein, neuroinflammation, cholinergic drugs, glutamatergic drugs, donanemab, breakthrough therapy designation, drug development
MeSH terms
Alzheimer Disease, France, Humans, Japan, Patents as Topic, United States

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