Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2011 Oct 22;71(15):2031-65.
doi: 10.2165/11595870-000000000-00000.

Current and emerging drug treatment options for Alzheimer's disease: a systematic review

Affiliations

Current and emerging drug treatment options for Alzheimer's disease: a systematic review

Nathan Herrmann et al. Drugs. .

Abstract

Alzheimer's disease (AD) is a progressive and ultimately fatal condition that causes debilitating memory loss and extensive deterioration of cognitive and functional abilities. Currently available treatments for AD (donepezil, rivastigmine, galantamine and memantine) are symptomatic and do not decelerate or prevent the progression of the disease. These therapies demonstrate modest, but particularly consistent, benefit for cognition, global status and functional ability. The search for disease-modifying interventions has focused largely on compounds targeting the amyloid-β pathway. To date, the treatments targeting this pathway, such as tramiprosate and semagacestat, have been unsuccessful in demonstrating efficacy in clinical stages of testing. At this point, it is likely that not only amyloid-β aggregation but other possible neuronal mechanisms - such as hyperphosphorylated tau, neuro-inflammation and other processes - play important roles in the pathophysiology of this multifactorial disorder. Development of better disease models and biomarkers is essential for the advancement of knowledge of the disease mechanisms. This systematic review critically examines the efficacy and safety data for currently approved drugs and emerging treatments in AD, as well as discussing the present and future directions of innovation in this field.

PubMed Disclaimer

References

    1. JAMA. 1994 Apr 6;271(13):992-8 - PubMed
    1. Neurology. 2005 May 10;64(9):1553-62 - PubMed
    1. Brain. 2006 Nov;129(Pt 11):3035-41 - PubMed
    1. Cochrane Database Syst Rev. 2006 Jan 25;(1):CD001747 - PubMed
    1. Curr Opin Investig Drugs. 2009 Jul;10(7):721-30 - PubMed

Publication types

MeSH terms

LinkOut - more resources