According to the Alzheimer’s Association, nearly 7 million Americans are currently living with Alzheimer's disease. By 2050, this number is projected to rise to nearly 13 million. In 2021, Alzheimer's was the fifth-leading cause of death among people aged 65 and older, making it the most common type of dementia.

A concerning statistic reveals that 60% of healthcare workers believe that the US healthcare system is not effectively supporting patients and their families in navigating dementia care, highlighting the importance of clear guidelines.

In this article, we will explore the current guidelines and consensus statements regarding Alzheimer's disease. Additionally, we will provide insight into the four most recent medications that have been approved for the treatment of Alzheimer's. Our focus will be on the guidelines and FDA updates that have recently emerged.

Part 1 - Current Alzheimer's Disease Guidelines & Consensus Statements

To start, here is a listing of the current Alzheimer's disease guidelines/consensus statements:

Part 2 - Recent FDA Approvals

Below, are the recent medications and therapies recently approved by the FDA that we anticipate being incorporated into future US guidelines:

  • LEQEMBI® (lecanemab-irmb)
    • FDA Approved on 1/27/25
    • Eisai Inc. and Biogen
    • LEQEMBI is an amyloid beta-directed antibody indicated for the treatment of Alzheimer’s disease. Treatment with LEQEMBI should be initiated in patients with mild cognitive impairment or mild dementia stage of disease, the population in which treatment was initiated in clinical trials.

  • ZUNVEYL (benzgalantamine)
    • FDA Approved on 7/29/24
    • Alpha Cognition Inc.
    • ZUNVEYL (benzgalantamine) is a cholinesterase inhibitor indicated for the treatment of mild to moderate dementia of the Alzheimer’s type in adults.

  • KISUNLA (donanemab-azbt)
    • FDA Approved on 7/2/24
    • Eli Lilly and Company
    • KISUNLA is an amyloid beta-directed antibody indicated for the treatment of Alzheimer's disease. Treatment with KISUNLA should be initiated in patients with mild cognitive impairment or mild dementia stage of disease, the population in which treatment was initiated in the clinical trials.

  • REXULTI® (brexpiprazole)
    • FDA Approved on 5/11/23
    • Otsuka America Pharmaceutical, Inc. and Lundbeck
    • REXULTI is an atypical antipsychotic indicated for treatment of agitation associated with dementia due to Alzheimer’s disease.

Thank you for taking the time to review the current Alzheimer's disease guidelines/consensus, as well as the recent major changes and FDA approvals that have recently occurred. We value your feedback and would like to hear your suggestions for future topics to be covered in our guideline series. Please feel free to contact us with any ideas or questions you may have.

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