REMTERNETUG: AN INVESTIGATIONAL MONOCLONAL ANTIBODY AGAINST Β-AMYLOID FOR THE TREATMENT OF ALZHEIMER’S DISEASE (AD)

Authors

  • MANMEET KAUR Department of Pharmacology, Kalpana Chawla Government Medical College, Karnal, India
  • SAURAV MISRA Department of Pharmacology, Kalpana Chawla Government Medical College, Karnal, India

DOI:

https://doi.org/10.22159/ijcpr.2025v17i3.55038

Keywords:

Alzheimer’s disease (AD), Monoclonal antibody, Remternetug, β-amyloid, Drug development, Evidences

Abstract

In today's aging world, Alzheimer’s disease (AD) is a leading cause of dementia and a major chronic illness among the elderly, affecting 55 million people. The World Health Organization (WHO) has identified AD as a top public health priority. Unfortunately, there are currently no definitive cures for this condition. Treatment strategies primarily focus on alleviating symptoms, such as acetylcholinesterase inhibitors (AChEI) and the N-Methyl-D-aspartate (NMDA) antagonist Memantine. The most effective approaches for managing the disease at present appear to involve a combination of medication and non-medication-based therapies aimed at stimulating cognitive reserve. Over the past two decades, several drugs have been discovered that target the established biological indicators of AD, including the build-up of β-amyloid aggregates and the accumulation of hyperphosphorylated tau protein within cells. The amyloid cascade hypothesis is a useful framework for developing therapies for Alzheimer’s disease (AD). Experimental treatments have targeted amyloid b1-42 (Aβ) due to its neurotoxic effects and potential adverse effects on the brain, detectable through positron emission tomography (PET). Recent trials support the clinical efficacy of third-generation anti-amyloid immunotherapies in reducing brain Aβ burden and preventing cognitive decline. This has led to the recent FDA approval of aducanumab and lecanemab under an accelerated approval pathway. In this overview, we aimed to assess the safety and effectiveness of Remternetug in treating AD. Remternetug is an enhanced version of donanemab that also targets N-terminal pyroglutamated Aβ. The initial findings show promise for the development of an effective novel drug. However, more phase III studies are needed to provide sufficient clinical evidence for its effectiveness. Current evidence is limited to phase I and II studies and has yet to prove its worth in a larger population.

Downloads

Download data is not yet available.

References

Shukla AK, Misra S. Evidences and therapeutic advantages of donanemab in the treatment of early alzheimers disease. J Basic Clin Physiol Pharmacol. 2024;35(1-2):25-9. doi: 10.1515/jbcpp-2023-0176, PMID 38053285.

Kumar A, Sidhu J, Lui F, Tsao JW. Alzheimer Disease. In: StatPearls. In: Treasure Island, (FL): StatPearls Publishing; 2024 Jan. Available from: https://www.ncbi.nlm.nih[Gov/books/NBK499922].

Ahmad FB, Cisewski JA, XU J, Anderson RN. Provisional mortality data United States; 2022. MMWR Morb Mortal Wkly Rep. 2023;72(18):488-92. doi: 10.15585/mmwr.mm7218a3, PMID 37141156.

National Institute on Aging. Alzheimers Dis Fact Sheet. Available from: https://www.nia.nih.gov/health/alzheimers-and-dementia/alzheimers-disease-fact-sheet. [Last accessed on 01 Oct 2024].

Breijyeh Z, Karaman R. Comprehensive review on alzheimers disease: causes and treatment. Molecules. 2020;25(24):5789. doi: 10.3390/molecules25245789, PMID 33302541.

Singh R, Stat Pearls SNM. Pearls publishing; Treasure Island, FL, USA. Stat; 2020. Cholinesterase Inhibitors. Available from: https://www.ncbi.nlm.nih.gov/books/NBK544336. [Last accessed on 17 Oct 2024].

Eldufani J, Blaise G. The role of acetylcholinesterase inhibitors such as neostigmine and rivastigmine on chronic pain and cognitive function in aging: a review of recent clinical applications. Alzheimers Dement (NY). 2019;5:175-83. doi: 10.1016/j.trci.2019.03.004, PMID 31194017.

Sharma K. Cholinesterase inhibitors as Alzheimer therapeutics. Mol Med Rep. 2019;20(2):1479-87. doi: 10.3892/mmr.2019.10374, PMID 31257471.

Briggs R, Kennelly SP, O Neill D. Drug treatments in alzheimers disease. Clinical Medicine. 2016;16(3):247-53. doi: 10.7861/clinmedicine.16-3-247.

Mendez MF. Early onset alzheimer disease. Neurol Clin. 2017 May;35(2):263-81. doi: 10.1016/j.ncl.2017.01.005, PMID 28410659.

An Armstrong RA. Risk factors for alzheimers disease. Folia Neuropathol. 2019;57(2):87-105. doi: 10.5114/fn.2019.85929, PMID 31556570.

Serrano Pozo A, Frosch MP, Masliah E, Hyman BT. Neuropathological alterations in alzheimer disease. Cold Spring Harb Perspect Med. 2011;1(1):a006189. doi: 10.1101/cshperspect.a006189, PMID 22229116.

Spires-Jones TL, Hyman BT. The intersection of amyloid beta and tau at synapses in alzheimers disease. Neuron. 2014;82(4):756-71. doi: 10.1016/j.neuron.2014.05.004, PMID 24853936.

Singh SK, Srivastav S, Yadav AK, Srikrishna S, Perry G. Overview of alzheimers disease and some therapeutic approaches targeting abeta by using several synthetic and herbal compounds. Oxid Med Cell Longev. 2016;2016:7361613. doi: 10.1155/2016/7361613, PMID 27034741.

Alzforum. Remternetug. Available from: https://www.alzforum.org/therapeutics/remternetug. [Last accessed on 01 Oct 2024].

Neatu M, Covaliu A, Ionita I, Jugurt A, Davidescu EI, Popescu BO. Monoclonal antibody therapy in alzheimers disease. Pharmaceutics. 2023 Dec 29;16(1):60. doi: 10.3390/pharmaceutics16010060, PMID 38258071.

Alzforum. Next goals for immunotherapy: make it safer less of a hassle. International conference on alzheimers and parkinsons diseases; 2023. Available from: https://www.alzforum.org/news/conference-coverage/next-goals-immunotherapy-make-it-safer-less-hassle.

Clinical Trial. A study of ly3372993. In: participants with alzheimers disease (ad) and healthy participantsnct04451408. Available from: https://clinicaltrials.gov/study/NCT04451408?term=NCT04451408andrank=1. [Last accessed on 17 Oct 2024].

Clinical Trial. A study of remternetug (ly3372993) in participants with alzheimers disease (Trailrunner-alz1) nct05463731. Available from: https://clinicaltrials.gov/study/nct05463731?term=nct05463731andrank=1. [Last accessed on 17 Oct 2024].

Cummings J, Osse AM, Cammann D, Powell J, Chen J. Anti-amyloid monoclonal antibodies for the treatment of alzheimers disease. Bio Drugs. 2024 Jan;38(1):5-22. doi: 10.1007/s40259-023-00633-2, PMID 37955845.

Cummings J. Anti-amyloid monoclonal antibodies are transformative treatments that redefine alzheimers disease therapeutics. Drugs. 2023;83(7):569-76. doi: 10.1007/s40265-023-01858-9, PMID 37060386.

Published

15-05-2025

How to Cite

KAUR, MANMEET, and SAURAV MISRA. “REMTERNETUG: AN INVESTIGATIONAL MONOCLONAL ANTIBODY AGAINST Β-AMYLOID FOR THE TREATMENT OF ALZHEIMER’S DISEASE (AD)”. International Journal of Current Pharmaceutical Research, vol. 17, no. 3, May 2025, pp. 7-9, doi:10.22159/ijcpr.2025v17i3.55038.

Issue

Section

Review Article(s)