A Review of NeuroAiDTM II (MLC901) Development in Alzheimer’s Disease Treatment: Promises of A Multimodal Pathway

M. Dib, E. Ampil, Hoo Fan Kee, Y. Krespi, A. A. Mahdawi, S. Ogun, H. Pakdaman, K. Rejdak
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Abstract

Background: Alzheimer’s disease (AD) is a clinical and economic burden on society. Without new treatment, the impact of AD on society could triple by 2050. Aim: After a brief overview of treatments and challenges of new drug developments for AD, we reviewed the preclinical and clinical development program of NeuroAiD (MLC901, MLC601). Method: A literature search was conducted by using different web sources. The initial screening was based on keywords contained in the subtitles of each corresponding paragraphs of this article. We sorted the reviewed publications by relevance and publication date selecting 74 references out of the 319 initially shortlisted for review. Review: Since 1998, only symptomatic drugs were marketed. Intensive research has continued, aimed at delaying the onset of the disease and/or slowing its progression. However, the predictive value of delaying the onset of AD remains debated. Since 2003, aducanumab is the first new treatment approved and registered by US-FDA as an amyloid beta-directed antibody indicated for the treatment of Alzheimer’s disease under post-marketing conditions. Traditional medicines (TM) have shown interesting results, but many of TM clinical studies leave much to be desired from a methodological point of view. Among TM, NeuroAiD (MLC901/601), a botanical-derived combination, acts in a multimodal pathway combining neuroprotective and neuroregenerative properties. It has demonstrated sustained symptomatic benefits, slowing the disease progression in AD with a good safety profile. Discussion/Conclusions: The discovery of treatments preventing or slowing down the disease progression, are necessary to get reliable diagnostic tools to confirm AD diagnosis, and follow its evolution and long-term therapy. A growing consensus is emerging on the need for a multi-factorial approach to the treatment and the development of suitable AD drug combinations. Such an approach has been that of TM for a long time. This is the case for NeuroAiD, that it may be integrated safely either after symptomatic treatments have failed or on top of symptomatic treatments.
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NeuroAiDTM II (MLC901)在阿尔茨海默病治疗中的发展综述:一个多模式通路的承诺
背景:阿尔茨海默病(AD)是一个临床和社会经济负担。如果没有新的治疗方法,到2050年,阿尔茨海默病对社会的影响可能会增加两倍。目的:在简要概述AD新药开发的治疗方法和挑战后,我们回顾了NeuroAiD (MLC901, MLC601)的临床前和临床开发计划。方法:利用不同的网络资源进行文献检索。最初的筛选是基于本文每个相应段落的字幕中包含的关键词。我们根据相关性和出版日期对被评审的出版物进行了排序,从最初入围的319篇文献中选择了74篇进行评审。回顾:自1998年以来,只有对症药物上市。深入的研究仍在继续,旨在延缓疾病的发病和/或减缓其进展。然而,延迟阿尔茨海默病发病的预测价值仍然存在争议。自2003年以来,aducanumab是美国fda批准和注册的首个新疗法,作为一种淀粉样蛋白定向抗体,在上市后条件下用于治疗阿尔茨海默病。传统药物(TM)已经显示出有趣的结果,但是从方法学的角度来看,许多TM临床研究还有很多需要改进的地方。在TM中,NeuroAiD (MLC901/601)是一种植物衍生的组合药物,通过多模式途径结合神经保护和神经再生特性发挥作用。它已经证明了持续的症状益处,减缓了阿尔茨海默病的疾病进展,并具有良好的安全性。讨论/结论:发现预防或减缓疾病进展的治疗方法,获得可靠的诊断工具以确认AD的诊断,并跟踪其演变和长期治疗是必要的。越来越多的共识正在形成,需要多因素的方法来治疗和开发合适的阿尔茨海默病药物组合。长期以来,这种方法就是TM的方法。这就是NeuroAiD的情况,它可以在对症治疗失败后或在对症治疗之上安全地整合。
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