Completed Brain & Nervous System Psychology & Behaviour

A systematic programme to develop and evaluate the best candidate treatments for repositioning as therapies for Alzheimer’s Disease (SMART-AD)

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A team at King’s College London will screen up to 4,000 existing drugs—already proven safe in humans—to find those that reverse the molecular signature of Alzheimer’s disease. Developing a new Alzheimer’s drug from scratch takes decades and often fails. Repositioning existing drugs cuts that timeline dramatically, because safety testing is already done. The problem is knowing which of thousands of approved drugs might work. This programme solves that by comparing the disease’s gene-activity pattern against each drug’s effect on gene expression, narrowing the field from 4,000 to 100 candidates, then to 20, then to 6, and finally to the single best candidate for a clinical trial. If successful, this could deliver a treatment ready for human trials within a few years, not decades. Even a modest delay in Alzheimer’s onset would transform millions of lives—keeping people independent longer and reducing the burden on carers and health systems. The approach also creates a reusable pipeline for other neurodegenerative diseases, turning the drug-repositioning hunt from a gamble into a systematic process.

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This innovative programme will identify drug candidates for repositioning in Alzheimer’s Disease (AD). Professor Clive Ballard and colleagues at King's College London, will compare the transcriptional signature of AD with the signatures of up to 4000 drugs with established safety in man to identify 100 candidates with the most promising therapeutic potential. State of the art gene profiling will be used to determine the ability of the candidates to modify the expression of disease-associated transcripts in hippocampal neurons, with the best 20 drugs going forward to test for biological efficacy in in-vitro assays for a wide-range of pathogenic mechanisms implicated in AD. The six agents with the most favourable impact will then be evaluated in the best rodent model of AD to obtain the proof-of-principle evidence that would support a clinical program. Importantly assays used will measure a range of key pathological and behavioural outcomes, as well as determining the drugs impact on disease-associated transcriptional changes. Each stage will be overseen by an independent expert panel to ensure drug selection is rigorous and appropriate for AD. The overall aim of this programme of research is to identify the best candidate to be taken forward to clinical trial in people with AD.

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Researchers

Clive Ballard (EPMC Awardee)

Related Research

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