Author:
O’Brien John T.,Chouliaras Leonidas,Sultana Janet,Taylor John-Paul,Ballard Clive,Aarsland Dag,Blanc Frederic,Boeve Bradley,Brooks David J.,Chaudhuri K. Ray,Cummings Jeffrey,Feldman Howard H.,Flicker Leon,Galvin James E.,Grosset Donald G.,Ikeda Manabu,Kohlhaas Susan,Lawlor Brian,Lemstra Afina W.,Leroi Iracema,Londos Elisabet,Leverenz James B.,Lewis Simon,McKeith Ian,Mills Roger,Oakley Richard,Richardson Jill,Sabbagh Marwan,Skidmore John,Svennigsson Per,Tiraboschi Pietro,Weintraub Daniel,Walker Zuzana,Watson Rosie,Weil Rimona S.,Williams-Gray Caroline H.,Yarnall Alison,
Abstract
AbstractDrug repositioning and repurposing has proved useful in identifying new treatments for many diseases, which can then rapidly be brought into clinical practice. Currently, there are few effective pharmacological treatments for Lewy body dementia (which includes both dementia with Lewy bodies and Parkinson’s disease dementia) apart from cholinesterase inhibitors. We reviewed several promising compounds that might potentially be disease-modifying agents for Lewy body dementia and then undertook an International Delphi consensus study to prioritise compounds. We identified ambroxol as the top ranked agent for repurposing and identified a further six agents from the classes of tyrosine kinase inhibitors, GLP-1 receptor agonists, and angiotensin receptor blockers that were rated by the majority of our expert panel as justifying a clinical trial. It would now be timely to take forward all these compounds to Phase II or III clinical trials in Lewy body dementia.
Publisher
Springer Science and Business Media LLC
Subject
Cognitive Neuroscience,Neurology (clinical),Neurology
Cited by
7 articles.
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