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Alzheimer's disease drug development pipeline: 2019

INTRODUCTION: Alzheimer's disease (AD) has few available treatments, and there is a high rate of failure in AD drug development programs. Study of the AD drug development pipeline can provide insight into the evolution of drug development and how best to optimize development practices. METHODS:...

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Autores principales: Cummings, Jeffrey, Lee, Garam, Ritter, Aaron, Sabbagh, Marwan, Zhong, Kate
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6617248/
https://www.ncbi.nlm.nih.gov/pubmed/31334330
http://dx.doi.org/10.1016/j.trci.2019.05.008
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author Cummings, Jeffrey
Lee, Garam
Ritter, Aaron
Sabbagh, Marwan
Zhong, Kate
author_facet Cummings, Jeffrey
Lee, Garam
Ritter, Aaron
Sabbagh, Marwan
Zhong, Kate
author_sort Cummings, Jeffrey
collection PubMed
description INTRODUCTION: Alzheimer's disease (AD) has few available treatments, and there is a high rate of failure in AD drug development programs. Study of the AD drug development pipeline can provide insight into the evolution of drug development and how best to optimize development practices. METHODS: We reviewed clinicaltrials.gov and identified all pharmacologic AD trials of all agents currently being developed for treatment of AD. RESULTS: There are 132 agents in clinical trials for the treatment of AD. Twenty-eight agents are in 42 phase 3 trials; 74 agents are in 83 phase 2 trials; and 30 agents are in 31 phase 1 trials. There is an increase in the number of agents in each phase compared with that in the 2018 pipeline. Nineteen agents in trials target cognitive enhancement, and 14 are intended to treat neuropsychiatric and behavioral symptoms. There are 96 agents in disease modification trials; of these, 38 (40%) have amyloid as the primary target or as one of several effects. Eighteen of the antiamyloid agents are small molecules, and 20 are monoclonal antibodies or biological therapies. Seven small molecules and ten biologics have tau as a primary or combination target (18%). Amyloid is the most common specific target in phase 3 and phase 2 disease modification trials. Novel biomarkers (e.g., neurofilament light), new outcomes (e.g., AD Composite Score [ADCOMS]), enrollment of earlier populations, and innovative trial designs (e.g., Bayesian adaptive designs) are new features in recent clinical trials. DISCUSSION: Drug development continues robustly at all phases despite setbacks in several programs in the recent past. Continuing unmet needs require a commitment to growing and accelerating the pipeline.
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spelling pubmed-66172482019-07-22 Alzheimer's disease drug development pipeline: 2019 Cummings, Jeffrey Lee, Garam Ritter, Aaron Sabbagh, Marwan Zhong, Kate Alzheimers Dement (N Y) Featured Article INTRODUCTION: Alzheimer's disease (AD) has few available treatments, and there is a high rate of failure in AD drug development programs. Study of the AD drug development pipeline can provide insight into the evolution of drug development and how best to optimize development practices. METHODS: We reviewed clinicaltrials.gov and identified all pharmacologic AD trials of all agents currently being developed for treatment of AD. RESULTS: There are 132 agents in clinical trials for the treatment of AD. Twenty-eight agents are in 42 phase 3 trials; 74 agents are in 83 phase 2 trials; and 30 agents are in 31 phase 1 trials. There is an increase in the number of agents in each phase compared with that in the 2018 pipeline. Nineteen agents in trials target cognitive enhancement, and 14 are intended to treat neuropsychiatric and behavioral symptoms. There are 96 agents in disease modification trials; of these, 38 (40%) have amyloid as the primary target or as one of several effects. Eighteen of the antiamyloid agents are small molecules, and 20 are monoclonal antibodies or biological therapies. Seven small molecules and ten biologics have tau as a primary or combination target (18%). Amyloid is the most common specific target in phase 3 and phase 2 disease modification trials. Novel biomarkers (e.g., neurofilament light), new outcomes (e.g., AD Composite Score [ADCOMS]), enrollment of earlier populations, and innovative trial designs (e.g., Bayesian adaptive designs) are new features in recent clinical trials. DISCUSSION: Drug development continues robustly at all phases despite setbacks in several programs in the recent past. Continuing unmet needs require a commitment to growing and accelerating the pipeline. Elsevier 2019-07-09 /pmc/articles/PMC6617248/ /pubmed/31334330 http://dx.doi.org/10.1016/j.trci.2019.05.008 Text en © 2019 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Featured Article
Cummings, Jeffrey
Lee, Garam
Ritter, Aaron
Sabbagh, Marwan
Zhong, Kate
Alzheimer's disease drug development pipeline: 2019
title Alzheimer's disease drug development pipeline: 2019
title_full Alzheimer's disease drug development pipeline: 2019
title_fullStr Alzheimer's disease drug development pipeline: 2019
title_full_unstemmed Alzheimer's disease drug development pipeline: 2019
title_short Alzheimer's disease drug development pipeline: 2019
title_sort alzheimer's disease drug development pipeline: 2019
topic Featured Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6617248/
https://www.ncbi.nlm.nih.gov/pubmed/31334330
http://dx.doi.org/10.1016/j.trci.2019.05.008
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