Recommendations to address key recruitment challenges of Alzheimer's disease clinical trials
Jessica B Langbaum1, Julie Zissimopoulos2, Rhoda Au3
1Banner Alzheimer's Institute, Phoenix, Arizona, USA.
Abstract:
Clinical trials for Alzheimer's disease (AD) are slower to enroll study participants, take longer to complete, and are more expensive than trials in most other therapeutic areas. The recruitment and retention of a large number of qualified, diverse volunteers to participate in clinical research studies remain among the key barriers to the successful completion of AD clinical trials. An advisory panel of experts from academia, patient-advocacy organizations, philanthropy, non-profit, government, and industry convened in 2020 to assess the critical challenges facing recruitment in Alzheimer's clinical trials and develop a set of recommendations to overcome them. This paper briefly reviews existing challenges in AD clinical research and discusses the feasibility and implications of the panel's recommendations for actionable and inclusive solutions to accelerate the development of novel therapies for AD.
Insights
Recruiting participants for Alzheimer's disease (AD) clinical trials is challenging. This paper reviews expert recommendations to improve participant recruitment and retention for faster AD therapy development.
Area of Science:
- Neurology
- Clinical Research
- Public Health
Background:
- Alzheimer's disease (AD) clinical trials face significant hurdles in participant enrollment, duration, and cost compared to other therapeutic areas.
- Key barriers include recruiting and retaining sufficient numbers of qualified and diverse volunteers for AD research.
- These challenges impede the timely completion of clinical studies and the development of new AD treatments.
Purpose of the Study:
- To assess critical challenges in Alzheimer's disease clinical trial recruitment.
- To develop actionable and inclusive recommendations to overcome these recruitment barriers.
- To accelerate the development of novel therapies for Alzheimer's disease.
Main Methods:
- Convened an expert advisory panel in 2020 with diverse representation (academia, patient advocacy, government, industry).
- Reviewed existing challenges in AD clinical research participant recruitment and retention.
- Discussed feasibility and implications of panel-generated recommendations for AD clinical trials.
Main Results:
- Identified significant barriers to participant enrollment and retention in AD clinical trials.
- Proposed a set of recommendations from a multidisciplinary expert panel.
- Highlighted the need for actionable and inclusive solutions to accelerate AD research.
Conclusions:
- Addressing recruitment and retention challenges is crucial for successful AD clinical trials.
- Expert recommendations offer a pathway to overcome barriers and speed up therapeutic development.
- Implementing inclusive strategies can enhance diversity and efficiency in AD research.
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