Listening session with the US Food and Drug Administration, Lewy Body Dementia Association, and an expert panel.

ABSTRACT: The regulatory path for drug approval is increasingly well defined. Drugs for the treatment of Alzheimer disease (AD) need to show statistically significant benefit over placebo with respect to cognitive and functional measures, with the Clinical Dementia Rating scale and Alzheimer's Disease Assessment Scale-Cognitive Subscale being among the most often used instruments in AD clinical trials. In contrast, there are no validated instruments for use in clinical trials of drugs for the treatment of dementia with Lewy bodies. This poses challenges for drug development because the regulatory pathway to drug approval requires demonstrable efficacy measures. In December 2021, the Lewy Body Dementia Association advisory group met with representatives from the US Food and Drug Administration to dis

SUBMITTER: Sabbagh MN 

PROVIDER: S-EPMC9983146 | biostudies-literature | 2023 Jan-Mar

REPOSITORIES: biostudies-literature