Gene Therapy Targeting SARM1 May Inhibit Neuron Degeneration in ALS, Mouse Study Shows

A gene therapy designed to block the activity of SARM1 protein prevented the loss of axons ­­­­— long projections that connect nerve cells and transport information ­­­­— making the therapy a potential strategy to reduce the loss of peripheral nerves in several neurodegenerative diseases, including amyotrophic lateral sclerosis (ALS), according to a mouse…

SARM1 Inhibition Has Potential to Prevent Neurodegeneration in ALS, Other Diseases, Preclinical Results Suggest

Inhibition of the SARM1 gene can prevent the degeneration of nerve cells in the central, ocular, and peripheral nervous system in mice, results from preclinical studies show. These findings provide evidence for the use of small-molecule inhibitors of the SARM1 protein being developed by Disarm Therapeutics as potential disease-modifying therapeutics for…