Research on treatment of ALS associated with the SOD1 gene mutation

https://www.sciencedaily.com/releases/2019/05/190501161224.htm

I came across this article on Science Daily website. It discusses a possible treatment for people with fALS due to a mutated SOD1 gene. It is similar to an article recently published on the ALS News Today website. 

“An early stage trial of an investigational therapy for amyotrophic lateral sclerosis (ALS) suggests that people could tolerate the experimental drug and, in exploratory results, the experimental drug was linked to possible slower progression in people with a genetic form of the disease caused by mutations in a gene called superoxide dismutase 1 (SOD1). The preliminary study released today will be presented at the American Academy of Neurology’s 71st Annual Meeting in Philadelphia, May 4 to 10, 2019.”  To read the rest of the article follow the link https://www.sciencedaily.com/releases/2019/05/190501161224.htm

Are there articles that you would like to share on our forum? What direction do you think ALS research should take?

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