Trace Launches With $101m To Pursue ALS Drug Based On Genomic Insights

Could Address Up To 97% Of Patients

Trace Neuroscience will take its antisense oligonucleotide that restores UNC13A protein production through proper mRNA splicing into the clinic in early 2026.

Trace's lead drug candidate targets UNC13A mRNA splicing to treat ALS (Shutterstock)

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