Senators again point to AbbVie as a poster child for reform. Only this time Dems are targeting a low, low tax rate – Endpoints News

ALS is a debilitating, universally fatal disease. As motor neurons die, patients lose their abilities to walk, cut their own food, swallow and eventually, breathe. Most patients die within three to five years of symptom onset, and there are few approved treatments that only modestly impact function and survival.
Though patients and advocates have rallied around an experimental drug from Amylyx Pharmaceuticals, currently being reviewed by the FDA, they continue to emphasize how more work needs to be done. Research into ALS pathology remains scant relative to other fields, as scientists have yet to discover a confirmed biomarker that measures patients’ progress and have only identified a handful of genetic targets implicated in the disease.

Keep reading Endpoints with a free subscription
Unlock this story instantly and join 145,100+ biopharma pros reading Endpoints daily — and it’s free.


Leave a Comment

Your email address will not be published. Required fields are marked *