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They do not establish the efficacy of a 400 mcg SubQ dose in GLOW, and their findings cannot be assigned to a TB-500 fragment vial. Regulatory Status GLOW as a pre-mixed blend has not been evaluated by the FDA
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The findings confirm previous results from a Phase 2/3 trial and point to ultrahigh-dose methylcobalamin as a potential new therapy for early-stage ALS
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