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Cangene wins US FDA nod for botulism antitoxin

This article was originally published in Scrip

Executive Summary

Canadian biopharma Cangene won the US FDA's nod on 22 March to market the firm's botulism antitoxin (Equine), heptavalent (A, B, C, D, E, F, G) to treat patients with symptomatic botulism following suspected or documented exposure to botulinum neurotoxin.



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