Positive Phase III results across the board for Zealand Pharma AS's dasiglucagon as a ready-to-use prefilled syringe rescue medication for severe hypoclyemia put the drug on track for a US FDA filing in the second half of 2019, but far behind two competing products that are already under review – Eli Lilly & Co.'s needle-free nasal product AMG504-1 and Xeris Pharmaceuticals Inc.'s XeriSol glucagon autoinjector.
Dasiglucagon (glucagon analog stable in liquid formulation) will be delivered in Zealand's ready-to-use HypoPal autoinjector rescue pen
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