Highlights of the presentation include:
LGD-6972 is a potent and selective antagonist of the glucagon receptor (GCGR) that has previously demonstrated activity in pre-clinical models of type 2 diabetes
LGD-6972 significantly lowered fasting and non-fasting glucose levels in a mouse model of type 1 diabetes
LGD-6972 reduced HbA1c, ketone bodies, and free fatty acids in diabetic mice
LGD-6972 had additive effects when used in combination with insulin therapy and may be useful in an insulin sparing regimen
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