Ligand Pharmaceuticals Incorporated LGND announced the presentation
of a poster titled “Glucagon Receptor Antagonist LGD-6972 Is Efficacious in
Streptozotocin-Induced Diabetic Mice” at the 73^rd Scientific Sessions of the
American Diabetes Association in Chicago. The poster provides data from
preclinical studies of Ligand's novel compound, LGD-6972, demonstrating
significant glucose lowering activity in an animal model of type 1 diabetes.
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.
“Glucagon receptor antagonism could play an important role in the treatment of
diabetes. Previous studies have demonstrated efficacy in models of type 2
diabetes and the present work shows utility for type 1 diabetes as well,”
commented Matthew W. Foehr, Executive Vice President and Chief Operating
Officer of Ligand. “Our glucagon program is an important example of the
diversity of partnered and unpartnered products making up Ligand's extensive
portfolio of assets. We plan to submit an IND for LGD-6972 in the second half
of 2013.”
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