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Engaging all three pathways simultaneously drives glucose-dependent insulin secretion through the two incretin arms while adding glucagon-receptor agonism implicated in energy expenditure, the pharmacological rationale that distinguishes it from single (GLP-1 (Sema)) and dual (GLP-2 (Triz)) incretin agonists

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Diabetic rats treated for 42 d with a daily dose of 300 mg/kg of porcine skin gelatin showed their plasma glucose AUC reduced from 30 000 to 28 000 mg min/dl (1665 to 1554 mmol min/l), insulin levels increased 2-fold, active GLP-1 levels reduced from 15 to 135 pm and DPP4 activity reduced by half (Reference Huang, Hung and Jao48)

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