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The lack of studies means dosing protocols are speculative, side effect profiles unknown, and risks potentially severe - particularly gastroparesis from combined extreme gastric slowing
Endocrinology , 142(12), 5182-5189
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The first part of the study began by randomly dividing the test subjects in four groups including: wild type, APP/PS1, APP/PS1 + Dihexa administered at a dose of 1.44 mg/kg, and APP/PS1 + Dihexa administered at a dose of 2.88 mg/kg [1]
Amylin: From Mode of Action to Future Clinical Potential in Diabetes and Obesity
