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Description
American Journal of Clinical Nutrition

The design works because the GLP-1 and GIP arms buffer that glucose-raising tendency, leaving glucagon free to do something useful: push up energy expenditure, encourage the liver to burn its own fat stores, and increase the rate at which the body turns over lipids

For instance, when initiating GLP-1 therapy, a gradual reduction in insulin doses can help prevent diabetic ketoacidosis

No one taking placebo quit the trial early

Taylor Cottle, PhD Serial Biotech Entrepreneur| PhD, John Hopkins University

Glucagon-Like Peptide-1 Agonism : Retatrutide incorporates specific alpha-aminobutyric acid substitutions at critical nodes along its amino acid chain
