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Whether this is clinically meaningful enough to suppress ipamorelin-induced GH release is not established in a controlled trial, but the mechanism is plausible

doi:10.1093/ajh/hpy082 Floras JS

This may have definite clinical applications regarding the actions of the PPAR agonist family of fibric acid, as well as the PPAR agonists: TDZs (rosiglitazone and pioglitazone currently in clinical use)