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& Pantel, K

(1996) reported the analog was 1.5-2x more potent than equimolar IGF-1 in catabolic rat models, and broader pharmacology literature places it at roughly 3x potency overall

GhoshTSRampelliSJefferyIBSantoroANetoMCapriMet al

By resisting binding to IGF-binding proteins (IGFBPs), IGF-1 LR3 remains free in the bloodstream longer, which increases its ability to activate IGF-1 receptors in muscle tissue