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Glutaryl-CoA dehydrogenase (GCDH) deficiency is an inborn error of lysine and tryptophan metabolism that results in increased formation and excretion of glutaric acid (GA), 3-hydroxyglutaric acid (3-OH-GA), glutaconic acid and glutarylcarnitine [82]

Store at room temperature (20-25C) before opening, and refrigerate (2-8C) after opening/reconstitution

By molecule class, the market is divided into semaglutide, tirzepatide, and other molecules

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Dosing rhythm: Start low, increase if tolerated, and time doses before meals