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US Food and Drug Administration (FDA) regulations allow human drug compounding in which licensed pharmacists or physicians can combine, mix, or adjust the ingredients of a medication to meet patient needs when popular branded formulations are in short supply.

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These data are expected to further validate HM17321s potential as a first-in-class treatment offering a fundamentally differentiated mechanism of action from current GLP-1 therapies.Beyond its monotherapy potential, HM17321 has also demonstrated additive efficacy when used in combination with incretin-based agents, further expanding its versatility as a next-generation obesity solution
