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The FDA said Friday that it will start taking action against compounders for violations in the next 60 to 90 days, depending on the type of facility, in order to "avoid unnecessary disruption to patient treatment." "Now that the FDA has determined the drug shortage for semaglutide has been resolved, we will continue to offer access to personalized treatments as allowed by law to meet patient needs," Hims & Hers CEO Andrew Dudum posted Friday on X

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At the functional level, a major knowledge gap lies in distinguishing whether mtDNA mutations act as oncogenic drivers or merely represent passenger events

C-terminal interactions mediate the quaternary dynamics of B-crystallin