FDA allows MabionCD20 as first-line therapy, trial shortened to 24 weeks
Published 23 h ago1 sourceEvidence: Reported
A bipartisan group of lawmakers is pressing the FDA to close a regulatory loophole that allows importation of counterfeit versions of Eli Lilly's investigational obesity drug retatrutide. The move signals growing concern over unregulated peptide imports and potential safety risks, though the FDA's response remains uncertain. This could impact the market for legitimate obesity treatments and regulatory enforcement.
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