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Rare adverse events are described, and cost is limited, however, the use of treatments of unproven or uncertain effects may divert attention from more useful interventions and other promising research questions
JAMA 2022;327:53445.ArticlePubMedPMC 36
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Eli Lilly has not announced a specific regulatory submission timeline, but Phase 3 completion and FDA filing would logically follow several years behind CagriSemas timeline
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