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(57) first reported dramatic improvement in PsO symptoms in a 73-year-old patient who had previously been unresponsive to biologic therapy

[5] Safety information: FDA said the available safety information was insufficient to characterize the safety profile for the proposed forms and routes, while reports in the adverse-event database were too limited and confounded to establish causality

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The discussion delved into the robust pipeline of GLP1 drugs, highlighting that companies like Eli Lilly and Novo Nordisk have over 80 drugs in trials within this category