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The company has not publicly confirmed a submission date, but its quarterly investor calls have consistently described retatrutide as a "late-stage pipeline priority." Lilly could also pursue a pre-NDA meeting with the FDA, where the agency provides informal guidance on what the application should contain
This design allows for convenient and easy swallowing, and provides a precise dosage of the active ingredients
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doi:10.1016/j.eurpsy.2011.05.004 Torrioli MG, Vernacotola S, Peruzzi L, et al
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