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[DOI] [PMC free article] [PubMed] [Google Scholar] 121.Pettinelli P., Videla L.A
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JC: Writing review & editing, Writing original draft, Supervision, Investigation, Formal analysis, Data curation
The speed of orforglipron's clinical development from Phase 1 to regulatory submission, spanning approximately 5 years from first-in-human dosing to FDA submission, represents one of the fastest development timelines in obesity pharmacotherapy history
6 , 712.e11 (2014)
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