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The drugmaker stated that Orforgliprons positive Phase 3 ATTAIN-1 trial results have put it on track to submit to global regulatory agencies by the end of 2025

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[0007] WO2007/0611434 described pharmaceutical compositions of intranasal exenatide using similar formulation technologies in WO2007/146488, plus a dipeptidyl aminopeptidase (DPP) IV inhibitor to minimize enzymatic degradation of exenatide