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Zenagamtide是一种新型的长效单分子GLP-1和胰淀素受体激动剂不会延缓胃排空.pdf

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1、1Novo Nordisk A/S,Sborg,Denmark;2Novo Nordisk Service Centre India Private Ltd,Bangalore,India;3Altasciences Inc.,Montreal,QC,Canada.This study was sponsored by Novo Nordisk A/S and is registered with ClinicalTrials.gov(NCT06461039).Medical writing support was provided by Donna Kennedy,PhD,of Apollo

2、,OPEN Health Communications,and funded by Novo Nordisk A/S,in accordance with Good Publication Practice(GPP)guidelines(ismpp.org/gpp-2022).MBNG is an employee of Novo Nordisk A/S.Presented at the 33rd European Congress on Obesity(ECO),1215 May 2026,Istanbul,Trkiye.References:(1)Sanyal AJ et al.N Eng

3、l J Med 2025;392:20892099;(2)Perkovic V et al.N Engl J Med;2024;391:109121;(3)Wilding JPH et al.N Engl J Med 2021;384:9891002;(4)Lincoff AM et al.N Engl J Med 2023;389:22212232;(5)Kosiborod MN et al.N Engl J Med 2023;389:10691084;(6)Lutz TA.Appetite 2022;172:105965;(7)Gasiorek A et al.Lancet 2025;40

4、6:135148;(8)Dahl K et al.Lancet 2025;406:149162;(9)Kuhre RE et al.EBioMedicine 2025;118;105862;(10)Lutz TA.Neuropharmacology 2025;278:110587;(11)Friedrichsen M et al.Diabetes Obes Metab 2021;23:754762.Zenagamtide,a novel,long-acting,unimolecular GLP-1 and amylin receptor agonist,does not delay gastr

5、ic emptyingMaria B.N.Gabe1,Ruben Duque do Vale1,Swathi Gopal2,Tobias Karlsson1,Gaetano Morelli3,Anne Flint1PO4.219https:/ QR code or visit the website below for:PosterPoster+slidesAim To evaluate the effect of oral and subcutaneous(s.c.)zenagamtide on gastric emptying.Introduction Glucagon-like pept

6、ide-1(GLP-1)receptor agonists have demonstrated clinically significant reductions in body weight and additional benefits,including reductions in cardiovascular risk and improvements in outcomes in people with heart failure,chronic kidney disease and metabolic dysfunction-associated steatohepatitis.1

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1. **研究目的**:评估口服和皮下注射zenagamtide(GLP-1、amylin和calcitonin受体激动剂)对胃排空的影响。 2. **核心数据**: - 口服zenagamtide(50mg稳态)与基线相比,对乙酰氨基酚AUC₀₋₆₀min比值0.92(95% CI: 0.80-1.07),AUC₀₋₃₀₀min比值1.16(1.10-1.21),Cmax比值1.03(0.94-1.13)。 - 皮下zenagamtide(20mg稳态)AUC₀₋₆₀min比值1.11(0.96-1.28),AUC₀₋₃₀₀min比值1.30(1.23-1.38),Cmax比值1.27(1.14-1.40)。 3. **结论**:两种给药方式均未延迟胃排空,降低与口服药物相互作用风险,安全性符合GLP-1/amylin受体激动剂特征。
**Zenagamtide效果如何?** **胃排空会延迟吗?** **药物相互作用风险低?**
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