PuSH - Publikationsserver des Helmholtz Zentrums München

Finan, B.* ; Douros, J.D.* ; Goldwater, R.* ; Hansen, A.M.K.* ; Hjerpsted, J.B.* ; Hjøllund, K.R.* ; Kankam, M.K.* ; Knerr, P.J.* ; Konkar, A.* ; Mowery, S.A.* ; Müller, T.D. ; Nielsen, J.R.* ; Nygård, S.B.* ; Perez-Tilve, D.* ; Raun, K.* ; Yang, B.* ; Tschöp, M.H. ; DiMarchi, R.D.*

A once-daily GLP-1/GIP/glucagon receptor tri-agonist (NN1706) lowers body weight in rodents, monkeys and humans.

Mol. Metab. 96:102129 (2025)
DOI PMC
Open Access Gold möglich sobald Verlagsversion bei der ZB eingereicht worden ist.
Single molecules that combine complementary modes of action with glucagon-like peptide-1 receptor (GLP-1R) agonism are best-in-class therapeutics for obesity treatment. NN1706 (MAR423, RO6883746) is a fatty-acylated tri-agonist designed for balanced activity at GLP-1R and glucose-dependent insulinotropic polypeptide receptor (GIPR) with lower relative potency at the glucagon receptor (GcgR). Obese mice, rats and non-human primates dosed with NN1706 showed significant body weight reductions and improved glycemic control. In human participants with overweight or obesity, daily subcutaneous NN1706 treatment resulted in substantial body weight loss in a dose-dependent manner without impairing glycemic control (NCT03095807, NCT03661879). However, increased heart rate was observed across NN1706 treatment cohorts, which challenges further clinical development of NN1706.
Altmetric
Weitere Metriken?
Zusatzinfos bearbeiten [➜Einloggen]
Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Korrespondenzautor
Schlagwörter Clinical ; Glucagon ; Incretins ; Obesity
ISSN (print) / ISBN 2212-8778
e-ISSN 2212-8778
Zeitschrift Molecular Metabolism
Quellenangaben Band: 96, Heft: , Seiten: , Artikelnummer: 102129 Supplement: ,
Verlag Elsevier
Verlagsort Amsterdam
Nichtpatentliteratur Publikationen
Begutachtungsstatus Peer reviewed