Discovery, development, and clinical proof of mechanism of LY3463251, a long-acting GDF15 receptor agonist

被引:53
作者
Benichou, Olivier [1 ]
Coskun, Tamer [2 ]
Gonciarz, Malgorzata D. [2 ]
Garhyan, Parag [2 ]
Adams, Andrew C. [2 ]
Du, Yu [2 ]
Dunbar, James D. [2 ]
Martin, Jennifer A. [2 ]
Mather, Kieren J. [2 ]
Pickard, Richard T. [2 ]
Reynolds, Vincent L. [2 ]
Robins, Deborah A. [2 ]
Zvada, Simbarashe P. [2 ]
Emmerson, Paul J. [2 ]
机构
[1] Eli Lilly & Co, F-92521 Neuilly sur seine, France
[2] Eli Lilly & Co, Indianapolis, IN 46285 USA
关键词
WEIGHT-LOSS; BARIATRIC SURGERY; OBESITY; INTERVENTION; METAANALYSIS; MAINTENANCE; OVERWEIGHT; APPETITE; ANOREXIA; NEEDS;
D O I
10.1016/j.cmet.2022.12.011
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
GDF15 and its receptor GFRAL/RET form a non-homeostatic system that regulates food intake and body weight in preclinical species. Here, we describe a GDF15 analog, LY3463251, a potent agonist at the GFRAL/RET receptor with prolonged pharmacokinetics. In rodents and obese non-human primates, LY3463251 decreased food intake and body weight with no signs of malaise or emesis. In a first-in-human study in healthy participants, single subcutaneous LY3463251 injections showed a safety and pharmacoki-netic profile supporting further clinical development with dose-dependent nausea and emesis in a subset of individuals. A subsequent 12-week multiple ascending dose study in overweight and obese participants showed that LY3463251 induced significant decreases in food intake and appetite scores associated with modest body weight reduction independent of nausea and emesis (clinicaltrials.gov: NCT03764774). These observations demonstrate that agonism of the GFRAL/RET system can modulate energy balance in humans, though the decrease in body weight is surprisingly modest, suggesting challenges in leveraging the GDF15 system for clinical weight-loss applications.
引用
收藏
页码:274 / +
页数:24
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