新型口服小分子胰高血糖素样肽-1受体激动剂AZD0186的临床前评估和首次人体i期试验。

IF 3.8 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Weier Qi, Simina M Boca, Alessandro Boianelli, Monica Fredberg, Sara Lundqvist, Graeme Davies, Joss Field, Cheryl A Brighton, Arjan Snijder, Pernilla Grundevik, Daniel Eckernäs, Annika Maria Träff, Magnus Polla, Daniel Pettersen, Sami Omar, Lars Hansen, David Janzén, Johanna Melin, Natalie van Zuydam, Jennifer Logue, Kristina Wallenius
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引用次数: 0

摘要

小分子胰高血糖素样肽-1受体激动剂AZD0186被开发出来,为广泛的2型糖尿病和/或肥胖患者提供可获得和方便的治疗。我们描述了这种新型小分子胰高血糖素样肽-1受体激动剂的临床前和首次人体单次上升剂量数据(NCT05694741)。AZD0186在过表达人或食蟹胰高血糖素样肽-1受体(GLP-1R)的细胞系和人源性EndoC-βH5细胞中检测到。通过静脉葡萄糖耐量试验,对肥胖非人灵长类动物和人源化GLP-1R (hGLP-1R)小鼠进行葡萄糖刺激胰岛素分泌(GSIS)评估。评估口服重复给药对hGLP-1R小鼠体重和食物摄入量的影响。AZD0186在健康受试者中以4种口服单次上升剂量水平(5、15、50和150 mg)进行评估。结果表明,AZD0186对hGLP-1R有较强的抑制作用,且在内皮细胞(EndoC-βH5)中表现出浓度依赖性的GSIS增强(EC50 = 0.6 nM)。在静脉葡萄糖耐量试验后,肥胖的非人灵长类动物在所有3种剂量水平下胰岛素分泌均增强。hGLP-1R小鼠口服给药(每天25 mg/kg,每天2次)5天后,体重减轻9.9%±2.3%(平均±SD)。在健康参与者中,AZD0186耐受性良好,在150 mg时报告恶心,与GLP-1RA类效应保持一致。在整个剂量范围内,AZD0186在浓度-时间曲线下的面积近似呈剂量正比增加。中位终末半衰期为1.95 ~ 7.58小时。研究结果表明AZD0186是GLP-1R的有效激动剂,首次人体研究表明其具有良好的安全性和耐受性。意义声明:AZD0186是一种新型小分子胰高血糖素样肽-1受体激动剂,允许口服给药。我们描述了AZD0186的临床前和首次人体单次上升剂量数据。研究结果表明,AZD0186是一种有效的人胰高血糖素样肽-1受体激动剂,在人胰高血糖素样肽-1受体小鼠模型中改善血糖控制并降低体重,并且在健康人类参与者中具有良好的安全性和耐受性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Preclinical evaluation and first-in-human phase 1 trial of AZD0186, a novel, oral small molecule glucagon-like peptide-1 receptor agonist.

Small molecule glucagon-like peptide-1 receptor agonist AZD0186 was developed to provide accessible and convenient treatment for a broad patient population with type 2 diabetes mellitus and/or obesity. We describe the preclinical and first-in-human single ascending dose data (NCT05694741) for this novel small molecule glucagon-like peptide-1 receptor agonist. AZD0186 was profiled in cell lines overexpressing human or cynomolgus glucagon-like peptide-1 receptor (GLP-1R) and in human-derived EndoC-βH5 cells. Glucose-stimulated insulin secretion (GSIS) was assessed following an intravenous glucose tolerance test in obese nonhuman primates and humanized GLP-1R (hGLP-1R) mice. Effects of oral repeated dosing on body weight and food intake were assessed in hGLP-1R mice. AZD0186 was evaluated at 4 oral single ascending dose levels (5, 15, 50, and 150 mg) in healthy participants. Results showed that AZD0186 is potent on the hGLP-1R and showed a concentration-dependent potentiation of GSIS in EndoC-βH5 cells (EC50 = 0.6 nM). Insulin secretion was enhanced in obese nonhuman primates at all 3 dose levels evaluated following an intravenous glucose tolerance test. In hGLP-1R mice, body weight was reduced 9.9% ± 2.3% (mean ± SD) following 5 days of oral dosing (25 mg/kg per day twice a day). In the healthy participants, AZD0186 was well tolerated, with nausea reported at 150 mg, in keeping with GLP-1RA class effects. Across the dose range, AZD0186 area under the concentration-time curve increased in an approximately dose-proportional manner. Median terminal half-life ranged from 1.95 to 7.58 hours. Findings demonstrate that AZD0186 is a potent agonist of the GLP-1R, and the first-in-human study indicates a favorable safety and tolerability profile. SIGNIFICANCE STATEMENT: AZD0186 is a novel small molecule glucagon-like peptide-1 receptor agonist that allows for oral dosing. We describe the preclinical and first-in-human single ascending dose data for AZD0186. The findings demonstrate that AZD0186 is a potent agonist of the human glucagon-like peptide-1 receptor, improves glucose control and reduces body weight in a human glucagon-like peptide-1 receptor mouse model, and has a favorable safety and tolerability profile in healthy human participants.

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来源期刊
CiteScore
6.90
自引率
0.00%
发文量
115
审稿时长
1 months
期刊介绍: A leading research journal in the field of pharmacology published since 1909, JPET provides broad coverage of all aspects of the interactions of chemicals with biological systems, including autonomic, behavioral, cardiovascular, cellular, clinical, developmental, gastrointestinal, immuno-, neuro-, pulmonary, and renal pharmacology, as well as analgesics, drug abuse, metabolism and disposition, chemotherapy, and toxicology.
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