{"title":"†Obicetrapib 不会在脂肪组织中蓄积:人和非人灵长类动物的研究结果","authors":"","doi":"10.1016/j.jacl.2024.04.099","DOIUrl":null,"url":null,"abstract":"<div><h3>Study Funding</h3><p>NewAmsterdam Pharma.</p></div><div><h3>Background/Synopsis</h3><p>Previous CETP inhibitors were highly lipophilic with logP of 7.2–9.2, leading to adipose tissue accumulation in the case of anacetrapib. In contrast, obicetrapib is characterized by a logP of 4.9 and terminal half-life of ∼135 hours.</p></div><div><h3>Objective/Purpose</h3><p>Studies in cynomolgus monkeys and humans were undertaken to determine the definitive elimination of obicetrapib from these organisms.</p></div><div><h3>Methods</h3><p>In a 9-month toxicology study in cynomolgus monkeys, obicetrapib was administered at doses up to 50 mg/kg/day. A phase 1 trial administered doses of 1-25 mg to healthy humans, and 3, placebo-controlled, phase 2 studies in dyslipidemic humans administered obicetrapib (on background statin therapy) at 5 or 10 mg/d for 8 weeks (ROSE; n=120), 10 mg/d monotherapy or with ezetimibe for 12 weeks (ROSE2; n=119), and 2.5, 5, or 10 mg/d for 8 weeks (Japan; n=102). Plasma concentrations of obicetrapib were measured during dosing/treatment and up to 15-weeks post-treatment.</p></div><div><h3>Results</h3><p>In monkeys, obicetrapib was not detected in any adipose tissue samples and a recovery period of 13 weeks was sufficient for complete elimination from systemic circulation. The terminal half-life of obicetrapib was between 121 and 151 hours in healthy humans. In ROSE, median plasma obicetrapib in the 10 mg/d group was 384 mg/L at week 8 and decreased by 93, 98, and 99% at 4-, 8-, and 15-weeks post-treatment. In ROSE2, median plasma obicetrapib at week 12 was 387 mg/L in the 10 mg/d monotherapy group and decreased by 94% at 4-weeks post-treatment. In the Japan phase 2 study, median plasma obicetrapib at week 8 was 472 mg/L for the 10 mg/d group and decreased by 96% at 4-weeks post-treatment.</p></div><div><h3>Conclusions</h3><p>In dedicated pre-clinical experiments and in clinical trials, obicetrapib shows no evidence of accumulation in adipose tissue or delayed elimination from the systemic circulation supporting once daily, chronic dosing of 10 mg.</p></div>","PeriodicalId":15392,"journal":{"name":"Journal of clinical lipidology","volume":null,"pages":null},"PeriodicalIF":3.6000,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"†Obicetrapib Does Not Accumulate in Adipose Tissue: Results from Studies in Man and Non-human Primates\",\"authors\":\"\",\"doi\":\"10.1016/j.jacl.2024.04.099\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Study Funding</h3><p>NewAmsterdam Pharma.</p></div><div><h3>Background/Synopsis</h3><p>Previous CETP inhibitors were highly lipophilic with logP of 7.2–9.2, leading to adipose tissue accumulation in the case of anacetrapib. In contrast, obicetrapib is characterized by a logP of 4.9 and terminal half-life of ∼135 hours.</p></div><div><h3>Objective/Purpose</h3><p>Studies in cynomolgus monkeys and humans were undertaken to determine the definitive elimination of obicetrapib from these organisms.</p></div><div><h3>Methods</h3><p>In a 9-month toxicology study in cynomolgus monkeys, obicetrapib was administered at doses up to 50 mg/kg/day. A phase 1 trial administered doses of 1-25 mg to healthy humans, and 3, placebo-controlled, phase 2 studies in dyslipidemic humans administered obicetrapib (on background statin therapy) at 5 or 10 mg/d for 8 weeks (ROSE; n=120), 10 mg/d monotherapy or with ezetimibe for 12 weeks (ROSE2; n=119), and 2.5, 5, or 10 mg/d for 8 weeks (Japan; n=102). Plasma concentrations of obicetrapib were measured during dosing/treatment and up to 15-weeks post-treatment.</p></div><div><h3>Results</h3><p>In monkeys, obicetrapib was not detected in any adipose tissue samples and a recovery period of 13 weeks was sufficient for complete elimination from systemic circulation. The terminal half-life of obicetrapib was between 121 and 151 hours in healthy humans. In ROSE, median plasma obicetrapib in the 10 mg/d group was 384 mg/L at week 8 and decreased by 93, 98, and 99% at 4-, 8-, and 15-weeks post-treatment. In ROSE2, median plasma obicetrapib at week 12 was 387 mg/L in the 10 mg/d monotherapy group and decreased by 94% at 4-weeks post-treatment. In the Japan phase 2 study, median plasma obicetrapib at week 8 was 472 mg/L for the 10 mg/d group and decreased by 96% at 4-weeks post-treatment.</p></div><div><h3>Conclusions</h3><p>In dedicated pre-clinical experiments and in clinical trials, obicetrapib shows no evidence of accumulation in adipose tissue or delayed elimination from the systemic circulation supporting once daily, chronic dosing of 10 mg.</p></div>\",\"PeriodicalId\":15392,\"journal\":{\"name\":\"Journal of clinical lipidology\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":3.6000,\"publicationDate\":\"2024-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of clinical lipidology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1933287424001466\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"PHARMACOLOGY & PHARMACY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of clinical lipidology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1933287424001466","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
†Obicetrapib Does Not Accumulate in Adipose Tissue: Results from Studies in Man and Non-human Primates
Study Funding
NewAmsterdam Pharma.
Background/Synopsis
Previous CETP inhibitors were highly lipophilic with logP of 7.2–9.2, leading to adipose tissue accumulation in the case of anacetrapib. In contrast, obicetrapib is characterized by a logP of 4.9 and terminal half-life of ∼135 hours.
Objective/Purpose
Studies in cynomolgus monkeys and humans were undertaken to determine the definitive elimination of obicetrapib from these organisms.
Methods
In a 9-month toxicology study in cynomolgus monkeys, obicetrapib was administered at doses up to 50 mg/kg/day. A phase 1 trial administered doses of 1-25 mg to healthy humans, and 3, placebo-controlled, phase 2 studies in dyslipidemic humans administered obicetrapib (on background statin therapy) at 5 or 10 mg/d for 8 weeks (ROSE; n=120), 10 mg/d monotherapy or with ezetimibe for 12 weeks (ROSE2; n=119), and 2.5, 5, or 10 mg/d for 8 weeks (Japan; n=102). Plasma concentrations of obicetrapib were measured during dosing/treatment and up to 15-weeks post-treatment.
Results
In monkeys, obicetrapib was not detected in any adipose tissue samples and a recovery period of 13 weeks was sufficient for complete elimination from systemic circulation. The terminal half-life of obicetrapib was between 121 and 151 hours in healthy humans. In ROSE, median plasma obicetrapib in the 10 mg/d group was 384 mg/L at week 8 and decreased by 93, 98, and 99% at 4-, 8-, and 15-weeks post-treatment. In ROSE2, median plasma obicetrapib at week 12 was 387 mg/L in the 10 mg/d monotherapy group and decreased by 94% at 4-weeks post-treatment. In the Japan phase 2 study, median plasma obicetrapib at week 8 was 472 mg/L for the 10 mg/d group and decreased by 96% at 4-weeks post-treatment.
Conclusions
In dedicated pre-clinical experiments and in clinical trials, obicetrapib shows no evidence of accumulation in adipose tissue or delayed elimination from the systemic circulation supporting once daily, chronic dosing of 10 mg.
期刊介绍:
Because the scope of clinical lipidology is broad, the topics addressed by the Journal are equally diverse. Typical articles explore lipidology as it is practiced in the treatment setting, recent developments in pharmacological research, reports of treatment and trials, case studies, the impact of lifestyle modification, and similar academic material of interest to the practitioner. While preference is given to material of immediate practical concern, the science that underpins lipidology is forwarded by expert contributors so that evidence-based approaches to reducing cardiovascular and coronary heart disease can be made immediately available to our readers. Sections of the Journal will address pioneering studies and the clinicians who conduct them, case studies, ethical standards and conduct, professional guidance such as ATP and NCEP, editorial commentary, letters from readers, National Lipid Association (NLA) news and upcoming event information, as well as abstracts from the NLA annual scientific sessions and the scientific forums held by its chapters, when appropriate.