新型口服黑素皮质素-1受体激动剂Dersimelagon潜在药物相互作用的评估。

IF 2.6 4区 医学 Q2 PHARMACOLOGY & PHARMACY Pharmacology Research & Perspectives Pub Date : 2025-02-01 DOI:10.1002/prp2.70069
Akihito Ogasawara, Ryosuke Ide, Shinsuke Inoue, Minoru Tsuda, Renli Teng
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引用次数: 0

摘要

Dersimelagon是一种新的实验性口服选择性激动剂的黑素皮质素-1受体。在非临床(体外)和临床研究中,研究了dersimelagon的药物-药物相互作用(DDI)潜力。研究了去皮霉素对CYP/UGT异构体和外排/摄取转运体的体外抑制作用。在一项1期研究中,研究了300 mg脱西乐根对底物药物药代动力学(PK)的影响,以及维拉帕米对100 mg脱西乐根(作为底物药物)药代动力学的影响。根据底物药物单独给药和与dersimelagon(或verapamil)联合给药的Cmax和AUC0-∞比值评估ddi。观察到皮霉根对CYP2C9、CYP3A、UGT1A1、BCRP、P-gp和oats的体外抑制作用相对较强。在临床研究中,阿托伐他汀(CYP3A、P-gp、BCRP、OATP底物)、瑞舒伐他汀(BCRP和OATP底物)和β-羟基辛伐他汀(辛伐他汀的代谢物)的暴露量增加2- 3倍(阿托伐他汀:Cmax LS平均比值= 198.0%;AUC0-∞比值= 196.6%;瑞舒伐他汀:Cmax比值= 316.5%,AUC0-∞比值= 206.0%)与dersimelagon合用。咪达唑仑(CYP3A底物)、地高辛(P-gp)、普伐他汀(OATP)和辛伐他汀(CYP3A)与dersimelagon合用时,未显示出任何临床相关的DDI效应。当与维拉帕米联合给药时,脱美良的暴露增加了~25%,这一效应被认为与临床无关。Dersimelagon 300 mg未引起涉及CYP/UGT酶和药物转运体的主要ddi;然而,dersimelagon可能与BCRP底物药物(如阿托伐他汀和瑞舒伐他汀)一起具有临床相关ddi的潜力,当与这些他汀类药物共同使用300 mg dersimelagon时应谨慎。试验注册:ClinicalTrials.gov: NCT04793295, NCT04402489, NCT04440592, NCT02834442, NCT03520036, NCT03503266。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Assessment of Potential Drug-Drug Interactions for Novel Oral Melanocortin-1 Receptor Agonist Dersimelagon.

Dersimelagon is a novel investigational orally administered selective agonist of the melanocortin-1 receptor. The drug-drug interaction (DDI) potential of dersimelagon was investigated in both nonclinical (in vitro) and clinical studies. The in vitro inhibition of CYP/UGT isoforms and efflux/uptake transporters by dersimelagon was assessed. The impact of 300-mg dersimelagon on the pharmacokinetics (PK) of substrate drugs and the effect of co-administering verapamil on 100-mg dersimelagon PK (as substrate drug) were investigated in healthy participants in a Phase 1 study. DDIs were assessed based on ratios of Cmax and AUC0-∞ of substrate drug administered alone and with dersimelagon (or verapamil). Relatively potent in vitro inhibition of CYP2C9, CYP3A, UGT1A1, BCRP, P-gp, and OATPs by dersimelagon was observed. In the clinical study, exposures of atorvastatin (CYP3A, P-gp, BCRP, OATP substrate) rosuvastatin (BCRP and OATP substrate), and β-hydroxy simvastatin (metabolite of simvastatin) increased 2- to 3-fold (atorvastatin: Cmax LS mean ratio = 198.0%; AUC0-∞ ratio = 196.6%; rosuvastatin: Cmax ratio = 316.5%, AUC0-∞ ratio = 206.0%) when co-administered with dersimelagon. Midazolam (CYP3A substrate), digoxin (P-gp), pravastatin (OATP), and simvastatin (CYP3A) did not show any clinically relevant DDI effects when co-administered with dersimelagon. Dersimelagon exposure increased ~25% when co-administered with verapamil, an effect not considered clinically relevant. Dersimelagon 300 mg did not elicit major DDIs involving CYP/UGT enzymes and drug transporters; however, dersimelagon may have potential for clinically relevant DDIs with drugs that are substrates for BCRP, such as atorvastatin and rosuvastatin, and caution should be exercised when co-administering 300-mg dersimelagon with these statin drugs. Trial Registration: ClinicalTrials.gov: NCT04793295, NCT04402489, NCT04440592, NCT02834442, NCT03520036, NCT03503266.

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来源期刊
Pharmacology Research & Perspectives
Pharmacology Research & Perspectives Pharmacology, Toxicology and Pharmaceutics-General Pharmacology, Toxicology and Pharmaceutics
CiteScore
5.30
自引率
3.80%
发文量
120
审稿时长
20 weeks
期刊介绍: PR&P is jointly published by the American Society for Pharmacology and Experimental Therapeutics (ASPET), the British Pharmacological Society (BPS), and Wiley. PR&P is a bi-monthly open access journal that publishes a range of article types, including: target validation (preclinical papers that show a hypothesis is incorrect or papers on drugs that have failed in early clinical development); drug discovery reviews (strategy, hypotheses, and data resulting in a successful therapeutic drug); frontiers in translational medicine (drug and target validation for an unmet therapeutic need); pharmacological hypotheses (reviews that are oriented to inform a novel hypothesis); and replication studies (work that refutes key findings [failed replication] and work that validates key findings). PR&P publishes papers submitted directly to the journal and those referred from the journals of ASPET and the BPS
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