Suppr超能文献

地美曲马多具有曲马多的安全性和镇痛特性,但没有其代谢方面的问题:连续随机、双盲、安慰剂和活性对照试验。

Desmetramadol Has the Safety and Analgesic Profile of Tramadol Without Its Metabolic Liabilities: Consecutive Randomized, Double-Blind, Placebo- and Active Comparator-Controlled Trials.

作者信息

Zebala John A, Searle Shawn L, Webster Lynn R, Johnson Matt S, Schuler Aaron D, Maeda Dean Y, Kahn Stuart J

机构信息

Syntrix Pharmaceuticals, Auburn, Washington.

PRA Health Sciences, Salt Lake City, Utah.

出版信息

J Pain. 2019 Oct;20(10):1218-1235. doi: 10.1016/j.jpain.2019.04.005. Epub 2019 Apr 18.

Abstract

Desmetramadol is an investigational analgesic consisting of (+) and (-) enantiomers of the tramadol metabolite O-desmethyltramadol (M1). Tramadol is racemic and exerts analgesia by monoaminergic effects of (-)-tramadol and (-)-M1, and by the opioid (+)-M1. Tramadol labeling indicates cytochrome P450 (CYP) isozyme 2D6 ultrarapid metabolizer can produce dangerous (+)-M1 levels, and CYP2D6 poor metabolizers insufficient (+)-M1 for analgesia. We hypothesized that desmetramadol could provide the safety and analgesia of tramadol without its metabolic liabilities. We conducted consecutive double-blind, randomized, placebo-controlled, 3 segment cross-over trials A and B to investigate the steady-state pharmacokinetics and analgesia of 20 mg desmetramadol and 50 mg tramadol in 103 healthy participants without (n = 43) and with (n = 60) cotreatment with the CYP inhibitor paroxetine. In the absence of CYP inhibition (trial A), 20 mg desmetramadol and 50 mg tramadol dosed every 6 hours gave equivalent steady-state (+)-M1, similar adverse events, and analgesia significantly greater than placebo, but equal to each other. In trial B, CYP inhibition significantly depressed tramadol steady-state (+)-M1, reduced its adverse events, and led to insignificant analgesia comparable with placebo. In contrast, CYP inhibition in trial B had no deleterious effect on desmetramadol (+)-M1 or (-)-M1, which gave significant analgesia as in trial A and superior to tramadol (P = .003). Desmetramadol has the safety and efficacy of tramadol without its metabolic liabilities. CLINICALTRIALS.GOV REGISTRATIONS: NCT02205554, NCT03312777 PERSPECTIVE: To our knowledge, this is the first study of desmetramadol in humans and the first to show it provides the same safety and analgesia as tramadol, but without tramadol's metabolic liabilities and related drug-drug interactions. Desmetramadol could potentially offer expanded safety and usefulness to clinicians seeking an alternative to schedule II opioids.

摘要

地美曲马多是一种研究中的镇痛药,由曲马多代谢物O - 去甲基曲马多(M1)的(+)和(-)对映体组成。曲马多是消旋体,通过(-)-曲马多和(-)-M1的单胺能效应以及阿片样物质(+)-M1发挥镇痛作用。曲马多的药品说明书指出,细胞色素P450(CYP)同工酶2D6超快代谢者可产生危险的(+)-M1水平,而CYP2D6慢代谢者产生的(+)-M1不足以产生镇痛效果。我们推测地美曲马多可以提供曲马多的安全性和镇痛效果,而不存在其代谢方面的问题。我们进行了连续的双盲、随机、安慰剂对照、三阶段交叉试验A和B,以研究20 mg地美曲马多和50 mg曲马多在103名健康参与者(43名未同时使用CYP抑制剂帕罗西汀,60名同时使用CYP抑制剂帕罗西汀)中的稳态药代动力学和镇痛效果。在没有CYP抑制的情况下(试验A),每6小时服用20 mg地美曲马多和50 mg曲马多产生的稳态(+)-M1相当,不良事件相似,镇痛效果显著优于安慰剂,但两者相当。在试验B中,CYP抑制显著降低了曲马多的稳态(+)-M1,减少了其不良事件,并导致与安慰剂相当的无显著意义的镇痛效果。相比之下,试验B中的CYP抑制对地美曲马多的(+)-M1或(-)-M1没有有害影响,其镇痛效果与试验A一样显著,且优于曲马多(P = 0.003)。地美曲马多具有曲马多的安全性和有效性,且不存在其代谢方面的问题。临床试验注册编号:NCT02205554,NCT03312777观点:据我们所知,这是首次在地美曲马多人体研究中表明它提供与曲马多相同的安全性和镇痛效果,但不存在曲马多的代谢问题及相关药物相互作用。地美曲马多可能为寻求替代II类阿片药物的临床医生提供更大的安全性和实用性。

相似文献

3
Inhibition of CYP2D6-mediated tramadol O-demethylation in methadone but not buprenorphine maintenance patients.
Br J Clin Pharmacol. 2012 Nov;74(5):835-41. doi: 10.1111/j.1365-2125.2012.04256.x.
4
Tramadol as a new probe for cytochrome P450 2D6 phenotyping: a population study.
Clin Pharmacol Ther. 2005 Jun;77(6):458-67. doi: 10.1016/j.clpt.2005.01.014.
5
The analgesic effect of tramadol after intravenous injection in healthy volunteers in relation to CYP2D6.
Anesth Analg. 2006 Jan;102(1):146-50. doi: 10.1213/01.ane.0000189613.61910.32.
7
Effects of terbinafine and itraconazole on the pharmacokinetics of orally administered tramadol.
Eur J Clin Pharmacol. 2015 Mar;71(3):321-7. doi: 10.1007/s00228-014-1799-2. Epub 2015 Jan 6.
8
Near-fatal tramadol cardiotoxicity in a CYP2D6 ultrarapid metabolizer.
Eur J Clin Pharmacol. 2011 Aug;67(8):855-8. doi: 10.1007/s00228-011-1080-x. Epub 2011 Jun 21.
9
Effects of the CYP2D6 gene duplication on the pharmacokinetics and pharmacodynamics of tramadol.
J Clin Psychopharmacol. 2008 Feb;28(1):78-83. doi: 10.1097/JCP.0b013e318160f827.
10
The hypoalgesic effect of tramadol in relation to CYP2D6.
Clin Pharmacol Ther. 1996 Dec;60(6):636-44. doi: 10.1016/S0009-9236(96)90211-8.

引用本文的文献

2
The Oxford Catalogue of Opioids: A systematic synthesis of opioid drug names and their pharmacology.
Br J Clin Pharmacol. 2021 Oct;87(10):3790-3812. doi: 10.1111/bcp.14786. Epub 2021 Mar 20.
3
Centrally administered CYP2D inhibitors increase oral tramadol analgesia in rats.
Brain Res Bull. 2020 Nov;164:400-406. doi: 10.1016/j.brainresbull.2020.09.001. Epub 2020 Sep 11.
4
Desmetramadol Is Identified as a G-Protein Biased µ Opioid Receptor Agonist.
Front Pharmacol. 2020 Jan 30;10:1680. doi: 10.3389/fphar.2019.01680. eCollection 2019.
5
Understanding Buprenorphine for Use in Chronic Pain: Expert Opinion.
Pain Med. 2020 Apr 1;21(4):714-723. doi: 10.1093/pm/pnz356.

本文引用的文献

2
Opioid Prescribing: What Are the Numbers?
Clin Pharmacol Drug Dev. 2018 Jan;7(1):6-8. doi: 10.1002/cpdd.430.
5
Vital Signs: Changes in Opioid Prescribing in the United States, 2006-2015.
MMWR Morb Mortal Wkly Rep. 2017 Jul 7;66(26):697-704. doi: 10.15585/mmwr.mm6626a4.
6
CDC Guideline for Prescribing Opioids for Chronic Pain--United States, 2016.
JAMA. 2016 Apr 19;315(15):1624-45. doi: 10.1001/jama.2016.1464.
7
Comparative Toxicity of Tapentadol and Tramadol Utilizing Data Reported to the National Poison Data System.
Ann Pharmacother. 2015 Dec;49(12):1311-6. doi: 10.1177/1060028015604631. Epub 2015 Sep 14.
8
Tramadol overdose causes seizures and respiratory depression but serotonin toxicity appears unlikely.
Clin Toxicol (Phila). 2015 Jul;53(6):545-50. doi: 10.3109/15563650.2015.1036279. Epub 2015 Apr 22.
9
A case of respiratory depression in a child with ultrarapid CYP2D6 metabolism after tramadol.
Pediatrics. 2015 Mar;135(3):e753-5. doi: 10.1542/peds.2014-2673. Epub 2015 Feb 2.
10
Interethnic variability of CYP2D6 alleles and of predicted and measured metabolic phenotypes across world populations.
Expert Opin Drug Metab Toxicol. 2014 Nov;10(11):1569-83. doi: 10.1517/17425255.2014.964204.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验