Zebala John A, Searle Shawn L, Webster Lynn R, Johnson Matt S, Schuler Aaron D, Maeda Dean Y, Kahn Stuart J
Syntrix Pharmaceuticals, Auburn, Washington.
PRA Health Sciences, Salt Lake City, Utah.
J Pain. 2019 Oct;20(10):1218-1235. doi: 10.1016/j.jpain.2019.04.005. Epub 2019 Apr 18.
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.
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。