Literature DB >> 31005596

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

John A Zebala1, Shawn L Searle2, Lynn R Webster2, Matt S Johnson3, Aaron D Schuler4, Dean Y Maeda4, Stuart J Kahn4.   

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.
Copyright © 2019 The Authors. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Desmetramadol; metabolism; poor metabolizer; tramadol; ultrarapid metabolizer

Year:  2019        PMID: 31005596      PMCID: PMC6790288          DOI: 10.1016/j.jpain.2019.04.005

Source DB:  PubMed          Journal:  J Pain        ISSN: 1526-5900            Impact factor:   5.820


  80 in total

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Journal:  Pain       Date:  2012-09-19       Impact factor: 6.961

5.  Differential sensitivity of three experimental pain models in detecting the analgesic effects of transdermal fentanyl and buprenorphine.

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6.  Discriminative stimulus effects of tramadol in humans.

Authors:  Angela N Duke; George E Bigelow; Ryan K Lanier; Eric C Strain
Journal:  J Pharmacol Exp Ther       Date:  2011-04-05       Impact factor: 4.030

7.  Impact of CYP2D6 genotype on postoperative tramadol analgesia.

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8.  Ticlopidine inhibits both O-demethylation and renal clearance of tramadol, increasing the exposure to it, but itraconazole has no marked effect on the ticlopidine-tramadol interaction.

Authors:  Nora M Hagelberg; Tuukka Saarikoski; Teijo I Saari; Mikko Neuvonen; Pertti J Neuvonen; Miia Turpeinen; Mika Scheinin; Kari Laine; Klaus T Olkkola
Journal:  Eur J Clin Pharmacol       Date:  2012-10-26       Impact factor: 2.953

9.  Comparative Toxicity of Tapentadol and Tramadol Utilizing Data Reported to the National Poison Data System.

Authors:  Ben T Tsutaoka; Raymond Y Ho; Stacey M Fung; Thomas E Kearney
Journal:  Ann Pharmacother       Date:  2015-09-14       Impact factor: 3.154

10.  Abuse liability of oxycodone as a function of pain and drug use history.

Authors:  S D Comer; M A Sullivan; S K Vosburg; W J Kowalczyk; J Houser
Journal:  Drug Alcohol Depend       Date:  2010-01-15       Impact factor: 4.492

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  2 in total

1.  Centrally administered CYP2D inhibitors increase oral tramadol analgesia in rats.

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Review 2.  Understanding Buprenorphine for Use in Chronic Pain: Expert Opinion.

Authors:  Lynn Webster; Jeffrey Gudin; Robert B Raffa; Jay Kuchera; Richard Rauck; Jeffrey Fudin; Jeremy Adler; Theresa Mallick-Searle
Journal:  Pain Med       Date:  2020-04-01       Impact factor: 3.750

  2 in total

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