Evidence map›Paper›PMID 31005596›Full record

Trial reportThe journal of pain2019

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

3 registry-linked trialsOpen access · bronzeAbstract readRandomized Controlled Trial
In one paragraph

Trial report in The journal of pain, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 3 registered trials, which are not on this map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.4field-weighted citation impact, top 14% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT02205554 phase1completednot on this map

A Phase 1 Randomized, Double-Blind, Placebo-Controlled, Triple Cross-Over Study Investigating The Safety, Oral Steady-State Pharmacokinetics, And Clinical Activity Of 20 Mg Omnitram And 50 Mg Tramadol In Normal Human Subjects

TypeinterventionalSponsorSyntrix Biosystems, Inc.Ran2014 to 2014Enrolled43ConditionsPainArmsOmnitram, Tramadol, Placebo
NCT03312777 phase1completednot on this map

A Phase 1b, Double-Blind, Randomized, Placebo-Controlled, Three Segment Cross-Over Study Investigating Oral Steady-State Pharmacokinetics And Hypoalgesic Effect Of 20 Mg Omnitram And 50 Mg Tramadol In Normal Human Subjects Made Cyp2d6 Deficient By Paroxetine

TypeinterventionalSponsorSyntrix Biosystems, Inc.Ran2017 to 2017Enrolled60ConditionsPainArmsOmnitram, Tramadol, Placebo
NCT04683926 phase1completednot on this mapstarted 2021, after this paper: background citation

A Phase 1 Randomized Single Oral Dose Cross-Over Study Investigating Desmetramadol Dose Proportionality And Food Effect In Normal Human Subjects

TypeinterventionalSponsorSyntrix Biosystems, Inc.Ran2021 to 2021Enrolled24ConditionsPainArmsDesmetramadol
3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. New Insights on Tramadol and Immunomodulation.Current oncology reports · 2021
    Review
  5. Article
  6. Review
  7. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

John A ZebalaSyntrix Pharmaceuticals, Auburn, Washington. Electronic address: jzebala@syntrixbio.com.
Shawn L SearlePRA Health Sciences, Salt Lake City, Utah.
Lynn R WebsterPRA Health Sciences, Salt Lake City, Utah.
Matt S JohnsonDF/Net Research, Seattle, Washington.
Aaron D SchulerSyntrix Pharmaceuticals, Auburn, Washington.
Dean Y MaedaSyntrix Pharmaceuticals, Auburn, Washington.
Stuart J KahnSyntrix Pharmaceuticals, Auburn, Washington.
Syntrix Biosystems (United States) · USPRA Health Sciences · US

Funding

Overcoming Tramadol Resistance In CYP2D6 Poor Metabolizers: A Phase 1 Trial Demonstrating Analgesic Superiority of Omnitram to Tramadol in Subjects Coadministered ParoxetineR44DA027304 · NIDA · SYNTRIX BIOSYSTEMS, INC. · PI KAHN, STUART J, ZEBALA, JOHN A · 2012 to 2018
$5.1M
Overcoming Tramadol Resistance In CYP2D6 Poor MetabolizersR43DA027304 · NIDA · SYNTRIX BIOSYSTEMS, INC. · PI KAHN, STUART J, ZEBALA, JOHN A · 2010 to 2010
$650k
NIDA NIH HHS R43 DA027304NIDA NIH HHS R44 DA027304
6 · The paper itself

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.

Indexed as

AdultAnalgesics, OpioidCytochrome P-450 CYP2D6Double-Blind MethodFemaleHumansMalePain PerceptionTramadolYoung AdultAnalgesics, OpioidCytochrome P-450 CYP2D6O-demethyltramadolTramadolDesmetramadolmetabolismpoor metabolizertramadolultrarapid metabolizer

Identifiers

PMID31005596
PMCPMC6790288
OpenAlexW2936720839

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.