o-desmethyltramadol

Small moleculeexperimental

Desmetramadol, also known as O-desmethyltramadol (O-DSMT), is an opioid analgesic and the main active metabolite of tramadol. Tramadol is demethylated by the liver enzyme CYP2D6 to desmetramadol in the same way as codeine, and so similarly to the variation in effects seen with codeine, individuals who have a less active form of CYP2D6 will tend to have reduced analgesic effects from tramadol. Because desmetramadol itself does not need to be metabolized to induce an analgesic effect, it can be used in individuals with CYP2D6 inactivating mutations. — Wikipedia

Clinical trial activity

1 trials · 3 clinical orgs · 0 marketing orgs

Phase 1
0
Phase 2
1
Phase 3
0
Phase 4
0

Earliest trial started Oct 1, 2018 (NCT03664921)

Timeline

2010s

  1. Jan 1, 2018

    Earliest Phase 2 Sponsor(trial)

Indications

Mechanism of action

Chemistry & pharmacology

Oral

No

Parenteral

No

Topical

No

Sources

Also known as

  • o-desmethyltramadol

Clinical trials

NCT IDPhaseStart dateSponsor(s)
NCT03664921Phase 2Oct 1, 2018DF/Net Research, National Institute on Drug Abuse (NIDA), Syntrix Biosystems, Inc.
Showing 1 of 1 trials
Page 1 / 1

Organizations

Research & Development (3)

OrganizationOrg typeTrialsAs lead sponsorPhasesEarliest year
DF/Net ResearchFor profit1012018
National Institute on Drug Abuse (NIDA)Government1012018
Syntrix Biosystems, Inc.For profit1112018
3 organizations
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