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A randomised, open-label, two-cohort, three-period, crossover, single-dose bioavailability study evaluating the pharmacokinetics of Tramadol and Celecoxib at three dose levels following administration of a co-crystal entity in Japanese and Caucasian healthy volunteers

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Trial Profile

A randomised, open-label, two-cohort, three-period, crossover, single-dose bioavailability study evaluating the pharmacokinetics of Tramadol and Celecoxib at three dose levels following administration of a co-crystal entity in Japanese and Caucasian healthy volunteers

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 22 Jul 2018

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At a glance

  • Drugs Celecoxib/tramadol (Primary)
  • Indications Pain
  • Focus Pharmacokinetics
  • Sponsors Mundipharma Research

    • Most Recent Events

    • 28 Jun 2018 This trial was conducted a contract research organisation (Richmond Pharmacology Ltd).
    • 28 Jun 2018 Results published in the European Journal of Drug Metabolism and Pharmacokinetics
    • 20 Nov 2016 New trial record

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