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An Open-label, Randomized, Single-dose, Parallel-group Study to Investigate the PK Profile of Single Dose Buprenorphine Transdermal Patch 20 mg Applied for 3 Days, 40 mg for 3 Days and 40 mg for 4 Days in Chinese Subjects With Chronic Pain

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Trial Profile

An Open-label, Randomized, Single-dose, Parallel-group Study to Investigate the PK Profile of Single Dose Buprenorphine Transdermal Patch 20 mg Applied for 3 Days, 40 mg for 3 Days and 40 mg for 4 Days in Chinese Subjects With Chronic Pain

Status: Recruiting
Phase of Trial: Phase I

Latest Information Update: 14 Dec 2022

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At a glance

  • Drugs Buprenorphine (Primary) ; Naltrexone
  • Indications Pain
  • Focus Pharmacokinetics
  • Sponsors Mundipharma (China) Pharmaceutical

    • Most Recent Events

    • 03 Jun 2021 According to ClinicalTrials.gov, the recruitment status of this study is unknown because the information has not been verified recently (last verified June 2019).
    • 07 Jun 2019 New trial record

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