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Effects of Rifampicin on the Pharmacokinetics and Pharmacodynamics of Sublingual and Intravenous Buprenorphine

19 november 2014 uppdaterad av: Mari Fihlman, Turku University Hospital

Effects of Rifampicin on the Pharmacokinetics and Pharmacodynamics of Sublingual and Intravenous Buprenorphine: A Four-phase Cross-over Study in Healthy Subjects.

This study is aimed to examine the possible interactions of sublingual and intravenous buprenorphine with rifampicin.

Studieöversikt

Status

Avslutad

Betingelser

Detaljerad beskrivning

Variability in drug response can be due to either pharmacokinetic or pharmacodynamic factors. The reasons why people differ in pharmacokinetics or pharmacodynamics are manifold and include, e.g., genetic factors, diseases, age and concomitantly administered drugs. Oxidation reactions are dominant in the metabolism of drugs and cytochrome P-450 enzymes (CYP) have been recognized as chief contributors. We have previously shown that drug interactions mediated by the inhibition of CYP enzymes may be of major clinical significance.Buprenorphine is a semisynthetic partial µ-opioid receptor agonist. In low doses, it is used in the treatment of moderate acute and chronic pain whereas in high doses, it is used in the management of opioid withdrawal symptoms and opioid addiction. It has high affinity for the µ-opioid receptor and its analgesic efficacy is 20-40 times that of morphine. It acts as an antagonist at the myy-opioid receptor and as an agonist at the myy-opioid receptor and opioid-like receptor (ORL-1).

Buprenorphine undergoes extensive first-pass metabolism and has low oral bioavailability of 15 %. Bioavailability following sublingual administration of buprenorphine is higher, 50-60 %. After high sublingual doses of buprenorphine (8-24 mg), peak plasma concentrations are reached in 1 hour and after low sublingual doses (0.4 mg) they are reached in approximately 3 h. Approximately two-thirds of a buprenorphine dose is excreted unchanged, and the rest is metabolized in the liver and intestinal wall. N-dealkylation of buprenorphine mainly via CYP3A but also CYP2C8 yields norbuprenorphine, and glucuronidation yields buprenorphine-3-glucuronide. Norbuprenorphine is excreted in the urine after subsequent conjugation. 80-90 % of buprenorphine is excreted by the biliary system and enterohepatic circulation.Although few interaction studies of high-dose buprenorphine and antiretrovirals have been conducted, the effect of CYP3A inducers on the pharmacokinetics of low-dose buprenorphine is unknown. Because the use of buprenorphine in pain management is increasing after the introduction of transdermal buprenorphin patches to the market, it is clinically relevant to study and quantify possible interactions of buprenorphine with inducers of its CYP3A-mediated metabolism such as rifampicin.

Studietyp

Interventionell

Inskrivning (Faktisk)

12

Fas

  • Fas 4

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studieorter

      • Turku, Finland, 20500
        • Turku University Hospital

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

18 år till 40 år (Vuxen)

Tar emot friska volontärer

Ja

Kön som är behöriga för studier

Allt

Beskrivning

Inclusion Criteria:

  • non-smoking
  • aged 18-40 years
  • body weights within ±15% of the ideal weight for height

Exclusion Criteria

  • A previous history of intolerance to the study drugs or to related compounds and additives.
  • Concomitant drug therapy of any kind for at least 14 days prior to the study.
  • Subjects younger than 18 years and older than 40 years.
  • Existing or recent significant disease.
  • History of hematological, endocrine, metabolic or gastrointestinal disease, including gut motility disorders.
  • History of asthma or any kind of drug allergy.
  • Previous or present alcoholism, drug abuse, psychological or other emotional problems that are likely to invalidate informed consent, or limit the ability of the subject to comply with the protocol requirements.
  • A positive test result for urine toxicology.
  • A "yes" answer to any one of the Abuse Questions.
  • Pregnancy or nursing.
  • Donation of blood for 4 weeks prior and during the study.
  • Special diet or life style conditions which would compromise the conditions of the study or interpretation of the results.
  • Participation in any other studies involving investigational or marketed drug products concomitantly or within one month prior to the entry into this study.
  • Smoking for one month before the start of the study and during the whole study period.

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Grundläggande vetenskap
  • Tilldelning: Randomiserad
  • Interventionsmodell: Crossover tilldelning
  • Maskning: Enda

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Aktiv komparator: Rifampicin
The volunteers will be given oral rifampicin (Rimapen, Orion, Finland) 600 mg as a single daily dose at 20.00 for 7 days
The volunteers will be given oral rifampicin (Rimapen, Orion, Finland) 600 mg as a single daily dose at 20.00 for 7 days
Placebo-jämförare: Placebo
The volunteers will be given oral placebo at 20.00 for 7 days
The volunteers will be given Oral placebo at 20.00 for 7 days [Phase 1 ]
Aktiv komparator: Buprenorphine
The volunteers will be given single dose of 0,4 mg intra venous buprenorphine or 0,6 mg sublingual buprenorphine on day 5.
The volunteers will be given single dose of 0,4 mg intra venous buprenorphine or 0,6 mg sublingual buprenorphine on day 5.
Andra namn:
  • Temgesic 0,2 mg resoriblet
  • Temgesic 0,3 mg/ml

Vad mäter studien?

Primära resultatmått

Resultatmått
Tidsram
Concentration of buprenorphine and its metabolites in plasma and urine concebtration of buprenorphine
Tidsram: 0.5, 1, 1.5, 2, 3, 4, 5, 6, 8, 10, 12 and 20 hours after administration of buprenorphine
0.5, 1, 1.5, 2, 3, 4, 5, 6, 8, 10, 12 and 20 hours after administration of buprenorphine

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Pharmacodynamic effects
Tidsram: 1, 2,3, 4, 5, 6, 8, 10, 12, 20 hours after administration of buprenorphine
The psychomotor effects on bubrenorphine will be assessed with the measurement of pupil size, Maddox wing test and symbol substitution test.
1, 2,3, 4, 5, 6, 8, 10, 12, 20 hours after administration of buprenorphine
Analgesia
Tidsram: 1, 2, 3, 4, 5, 6, 8, 10, 12 hours after the administration of buprenorphine
The analgesic effect of buprenorphine will be evaluated using the cold pressor test. The cold pain test has been shown to be sensitive to opioid analgesia, and it enables repeated assessments of cold pain threshold, tolerance, intensity and unpleasantness
1, 2, 3, 4, 5, 6, 8, 10, 12 hours after the administration of buprenorphine

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart

1 april 2013

Primärt slutförande (Faktisk)

1 november 2014

Avslutad studie (Faktisk)

1 november 2014

Studieregistreringsdatum

Först inskickad

27 april 2013

Först inskickad som uppfyllde QC-kriterierna

12 maj 2013

Första postat (Uppskatta)

15 maj 2013

Uppdateringar av studier

Senaste uppdatering publicerad (Uppskatta)

20 november 2014

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

19 november 2014

Senast verifierad

1 november 2014

Mer information

Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .

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