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

19 novembre 2014 mis à jour par: 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.

Aperçu de l'étude

Description détaillée

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.

Type d'étude

Interventionnel

Inscription (Réel)

12

Phase

  • Phase 4

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Lieux d'étude

      • Turku, Finlande, 20500
        • Turku University Hospital

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

18 ans à 40 ans (Adulte)

Accepte les volontaires sains

Oui

Sexes éligibles pour l'étude

Tout

La description

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.

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Science basique
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation croisée
  • Masquage: Seul

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Comparateur actif: 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
Comparateur placebo: 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 ]
Comparateur actif: 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.
Autres noms:
  • Temgesic 0,2 mg resoriblet
  • Temgesic 0,3 mg/ml

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Délai
Concentration of buprenorphine and its metabolites in plasma and urine concebtration of buprenorphine
Délai: 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

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Pharmacodynamic effects
Délai: 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
Délai: 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

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude

1 avril 2013

Achèvement primaire (Réel)

1 novembre 2014

Achèvement de l'étude (Réel)

1 novembre 2014

Dates d'inscription aux études

Première soumission

27 avril 2013

Première soumission répondant aux critères de contrôle qualité

12 mai 2013

Première publication (Estimation)

15 mai 2013

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Estimation)

20 novembre 2014

Dernière mise à jour soumise répondant aux critères de contrôle qualité

19 novembre 2014

Dernière vérification

1 novembre 2014

Plus d'information

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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