- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT02715700
Effects of Doravirine (MK-1439) on Methadone Pharmacokinetics in Methadone-Maintained Participants (MK-1439-045)
12 juin 2019 mis à jour par: Merck Sharp & Dohme LLC
A Multiple-Dose Clinical Trial to Study the Effect of MK-1439 (Doravirine) on Methadone Pharmacokinetics
This study will evaluate the effects of multiple doses of doravirine (MK-1439) on the pharmacokinetics of methadone in participants requiring methadone maintenance therapy.
The primary hypothesis is that area under the plasma concentration-time curve to 24 hours postdose (AUC0-24) of (R)-methadone is similar when a maintenance regimen of methadone is administered with or without multiple daily doses of doravirine.
Aperçu de l'étude
Statut
Complété
Les conditions
Intervention / Traitement
Type d'étude
Interventionnel
Inscription (Réel)
14
Phase
- La phase 1
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 65 ans (Adulte, Adulte plus âgé)
Accepte les volontaires sains
Oui
Sexes éligibles pour l'étude
Tout
La description
Inclusion Criteria:
- If female with reproductive potential: must demonstrate a serum β-human chorionic gonadotropin (β -hCG) level consistent with the nongravid state and agree to use (and/or have their partner use) two acceptable methods of birth control throughout the trial and until 2 weeks after the last dose of trial drug.
- If postmenopausal female: must be without menses for at least 1 year.
- If surgically sterile female: must have a status of post hysterectomy, oophorectomy or tubal ligation.
- Body Mass Index (BMI) of 18-35 kg/m^2 (inclusive).
- Able to comply with the smoking restrictions, including <=10 cigarettes per day while in the Clinical Research Unit, and no smoking from 2 hours predose to 2 hours postdose on Days 1 and 6.
- Reliably participating in a methadone maintenance program for at least two months prior to Day 1. Required to be on a documented stable dose of methadone for at least 14 days prior to Day 1.
- Agree not to change current maintenance methadone dose of 20-200 mg once daily (unless for safety reasons) from screening until the end of the study. Must agree to observation and documentation of daily methadone dose administration during the period of the study during which they are domiciled.
Exclusion Criteria:
- Mentally or legally incapacitated, have significant emotional problems at the time of pretrial (screening) visit or expected during the conduct of the trial or have a history of clinically significant psychiatric disorder of the last 5 years. Participants who have had situational depression may be enrolled in the trial at the discretion of the investigator.
- History of clinically significant endocrine, gastrointestinal, cardiovascular, hematological, hepatic, immunological, renal, respiratory, genitourinary or major neurological (including stroke and chronic seizures) abnormalities or diseases. Participants with a history of uncomplicated kidney stones or childhood asthma may be enrolled in the trial at the discretion of the investigator.
- History of cancer (malignancy) - exceptions apply.
- History of significant multiple and/or severe allergies (e.g. food, drug, latex allergy), or has had an anaphylactic reaction or significant intolerability to prescription or non-prescription drugs or food.
- Positive for Human Immunodeficiency Virus (HIV).
- Major surgery, donated or lost 1 unit of blood (approximately 500 mL) within 4 weeks prior to the pretrial (screening) visit.
- Participated in another investigational trial within 4 weeks prior to the pretrial (screening) visit.
- Nursing mother.
- Unable to refrain from or anticipates the use of any medication, including prescription and non-prescription drugs or herbal remedies beginning approximately 2 weeks prior to the first dose of the 14 day methadone maintenance phase prior to Day 1, throughout the trial, until the post-trial visit - exceptions apply.
- Consumes greater than 3 glasses of alcoholic beverages (1 glass is approximately equivalent to: beer [354 mL/12 ounces], wine [118 mL/4 ounces], or distilled spirits [29.5 mL/1 ounce]) per day - exceptions apply.
- Consumes excessive amounts of caffeine, defined as greater than 6 servings (1 serving is approximately equivalent to 120 mg of caffeine) of coffee, tea, cola, energy-drinks, or other caffeinated beverages per day.
- Has a positive screen for drugs with a high potential for abuse such as cocaine, amphetamines, methylenedioxymethamphetamine (MDMA), barbiturates, benzodiazepines (exceptions apply), or opiates/opioids (apart from methadone as assigned maintenance therapy) on Day 1 that cannot be explained by concomitant medications, unless at the discretion of the principal investigator and the sponsor. Must have a negative Urine Drug Screen prior to randomization, with the exception of tetrahydrocannabinol (THC) and prescription benzodiazepines.
- Clinical Opiate Withdrawal Scale (COWS) score of >=5 prior to randomization.
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: Traitement
- Répartition: N / A
- Modèle interventionnel: Affectation à un seul groupe
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: Maintenance Methadone and MK-1439
Participants maintained on a stable methadone regimen (20 to 200 mg once daily) for ≥14 days prior to Day 1 will continue to receive methadone maintenance once per day on Days 1 to 7. From Day 2 to 6, participants will also receive doravirine 100 mg once daily.
|
Methadone 20 to 200 mg (10 mg/mL if oral solution concentrate) oral tablet once per day.
Doravirine 100 mg oral tablet once per day.
Autres noms:
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Area Under the Concentration-Time Curve From Zero to 24 Hours After Dosing (AUC0-24) of R-Methadone
Délai: Predose and 0.5, 1, 1.5, 2, 3, 4, 6, 12, 16, and 24 hours postdose on Day 1 and Day 6
|
The AUC0-24 of the R- methadone enantiomer was determined on Day 1 (methadone alone) and on Day 6 (methadone + doravirine).
Plasma samples collected for methadone assay were analyzed for R- and S-methadone concentrations by Pharma Medica Research Inc. (Ontario, Canada).
The analytical method used liquid-liquid extraction for analyte isolation followed by liquid chromatographic-tandem mass spectrometric (LC-MS/MS) detection.
The lower limit of quantification (LLoQ) was 0.0250 ng/mL for each enantiomer.
The analytical range was 0.0250 - 15.0 ng/mL.
|
Predose and 0.5, 1, 1.5, 2, 3, 4, 6, 12, 16, and 24 hours postdose on Day 1 and Day 6
|
|
Plasma Concentration at 24 Hours After Dosing (C24) of R-Methadone
Délai: 24 hours postdose on Day 1 and Day 6
|
The C24 of the R- methadone enantiomer was determined on Day 1 (methadone alone) and on Day 6 (methadone + doravirine).
Plasma samples collected for methadone assay were analyzed for R- and S-methadone concentrations by Pharma Medica Research Inc. (Ontario, Canada).
The analytical method used liquid-liquid extraction for analyte isolation followed by LC-MS/MS detection.
The LLoQ was 0.0250 ng/mL for each enantiomer.
The analytical range was 0.0250 - 15.0 ng/mL.
|
24 hours postdose on Day 1 and Day 6
|
|
Maximum Plasma Concentration (Cmax) of R-Methadone
Délai: Predose and 0.5, 1, 1.5, 2, 3, 4, 6, 12, 16, and 24 hours postdose on Day 1 and Day 6
|
The Cmax of the R- methadone enantiomer was determined on Day 1 (methadone alone) and on Day 6 (methadone + doravirine).
Plasma samples collected for methadone assay were analyzed for R- and S-methadone concentrations by Pharma Medica Research Inc. (Ontario, Canada).
The analytical method used liquid-liquid extraction for analyte isolation followed by LC-MS/MS detection.
The LLoQ was 0.0250 ng/mL for each enantiomer.
The analytical range was 0.0250 - 15.0 ng/mL.
|
Predose and 0.5, 1, 1.5, 2, 3, 4, 6, 12, 16, and 24 hours postdose on Day 1 and Day 6
|
|
Time to Maximum Plasma Concentration (Tmax) of R-Methadone
Délai: Predose and 0.5, 1, 1.5, 2, 3, 4, 6, 12, 16, and 24 hours postdose on Day 1 and Day 6
|
The Tmax of the R- methadone enantiomer was determined on Day 1 (methadone alone) and on Day 6 (methadone + doravirine).
Plasma samples collected for methadone assay were analyzed for R- and S-methadone concentrations by Pharma Medica Research Inc. (Ontario, Canada).
The analytical method used liquid-liquid extraction for analyte isolation followed by LC-MS/MS detection.
The LLoQ was 0.0250 ng/mL for each enantiomer.
The analytical range was 0.0250 - 15.0 ng/mL.
|
Predose and 0.5, 1, 1.5, 2, 3, 4, 6, 12, 16, and 24 hours postdose on Day 1 and Day 6
|
|
AUC0-24 of S-Methadone
Délai: Predose and 0.5, 1, 1.5, 2, 3, 4, 6, 12, 16, and 24 hours postdose on Day 1 and Day 6
|
The AUC0-24 of the S- methadone enantiomer was determined on Day 1 (methadone alone) and on Day 6 (methadone + doravirine).
Plasma samples collected for methadone assay were analyzed for R- and S-methadone concentrations by Pharma Medica Research Inc. (Ontario, Canada).
The analytical method used liquid-liquid extraction for analyte isolation followed by LC-MS/MS detection.
The LLoQ was 0.0250 ng/mL for each enantiomer.
The analytical range was 0.0250 - 15.0 ng/mL.
|
Predose and 0.5, 1, 1.5, 2, 3, 4, 6, 12, 16, and 24 hours postdose on Day 1 and Day 6
|
|
C24 of S-Methadone
Délai: 24 hours postdose on Day 1 and Day 6
|
The C24 of the S- methadone enantiomer was determined on Day 1 (methadone alone) and on Day 6 (methadone + doravirine).
Plasma samples collected for methadone assay were analyzed for R- and S-methadone concentrations by Pharma Medica Research Inc. (Ontario, Canada).
The analytical method used liquid-liquid extraction for analyte isolation followed by LC-MS/MS detection.
The LLoQ was 0.0250 ng/mL for each enantiomer.
The analytical range was 0.0250 - 15.0 ng/mL.
|
24 hours postdose on Day 1 and Day 6
|
|
Cmax of S-Methadone
Délai: Predose and 0.5, 1, 1.5, 2, 3, 4, 6, 12, 16, and 24 hours postdose on Day 1 and Day 6
|
The Cmax of the S- methadone enantiomer was determined on Day 1 (methadone alone) and on Day 6 (methadone + doravirine).
Plasma samples collected for methadone assay were analyzed for R- and S-methadone concentrations by Pharma Medica Research Inc. (Ontario, Canada).
The analytical method used liquid-liquid extraction for analyte isolation followed by LC-MS/MS detection.
The LLoQ was 0.0250 ng/mL for each enantiomer.
The analytical range was 0.0250 - 15.0 ng/mL.
|
Predose and 0.5, 1, 1.5, 2, 3, 4, 6, 12, 16, and 24 hours postdose on Day 1 and Day 6
|
|
Tmax of S-Methadone
Délai: Predose and 0.5, 1, 1.5, 2, 3, 4, 6, 12, 16, and 24 hours postdose on Day 1 and Day 6
|
The Tmax of the S- methadone enantiomer was determined on Day 1 (methadone alone) and on Day 6 (methadone + doravirine).
Plasma samples collected for methadone assay were analyzed for R- and S-methadone concentrations by Pharma Medica Research Inc. (Ontario, Canada).
The analytical method used liquid-liquid extraction for analyte isolation followed by LC-MS/MS detection.
The LLoQ was 0.0250 ng/mL for each enantiomer.
The analytical range was 0.0250 - 15.0 ng/mL.
|
Predose and 0.5, 1, 1.5, 2, 3, 4, 6, 12, 16, and 24 hours postdose on Day 1 and Day 6
|
|
AUC0-24 of Total Methadone
Délai: Predose and 0.5, 1, 1.5, 2, 3, 4, 6, 12, 16, and 24 hours postdose on Day 1 and Day 6
|
The AUC0-24 of total methadone was determined on Day 1 (methadone alone) and on Day 6 (methadone + doravirine).
Plasma samples collected for methadone assay were analyzed for R- and S-methadone concentrations by Pharma Medica Research Inc. (Ontario, Canada).
The analytical method used liquid-liquid extraction for analyte isolation followed by LC-MS/MS detection.
The LLoQ was 0.0250 ng/mL for each enantiomer.
The analytical range was 0.0250 - 15.0 ng/mL.
|
Predose and 0.5, 1, 1.5, 2, 3, 4, 6, 12, 16, and 24 hours postdose on Day 1 and Day 6
|
|
C24 of Total Methadone
Délai: 24 hours postdose on Day 1 and Day 6
|
The C24 of total methadone was determined on Day 1 (methadone alone) and on Day 6 (methadone + doravirine).
Plasma samples collected for methadone assay were analyzed for R- and S-methadone concentrations by Pharma Medica Research Inc. (Ontario, Canada).
The analytical method used liquid-liquid extraction for analyte isolation followed by LC-MS/MS detection.
The LLoQ was 0.0250 ng/mL for each enantiomer.
The analytical range was 0.0250 - 15.0 ng/mL.
|
24 hours postdose on Day 1 and Day 6
|
|
Cmax of Total Methadone
Délai: Predose and 0.5, 1, 1.5, 2, 3, 4, 6, 12, 16, and 24 hours postdose on Day 1 and Day 6
|
The Cmax of total methadone was determined on Day 1 (methadone alone) and on Day 6 (methadone + doravirine).
Plasma samples collected for methadone assay were analyzed for R- and S-methadone concentrations by Pharma Medica Research Inc. (Ontario, Canada).
The analytical method used liquid-liquid extraction for analyte isolation followed by LC-MS/MS detection.
The LLoQ was 0.0250 ng/mL for each enantiomer.
The analytical range was 0.0250 - 15.0 ng/mL.
|
Predose and 0.5, 1, 1.5, 2, 3, 4, 6, 12, 16, and 24 hours postdose on Day 1 and Day 6
|
|
Tmax of Total Methadone
Délai: Predose and 0.5, 1, 1.5, 2, 3, 4, 6, 12, 16, and 24 hours postdose on Day 1 and Day 6
|
The Tmax of total methadone was determined on Day 1 (methadone alone) and on Day 6 (methadone + doravirine).
Plasma samples collected for methadone assay were analyzed for R- and S-methadone concentrations by Pharma Medica Research Inc. (Ontario, Canada).
The analytical method used liquid-liquid extraction for analyte isolation followed by LC-MS/MS detection.
The LLoQ was 0.0250 ng/mL for each enantiomer.
The analytical range was 0.0250 - 15.0 ng/mL.
|
Predose and 0.5, 1, 1.5, 2, 3, 4, 6, 12, 16, and 24 hours postdose on Day 1 and Day 6
|
Collaborateurs et enquêteurs
C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.
Parrainer
Publications et liens utiles
La personne responsable de la saisie des informations sur l'étude fournit volontairement ces publications. Il peut s'agir de tout ce qui concerne l'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 (Réel)
28 septembre 2015
Achèvement primaire (Réel)
13 juin 2016
Achèvement de l'étude (Réel)
15 août 2016
Dates d'inscription aux études
Première soumission
17 mars 2016
Première soumission répondant aux critères de contrôle qualité
21 mars 2016
Première publication (Estimation)
22 mars 2016
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
25 juin 2019
Dernière mise à jour soumise répondant aux critères de contrôle qualité
12 juin 2019
Dernière vérification
1 juin 2019
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
- Infections par virus à ARN
- Maladies virales
- Infections
- Infections transmissibles par le sang
- Maladies transmissibles
- Maladies sexuellement transmissibles, virales
- Maladies sexuellement transmissibles
- Infections à lentivirus
- Infections à rétroviridae
- Syndromes d'immunodéficience
- Maladies du système immunitaire
- Maladies à virus lents
- Infections à VIH
- Syndrome immunodéficitaire acquis
- Effets physiologiques des médicaments
- Dépresseurs du système nerveux central
- Agents du système nerveux périphérique
- Analgésiques
- Agents du système sensoriel
- Analgésiques, Opioïdes
- Stupéfiants
- Agents du système respiratoire
- Agents antitussifs
- Méthadone
Autres numéros d'identification d'étude
- 1439-045
- MK-1439-045 (Autre identifiant: Merck Protocol Number)
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
OUI
Description du régime IPD
http://engagezone.msd.com/doc/ProcedureAccessClinicalTrialData.pdf
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