- ICH GCP
- Yhdysvaltain kliinisten tutkimusten rekisteri
- Kliininen tutkimus NCT02715700
Effects of Doravirine (MK-1439) on Methadone Pharmacokinetics in Methadone-Maintained Participants (MK-1439-045)
keskiviikko 12. kesäkuuta 2019 päivittänyt: 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.
Tutkimuksen yleiskatsaus
Tila
Valmis
Interventio / Hoito
Opintotyyppi
Interventio
Ilmoittautuminen (Todellinen)
14
Vaihe
- Vaihe 1
Osallistumiskriteerit
Tutkijat etsivät ihmisiä, jotka sopivat tiettyyn kuvaukseen, jota kutsutaan kelpoisuuskriteereiksi. Joitakin esimerkkejä näistä kriteereistä ovat henkilön yleinen terveydentila tai aiemmat hoidot.
Kelpoisuusvaatimukset
Opintokelpoiset iät
18 vuotta - 65 vuotta (Aikuinen, Vanhempi Aikuinen)
Hyväksyy terveitä vapaaehtoisia
Joo
Sukupuolet, jotka voivat opiskella
Kaikki
Kuvaus
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.
Opintosuunnitelma
Tässä osiossa on tietoja tutkimussuunnitelmasta, mukaan lukien kuinka tutkimus on suunniteltu ja mitä tutkimuksella mitataan.
Miten tutkimus on suunniteltu?
Suunnittelun yksityiskohdat
- Ensisijainen käyttötarkoitus: Hoito
- Jako: Ei käytössä
- Inventiomalli: Yksittäinen ryhmätehtävä
- Naamiointi: Ei mitään (avoin tarra)
Aseet ja interventiot
Osallistujaryhmä / Arm |
Interventio / Hoito |
|---|---|
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Kokeellinen: 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.
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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.
Muut nimet:
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Mitä tutkimuksessa mitataan?
Ensisijaiset tulostoimenpiteet
Tulosmittaus |
Toimenpiteen kuvaus |
Aikaikkuna |
|---|---|---|
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Area Under the Concentration-Time Curve From Zero to 24 Hours After Dosing (AUC0-24) of R-Methadone
Aikaikkuna: 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
|
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Plasma Concentration at 24 Hours After Dosing (C24) of R-Methadone
Aikaikkuna: 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
|
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Maximum Plasma Concentration (Cmax) of R-Methadone
Aikaikkuna: 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
Aikaikkuna: 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
Aikaikkuna: 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
Aikaikkuna: 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
Aikaikkuna: 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
Aikaikkuna: 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
Aikaikkuna: 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
Aikaikkuna: 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
Aikaikkuna: 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
Aikaikkuna: 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
|
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Opintojen ennätyspäivät
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Opi tärkeimmät päivämäärät
Opiskelun aloitus (Todellinen)
Maanantai 28. syyskuuta 2015
Ensisijainen valmistuminen (Todellinen)
Maanantai 13. kesäkuuta 2016
Opintojen valmistuminen (Todellinen)
Maanantai 15. elokuuta 2016
Opintoihin ilmoittautumispäivät
Ensimmäinen lähetetty
Torstai 17. maaliskuuta 2016
Ensimmäinen toimitettu, joka täytti QC-kriteerit
Maanantai 21. maaliskuuta 2016
Ensimmäinen Lähetetty (Arvio)
Tiistai 22. maaliskuuta 2016
Tutkimustietojen päivitykset
Viimeisin päivitys julkaistu (Todellinen)
Tiistai 25. kesäkuuta 2019
Viimeisin lähetetty päivitys, joka täytti QC-kriteerit
Keskiviikko 12. kesäkuuta 2019
Viimeksi vahvistettu
Lauantai 1. kesäkuuta 2019
Lisää tietoa
Tähän tutkimukseen liittyvät termit
Muita asiaankuuluvia MeSH-ehtoja
- RNA-virusinfektiot
- Virussairaudet
- Infektiot
- Veren välityksellä leviävät infektiot
- Tartuntataudit
- Sukupuolitaudit, virus
- Sukupuolitaudit
- Lentivirus-infektiot
- Retroviridae-infektiot
- Immunologiset puutosoireyhtymät
- Immuunijärjestelmän sairaudet
- Hitaat virustaudit
- HIV-infektiot
- Immuunikato
- Huumeiden fysiologiset vaikutukset
- Keskushermostoa lamaavat aineet
- Ääreishermoston aineet
- Analgeetit
- Aistijärjestelmän agentit
- Analgeetit, opioidit
- Huumausaineet
- Hengityselinten aineet
- Yskänlääkkeitä
- Metadoni
Muut tutkimustunnusnumerot
- 1439-045
- MK-1439-045 (Muu tunniste: Merck Protocol Number)
Yksittäisten osallistujien tietojen suunnitelma (IPD)
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JOO
IPD-suunnitelman kuvaus
http://engagezone.msd.com/doc/ProcedureAccessClinicalTrialData.pdf
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