- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT02245451
Study of Tipranavir and Ritonavir on the Pharmacokinetic Characteristics of Methadone Administered in Healthy Volunteers
18 september 2014 uppdaterad av: Boehringer Ingelheim
A Single-centre, Open-label Study of Multiple Doses of Tipranavir 500 mg and Ritonavir 200 mg (Twice Daily) on the Pharmacokinetic Characteristics of Methadone Administered as a Single Dose in Healthy Volunteers
The primary objective of this study is to characterise the effects of tipranavir 500 mg and ritonavir 200 mg (TPV/r; given twice daily) at steady-state on the pharmacokinetics of methadone administered as a single dose in healthy adult volunteers
Studieöversikt
Status
Avslutad
Betingelser
Intervention / Behandling
Studietyp
Interventionell
Inskrivning (Faktisk)
15
Fas
- Fas 1
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 60 år (Vuxen)
Tar emot friska volontärer
Ja
Kön som är behöriga för studier
Allt
Beskrivning
Inclusion Criteria:
- Male or female healthy volunteers aged at least 18 to 60 years.
- Clinically normal medical history.
- Clinically normal findings on physical examination.
- Clinically normal laboratory values.
- A Body Mass Index >18.5 and <30 kg/m2.
- Able to swallow large capsules without difficulty.
- Capable of comprehending and communicating effectively with the investigator and staff and of providing written informed consent in accordance with ethics committee and regulatory guidelines.
- Willing to stay in the study centre for the duration of the study.
- Willing to abstain from ingesting substances during the study which may alter plasma study drug levels by interaction with the cytochrome P450 system.
- Willing to abstain from alcohol for 48 hours prior to Visit 1 and for the duration of the study. In addition, Cabernet Sauvignon must not have been ingested within 15 days prior to Visit 1.
- Willing to abstain from ingesting grapefruit and grapefruit juice for 15 days before Visit 1 and for the duration of the study.
- Willing to abstain from ingesting Seville oranges, strawberries or strawberry extract, garlic supplements, St. John's Wort, Milk Thistle, or methylxanthine-containing drinks or food (coffee, tea, cola, energy drinks, chocolate, etc) for 72 hours before the pharmacokinetic sampling days.
- Willing to abstain from use of tobacco products for the duration of the study.
- Urine drug screen negative for illegal non-prescription drugs.
- Negative HIV serology.
- Negative for Hepatitis B surface antigen and Hepatitis C
Exclusion Criteria:
- Any clinically significant disease. (A significant disease was defined as a disease which in the opinion of the investigator may either have put the subject at risk because of participation in the study or a disease which may have influenced the results of the study or the subject's ability to participate in the study.)
- Clinically significant abnormal baseline haematology, blood chemistry or urinalysis findings.
- Serum alanine aminotransferase (ALT), aspartate aminotransferase (AST), cholesterol, triglyceride or glucose greater than the upper limit of normal at Visit 1.
- Treatment with prohibited medications in the thirty days before the study or during the study or ingestion of drugs of abuse.
- Treatment with any investigational drug within 90 days of the first dose of study medication.
- Inability to adhere to the requirements of the protocol (including active substance abuse) as assessed by the investigator.
- Prior tipranavir use.
- Ingestion of any known enzyme altering drug (such as phenothiazines, cimetidine, barbiturates, ketoconazole, fluconazole, clarithromycin, rifampin, steroids, and herbal medications) for thirty days prior to Visit 1.
- Ingestion of grapefruit, grapefruit juice, and Cabernet Sauvignon within fifteen days prior to Visit 1.
- Ingestion of Seville oranges, strawberries or strawberry extract, garlic supplements, St. John's Wort, Milk Thistle, or methylxanthine-containing drinks or food (coffee, tea, cola, energy drinks, chocolate, etc) within 72 hours of pharmacokinetics sampling days.
- Treatment with prescription medicines within thirty days prior to Visit 1.
- History of gastrointestinal, hepatic, or renal disorders within 60 days prior to Visit 1.
- Any history of alcohol or drug abuse.
- Current use of cigarettes defined as greater than 10 cigarettes per day or rolling/pipe tobacco equivalent.
- Blood or plasma donations within 90 days prior to Visit 1
- Subjects with a seated systolic blood pressure either <100 mm Hg or >150 mm Hg; resting heart rate either <50 beats/min or >100 beats/min.
- Subjects with a history of any illness or allergy that, in the opinion of the investigator, might have confounded the results of the study or posed additional risk in administering tipranavir, ritonavir or methadone to the subject.
- Subjects who had an acute illness within two weeks prior to Visit 1.
- Subjects who were currently taking any over-the-counter drug within fourteen days prior to Visit 1 or who were currently taking any prescription drug.
- Hypersensitivity to tipranavir, ritonavir, or methadone.
- Female subjects who are of reproductive potential and who were pregnant, breastfeeding, had a positive serum B-HCG at Visit 1 or 2, had not been using a barrier contraceptive method for at least three months prior to Study Day 1 or were not willing to use a reliable method of double-barrier contraception (such as diaphragm with spermicidal cream/jelly or condoms with spermicidal foam) during the study and for thirty days after completion or termination of the study.
Studieplan
Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Behandling
- Tilldelning: Icke-randomiserad
- Interventionsmodell: Enskild gruppuppgift
- Maskning: Ingen (Open Label)
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
|
Experimentell: TPV/r with methadone
|
Vad mäter studien?
Primära resultatmått
Resultatmått |
Tidsram |
|---|---|
|
Area under the concentration-time curve for 0 to 24 hours (AUC0-24h) of methadone
Tidsram: up to 24 hours after drug administration
|
up to 24 hours after drug administration
|
|
Maximum concentration (Cmax)
Tidsram: up to 24 hours after drug administration
|
up to 24 hours after drug administration
|
|
Concentration at 6 hours (C6h) of methadone
Tidsram: 6 hours after drug administration
|
6 hours after drug administration
|
|
Area under the concentration-time curve for 0 to 12 hours (AUC0-12h) of tipranavir and ritonavir
Tidsram: up to 12 hours after drug administration
|
up to 12 hours after drug administration
|
|
concentration at 12 hours (C12h) of tipranavir and ritonavir
Tidsram: 12 hours after drug administration
|
12 hours after drug administration
|
Sekundära resultatmått
Resultatmått |
Tidsram |
|---|---|
|
mean residence time (MRT)
Tidsram: up to 24 hours after drug administration
|
up to 24 hours after drug administration
|
|
apparent terminal half-life (t½)
Tidsram: up to 24 hours after drug administration
|
up to 24 hours after drug administration
|
|
time to maximum concentration (Tmax)
Tidsram: up to 24 hours after drug administration
|
up to 24 hours after drug administration
|
|
oral clearance (CL/F)
Tidsram: up to 24 hours after drug administration
|
up to 24 hours after drug administration
|
|
apparent volume of distribution during the terminal elimination phase divided by the bioavailability factor (Vz/F)
Tidsram: up to 24 hours after drug administration
|
up to 24 hours after drug administration
|
|
Number of patients with abnormal findings in physical examination
Tidsram: Up to day 17 after first drug administration
|
Up to day 17 after first drug administration
|
|
Number of patients with clinically significant changes in vital signs
Tidsram: Up to day 17 after first drug administration
|
Up to day 17 after first drug administration
|
|
Number of patients with abnormal changes in clinical laboratory parameters
Tidsram: Up to day 17 after first drug administration
|
Up to day 17 after first drug administration
|
|
Number of participants with adverse events
Tidsram: Up to day 17 after first drug administration
|
Up to day 17 after first drug administration
|
Samarbetspartners och utredare
Det är här du hittar personer och organisationer som är involverade i denna studie.
Sponsor
Publikationer och användbara länkar
Den som ansvarar för att lägga in information om studien tillhandahåller frivilligt dessa publikationer. Dessa kan handla om allt som har med studien att göra.
Användbara länkar
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 januari 2005
Primärt slutförande (Faktisk)
1 februari 2005
Studieregistreringsdatum
Först inskickad
18 september 2014
Först inskickad som uppfyllde QC-kriterierna
18 september 2014
Första postat (Uppskatta)
19 september 2014
Uppdateringar av studier
Senaste uppdatering publicerad (Uppskatta)
19 september 2014
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
18 september 2014
Senast verifierad
1 september 2014
Mer information
Termer relaterade till denna studie
Ytterligare relevanta MeSH-villkor
- Läkemedels fysiologiska effekter
- Molekylära mekanismer för farmakologisk verkan
- Anti-infektionsmedel
- Depressiva medel i centrala nervsystemet
- Agenter från det perifera nervsystemet
- Antivirala medel
- Enzyminhibitorer
- Anti-HIV-medel
- Antiretrovirala medel
- Analgetika
- Sensoriska systemagenter
- Proteashämmare
- Analgetika, Opioid
- Narkotika
- Cytokrom P-450 CYP3A-hämmare
- Cytokrom P-450 enzymhämmare
- Andningsorgan
- HIV-proteashämmare
- Virala proteashämmare
- Hostdämpande medel
- Ritonavir
- Tipranavir
- Metadon
Andra studie-ID-nummer
- 1182.26
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 .