Cocktail Approach for Cytochrome P450 and P-glycoprotein Activity Assessment Using Dried Blood Spot
1 other identifier
interventional
10
1 country
1
Brief Summary
Phenotyping is an approach largely used for the evaluation of the activity of cytochromes and transporters in vivo. It consists of the administration of probe substances metabolised by a specific cytochrome or transported by P-glycoprotein (P-gp) for example, followed by the determination of a metabolic ratio or the evaluation of the plasmatic or urinary concentrations of the probe substances. The administration of a cocktail containing several probe substances allows the simultaneous evaluation of the activity of several cytochromes and P-gp in a single test. The aim of this project is the validation of a phenotyping cocktail of low dose probe drugs for the assessment of cytochrome P450 and P-gp activities by simple capillary blood sampling and dried blood spot (DBS) analysis. The cocktail consists of caffeine, bupropion, flurbiprofen, omeprazole, dextromethorphan, midazolam and fexofenadine for the simultaneous phenotyping of CYP1A2, CYP2B6, CYP2C9, CAP2C19, CYP2D6, CYP3A4 and P-gp, respectively. The modulation of the activity of cytochromes or P-gp will be evaluated by the administration of inhibitors (fluvoxamine, voriconazole, quinidine) or inducer (rifampicin) of the metabolic pathways or the P-gp mediated transport.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for phase_1 healthy-volunteers
Started Nov 2012
Longer than P75 for phase_1 healthy-volunteers
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 1, 2012
CompletedFirst Submitted
Initial submission to the registry
November 14, 2012
CompletedFirst Posted
Study publicly available on registry
November 21, 2012
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 1, 2013
CompletedStudy Completion
Last participant's last visit for all outcomes
January 1, 2014
CompletedSeptember 16, 2014
September 1, 2014
6 months
November 14, 2012
September 15, 2014
Conditions
Outcome Measures
Primary Outcomes (1)
Probe cocktail drugs plasma and capillary concentrations in presence/absence of CYP1A2,2B6, 2C9, 2C19, 2D6, 3A4 and P-gp inhibitor or inducer
4 singles days spaced out with one week wash-out periods
Secondary Outcomes (2)
correlation between plasma or urine and capillary concentrations for each probe cocktail drug
4 singles days spaced out with one week wash-out periods
comparison. between genotype and phenotype for each enzyme
one day
Study Arms (4)
CYP1A2, 2B6, 2C9, 2C19, 3A4 inhibitors
ACTIVE COMPARATOROral intake of fluvoxamine (50 mg per day during 2 days) and voriconazole (400 mg) before oral intake of the cocktail probe drugs
CYP2D6 and P-gp inhibitor
ACTIVE COMPARATOROral intake of quinidine (200 mg) before oral intake of the cocktail probe drugs
CYPs and P-gp inducer
ACTIVE COMPARATOROral intake of rifampicin (600 mg per day during 7 days) before oral intake of the cocktail probe drugs
Probe cocktail alone
EXPERIMENTALOral intake of the cocktail probe drugs : * bupropion 25 mg * flurbiprofen 25 mg * omeprazole 5 mg * dextromethorphan 5 mg * midazolam 1 mg * fexofenadine 25mg * Caffeine (a cup of coffee)
Interventions
Eligibility Criteria
You may qualify if:
- Healthy male volunteers aged from 18 to 60 years
- BMI between 18 and 25
- Understanding of French language and able to give a written inform consent.
You may not qualify if:
- Smoker
- Taking drugs which alter CYPs activity
- Renal or hepatic impairment
- Medical history of porphyria
- Medical history of chronic alcoholism or abuse of psychoactive drugs
- Liver transplantation
- Sensitivity to any of the drugs used
- Wearing contact lenses (risk of coloration with rifampicin)
- ECG showing long QT interval (\>0.46sec)
- Alteration of hepatic tests
- Presenting genetic polymorphism of poor CYP 2B6, 2C9, 2C19, 2D6 metabolisers
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Jules Desmeuleslead
Study Sites (1)
University Hospitals
Geneva, Switzerland
Related Publications (1)
Bosilkovska M, Samer CF, Deglon J, Rebsamen M, Staub C, Dayer P, Walder B, Desmeules JA, Daali Y. Geneva cocktail for cytochrome p450 and P-glycoprotein activity assessment using dried blood spots. Clin Pharmacol Ther. 2014 Sep;96(3):349-59. doi: 10.1038/clpt.2014.83. Epub 2014 Apr 10.
PMID: 24722393DERIVED
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Jules A Desmeules, Pr
University Hospital, Geneva
Study Design
- Study Type
- interventional
- Phase
- phase 1
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Purpose
- DIAGNOSTIC
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Pr
Study Record Dates
First Submitted
November 14, 2012
First Posted
November 21, 2012
Study Start
November 1, 2012
Primary Completion
May 1, 2013
Study Completion
January 1, 2014
Last Updated
September 16, 2014
Record last verified: 2014-09