NCT01731067

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
10

participants targeted

Target at below P25 for phase_1 healthy-volunteers

Timeline
Completed

Started Nov 2012

Longer than P75 for phase_1 healthy-volunteers

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

November 1, 2012

Completed
13 days until next milestone

First Submitted

Initial submission to the registry

November 14, 2012

Completed
7 days until next milestone

First Posted

Study publicly available on registry

November 21, 2012

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2013

Completed
8 months until next milestone

Study Completion

Last participant's last visit for all outcomes

January 1, 2014

Completed
Last Updated

September 16, 2014

Status Verified

September 1, 2014

Enrollment Period

6 months

First QC Date

November 14, 2012

Last Update Submit

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 COMPARATOR

Oral intake of fluvoxamine (50 mg per day during 2 days) and voriconazole (400 mg) before oral intake of the cocktail probe drugs

Drug: Cocktail probe drugs

CYP2D6 and P-gp inhibitor

ACTIVE COMPARATOR

Oral intake of quinidine (200 mg) before oral intake of the cocktail probe drugs

Drug: Cocktail probe drugs

CYPs and P-gp inducer

ACTIVE COMPARATOR

Oral intake of rifampicin (600 mg per day during 7 days) before oral intake of the cocktail probe drugs

Drug: Cocktail probe drugs

Probe cocktail alone

EXPERIMENTAL

Oral 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)

Drug: Cocktail probe drugs

Interventions

Also known as: Oral 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)
CYP1A2, 2B6, 2C9, 2C19, 3A4 inhibitorsCYP2D6 and P-gp inhibitorCYPs and P-gp inducerProbe cocktail alone

Eligibility Criteria

Age18 Years - 65 Years
Sexmale
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

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

Study Sites (1)

University Hospitals

Geneva, Switzerland

Location

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.

MeSH Terms

Interventions

BupropionFlurbiprofenOmeprazoleDextromethorphanMidazolamfexofenadineCaffeine

Intervention Hierarchy (Ancestors)

PropiophenonesKetonesOrganic ChemicalsPropionatesAcids, AcyclicCarboxylic AcidsBiphenyl CompoundsBenzene DerivativesHydrocarbons, AromaticHydrocarbons, CyclicHydrocarbons2-PyridinylmethylsulfinylbenzimidazolesSulfoxidesSulfur CompoundsPyridinesHeterocyclic Compounds, 1-RingHeterocyclic CompoundsBenzimidazolesHeterocyclic Compounds, 2-RingHeterocyclic Compounds, Fused-RingMorphinansOpiate AlkaloidsAlkaloidsHeterocyclic Compounds, Bridged-RingHeterocyclic Compounds, 4 or More RingsPhenanthrenesPolycyclic Aromatic HydrocarbonsPolycyclic CompoundsBenzodiazepinesBenzazepinesXanthinesPurinonesPurines

Study Officials

  • Jules A Desmeules, Pr

    University Hospital, Geneva

    PRINCIPAL INVESTIGATOR

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

Locations