Clinical Trials Directory

Trials / Completed

CompletedNCT01344512

Population Pharmacokinetics of Anti-infectious Drugs in Children

Population Pharmacokinetics Of Ceftazidime, Ciprofloxacin And Voriconazole In Paediatric Young Patients (< 12 Years Old)

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
214 (actual)
Sponsor
University Hospital, Bordeaux · Academic / Other
Sex
All
Age
28 Days – 6 Years
Healthy volunteers
Not accepted

Summary

The Pharm A project is a French national collaborative project aiming to determine the population pharmacokinetics of ceftazidime, ciprofloxacin, and voriconazole in paediatric patients aged one month to five years.

Detailed description

The licensing process was introduced in order to ensure that medicines are safe, effective and of high quality. However, over 50% of children admitted to hospital in France and Europe will receive an unlicensed or off-label medicine. This occurs for most drugs in children less than 6 years of age. They represent a particularly vulnerable subgroup of the paediatric population. There are major practical and ethical issues in relation to studying medicines in paediatric patients aged 5 years or less. * They represent only a small part of the population as compared to older children and adults, and the variation of specific types of diseases in this young subpopulation is higher than in the paediatric counterpart. There are major differences in drug disposition in the different age groups. * There is a need for suitable methodological approaches for clinical trials * There are major ethical issues It is essential, therefore, to recruit children from various regions in France in order to obtain a critical sample size of sufficient magnitude and to conduct scientific sound studies. This will be achieved by performing Pharm A, a population pharmacokinetic study of three different anti infectious agents (ceftazidime, ciprofloxacin, voriconazole) and identify covariates including pharmacogenetic biomarkers that explain pharmacokinetic variability. After parental informed consent, sampling strategy will be randomized depending on the drug and the age group (2 samples in patients below 2 years and 3 samples in patients from 2 to 5 years).

Conditions

Interventions

TypeNameDescription
DRUGCeftazidimeBloods sampling on patient treated with Ceftazidime between 48 hours and 4 days after beginning of treatment.
DRUGCiprofloxacinBloods sampling on patient treated with Ciprofloxacin between 48 hours and 4 days after beginning of treatment.
DRUGVoriconazoleBloods sampling on patient treated with Voriconazole between 48 hours and 4 days after beginning of treatment.

Timeline

Start date
2011-06-01
Primary completion
2014-09-01
Completion
2014-09-01
First posted
2011-04-29
Last updated
2015-03-18

Locations

14 sites across 1 country: France

Source: ClinicalTrials.gov record NCT01344512. Inclusion in this directory is not an endorsement.