Once-daily Highly Active Antiretroviral Treatment Regimen Administration in HIV-1 Infected Children in Burkina Faso (ANRS 12103 BURKINAME)

French National Agency for Research on AIDS and Viral Hepatitis

Status and phase

Completed

Phase 2

Conditions

AIDS

HIV Infections

Treatments

Drug: Didanosine (ddI)

Drug: Lamivudine (3TC)

Drug: Efavirenz (EFV)

Study type

Interventional

Funder types

Other

Identifiers

NCT00122538

ANRS 12103 BURKINAME

Details and patient eligibility

About

The purpose of this study is to try a known antiretroviral combination in HIV- infected children with only one intake a day, in order to simplify the prescription and improve adherence to treatment. This is what is called a phase II clinical trial, only recruiting and following a small number of children (50) during one year to evaluate the quantity of drug in the blood just before it is taken and one to three hours after it is taken. The other important objective is to study the tolerance of drugs in that mode of prescription of the triple combination.

Full description

The data relating to pharmacology tolerance and efficacy of the once-daily combination of 3TC + ddI + EFV have never been studied.

This regimen may lead to a better treatment of the HIV-1 infected children in developing countries, as well as in Europe. Because of its simplicity it would facilitate observance that is one of the essential parameters of efficacy of treatments.

The main objectives are those of a phase II clinical trial:

Assess the virological and immunological efficacy of a once daily HAART regimen comprising lamivudine (3TC) + didanosine (ddI) + efavirenz (EFV) [pediatric reference];
Analyse the pharmacological characteristics of this combination in children;
Assess the tolerance;
Study the appearance of resistance;
Evaluate the observance to treatment.

50 HIV-1 infected children aged 30 months to 15 years whose clinical and immunological state (stage B or C) requires antiretroviral treatment, will be included in the study. They should be naive of any ARV treatment (except the treatment received in the framework of PMTCT (Prevention of Mother to Child Transmission).

Data Collection and Development of the Study:

Monthly clinical examination;
RNA HIV-1 and CD4 counts;
Pharmacological dosages;
Haematology and biochemistry surveillance;
Genotypic resistance at inclusion; and, in case of unsuccess or failure,
Assessment of observance according to alternate methods.

Laboratory examinations will be carried out at Centre Muraz except for genotyping and for pharmacological tests sent to Montpellier Teaching Hospital (France).

Enrollment

52 patients

Sex

All

Ages

30 months to 15 years old

Volunteers

No Healthy Volunteers

Inclusion criteria