Once Daily Antiretroviral Therapy in HIV Infected Adults Treated With HAART
Primary Purpose
HIV Infections
Status
Completed
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
emtricitabine, FTC (drug)
didanosine, ddI (drug)
efavirenz (drug)
Sponsored by

About this trial
This is an interventional treatment trial for HIV Infections focused on measuring HIV Infections, Reverse Transcriptase Inhibitors, Treatment simplification
Eligibility Criteria
Inclusion Criteria: HIV infected adults Antiretroviral treatment since 6 months, with two nucleoside analogues and one or two protease inhibitors CD4 cell count over 100/mm3 HIV RNA below 400 copies/ml since 6 months Signed written informed consent Exclusion Criteria: Previous treatment with non nucleoside analogue, ddI alone Pregnancy Alcool abuse Acute infection, past neurological or pancreatic disease, biological abnormalities Chemotherapy or immunotherapy
Sites / Locations
Outcomes
Primary Outcome Measures
Virological success from W0 to W48
Secondary Outcome Measures
Progression of HIV infection
CD4 cell count
Safety
Treatment adherence
Quality of life
Viral mutations
Therapeutic strategy failure
Full Information
NCT ID
NCT00196612
First Posted
September 12, 2005
Last Updated
September 12, 2005
Sponsor
French National Agency for Research on AIDS and Viral Hepatitis
Collaborators
Triangle Pharmaceuticals, Gilead Sciences, Bristol-Myers Squibb, Dupont Applied Biosciences
1. Study Identification
Unique Protocol Identification Number
NCT00196612
Brief Title
Once Daily Antiretroviral Therapy in HIV Infected Adults Treated With HAART
Official Title
Phase II Randomized Trial Comparing Efficacy and Safety of the Maintenance of a HAART Association Protease Inhibitor Containing Versus a Once Daily Antiretroviral Triple Association, in HIV Adult Patients With Undetectable Viral Load.ANRS 099 ALIZE
Study Type
Interventional
2. Study Status
Record Verification Date
September 2005
Overall Recruitment Status
Completed
Study Start Date
April 2001 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
September 2004 (undefined)
3. Sponsor/Collaborators
Name of the Sponsor
French National Agency for Research on AIDS and Viral Hepatitis
Collaborators
Triangle Pharmaceuticals, Gilead Sciences, Bristol-Myers Squibb, Dupont Applied Biosciences
4. Oversight
5. Study Description
Brief Summary
The combination of two nucleoside analogues and one protease inhibitor is a highly active antiretroviral therapy (HAART) in HIV infected adults. In those with an undetectable viral load, a once daily combination of FTC, ddI, efavirenz would be easier to take, with less side effects and the same efficacy. The aim of the study was to evaluate if the once daily combination presents the same efficacy than the HAART therapy with less side effects and a better adherence.
Detailed Description
The combination of two nucleoside analogues and one protease inhibitor is a highly active antiretroviral therapy (HAART) in HIV infected adults, but side effects an the great number of pills induces less adherence to the therapy. Once daily combination with a lower number of pills could be more easy to take, with a greater adherence, less side effects, and the same efficacy. 355 patients are recruited in the study, randomized in two treatment groups: maintenance of the HAART therapy versus changing for a once daily combination of FTC, ddI, efavirenz, during 48 weeks. The primary end-point is the viral success maintained until 48 weeks. Secondary end-point is the safety and adherence.
The trial is prolonged for a total of 48 weeks.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infections
Keywords
HIV Infections, Reverse Transcriptase Inhibitors, Treatment simplification
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
350 (false)
8. Arms, Groups, and Interventions
Intervention Type
Drug
Intervention Name(s)
emtricitabine, FTC (drug)
Intervention Type
Drug
Intervention Name(s)
didanosine, ddI (drug)
Intervention Type
Drug
Intervention Name(s)
efavirenz (drug)
Primary Outcome Measure Information:
Title
Virological success from W0 to W48
Secondary Outcome Measure Information:
Title
Progression of HIV infection
Title
CD4 cell count
Title
Safety
Title
Treatment adherence
Title
Quality of life
Title
Viral mutations
Title
Therapeutic strategy failure
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
HIV infected adults
Antiretroviral treatment since 6 months, with two nucleoside analogues and one or two protease inhibitors
CD4 cell count over 100/mm3
HIV RNA below 400 copies/ml since 6 months
Signed written informed consent
Exclusion Criteria:
Previous treatment with non nucleoside analogue, ddI alone
Pregnancy
Alcool abuse
Acute infection, past neurological or pancreatic disease, biological abnormalities
Chemotherapy or immunotherapy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jean-Michel Molina, MD, PhD
Organizational Affiliation
Service de Maladies Infectieuses, Hôpital Saint-Louis, Paris, 75475, France
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Genevieve Chene, MD, PhD
Organizational Affiliation
INSERM unité 593, Bordeaux, France
Official's Role
Study Director
12. IPD Sharing Statement
Citations:
PubMed Identifier
15717256
Citation
Molina JM, Journot V, Morand-Joubert L, Yeni P, Rozenbaum W, Rancinan C, Fournier S, Morlat P, Palmer P, Dupont B, Goujard C, Dellamonica P, Collin F, Poizot-Martin I, Chene G; ALIZE (Agence Nationale de Recherches sur le SIDA 099) Study Team. Simplification therapy with once-daily emtricitabine, didanosine, and efavirenz in HIV-1-infected adults with viral suppression receiving a protease inhibitor-based regimen: a randomized trial. J Infect Dis. 2005 Mar 15;191(6):830-9. doi: 10.1086/428091. Epub 2005 Feb 10.
Results Reference
result
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Once Daily Antiretroviral Therapy in HIV Infected Adults Treated With HAART
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