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Sponsored by: |
National Institute of Allergy and Infectious Diseases (NIAID) |
Information provided by: | National Institute of Allergy and Infectious Diseases (NIAID) |
ClinicalTrials.gov Identifier: | NCT00118898 |
Currently, the preferred anti-HIV regimens used in the United States consist of two nucleoside reverse transcriptase inhibitors (NRTIs) and the nonnucleoside reverse transcriptase inhibitor (NNRTI) efavirenz (EFV). However, with new anti-HIV drugs being approved, alternative regimens need to be tested to determine if new drug combinations have increased effectiveness in treating HIV. The purpose of this study is to test the safety, tolerability, and effectiveness of four different regimens in HIV-infected adults who have never taken anti-HIV drugs.
Condition | Intervention | Phase |
HIV Infections |
Drug: Abacavir/Lamivudine Drug: Atazanavir Drug: Efavirenz Drug: Emtricitabine/Tenofovir disoproxil fumarate Drug: Ritonavir Drug: Abacavir/Lamivudine placebo Drug: Emtricitabine/Tenofovir disoproxil fumarate placebo |
Phase III |
MedlinePlus related topics: | AIDS |
ChemIDplus related topics: | Abacavir Abacavir sulfate Lamivudine Efavirenz Ritonavir Atazanavir sulfate BMS 232632 Tenofovir Tenofovir disoproxil Tenofovir Disoproxil Fumarate |
Study Type: | Interventional |
Study Design: | Other, Randomized, Open Label, Active Control, Parallel Assignment, Safety/Efficacy Study |
Official Title: | A Phase IIIB, Randomized Trial of Open-Label Efavirenz or Atazanavir With Ritonavir in Combination With Double-Blind Comparison of Emtricitabine/Tenofovir or Abacavir/Lamivudine in Antiretroviral-Naive Subjects |
Enrollment: | 1864 |
Study Start Date: | September 2005 |
Primary Completion Date: | December 2007 (Final data collection date for primary outcome measure) |
Arms | Assigned Interventions |
1: Experimental
Participants will receive EFV, FTC/TDF, and placebo for ABC/3TC for 96 weeks
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Drug: Efavirenz
600 mg tablet taken orally daily
Drug: Emtricitabine/Tenofovir disoproxil fumarate
200 mg emtricitabine/300 mg tenofovir disoproxil fumarate tablet taken orally daily
Drug: Abacavir/Lamivudine placebo
Placebo tablet taken orally daily
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2: Experimental
Participants will receive EFV, placebo for FTC/TDF, and ABC/3TC for 96 weeks
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Drug: Abacavir/Lamivudine
600 mg abacavir/300 mg lamivudine tablet taken orally daily
Drug: Efavirenz
600 mg tablet taken orally daily
Drug: Emtricitabine/Tenofovir disoproxil fumarate placebo
Placebo tablet taken orally daily
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3: Experimental
Participants will receive RTV-boosted ATV, FTC/TDF, and placebo for ABC/3TC for 96 weeks
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Drug: Atazanavir
300 mg tablet taken orally daily
Drug: Emtricitabine/Tenofovir disoproxil fumarate
200 mg emtricitabine/300 mg tenofovir disoproxil fumarate tablet taken orally daily
Drug: Ritonavir
100 mg tablet taken orally daily
Drug: Abacavir/Lamivudine placebo
Placebo tablet taken orally daily
|
4: Experimental
Participants will receive RTV-boosted ATV, placebo for FTC/TDF, and ABC/3TC for 96 weeks
|
Drug: Abacavir/Lamivudine
600 mg abacavir/300 mg lamivudine tablet taken orally daily
Drug: Atazanavir
300 mg tablet taken orally daily
Drug: Ritonavir
100 mg tablet taken orally daily
Drug: Emtricitabine/Tenofovir disoproxil fumarate placebo
Placebo tablet taken orally daily
|
Antiretroviral (ARV) treatment regimens consisting of EFV and two NRTIs are the most commonly prescribed regimens for the initial therapy of HIV-infected people in the United States. Such regimens are popular because the drugs are easy to administer, have overall excellent efficacy, and are well tolerated. However, because of concerns about long-term drug toxicity, the development of drug resistance, and potential complications in pregnant women, it is imperative that other drug combinations be investigated as possible alternative initial regimens. Drugs recently approved by the Food and Drug Administration (FDA) for HIV treatment include the protease inhibitor (PI) atazanavir (ATV) and the two NRTI coformulations emtricitabine/tenofovir disoproxil fumarate (FTC/TDF) and abacavir/lamivudine (ABC/3TC). Data are limited on the efficacy of these new drugs when part of anti-HIV drug regimens. This study will evaluate and compare the safety, tolerability, and efficacy of four different treatment regimens in HIV-infected treatment-naive adults.
The treatment portion of this study will last 96 weeks. Participants will be followed for an additional 48 weeks after the treatment portion is completed. Participants will be randomly assigned to one of four arms:
NOTE: Lopinavir/ritonavir may be used in substitution of other drugs for certain participants.
There will be 16 study visits that will occur at study entry; Weeks 1, 2, 4, 8, 16, and 24; and every 12 weeks thereafter. A physical exam, blood collection, and urine collection will occur at most visits. Two pharmacokinetic blood samples will be collected from participants between Weeks 4 and 24. Participants will undergo adherence training at study entry and will be asked to complete adherence questionnaires at selected study visits. Some participants will be asked to participate in ACTG A5224s, a metabolic substudy of ACTG A5202.
Ages Eligible for Study: | 16 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
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Show 64 Study Locations |
Study Chair: | Eric Daar, MD | Harbor-UCLA Medical Center, Los Angeles Biomedical Research Institute |
Study Chair: | Paul Sax, MD | Division of Infectious Diseases, Brigham and Women's Hospital |
Responsible Party: | DAIDS ( Rona Siskind ) |
Study ID Numbers: | ACTG A5202, ACTG 5224s |
First Received: | July 7, 2005 |
Last Updated: | September 26, 2008 |
ClinicalTrials.gov Identifier: | NCT00118898 |
Health Authority: | United States: Federal Government |
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