FTC/RPV/TDF on T-Cell Activation, CD4+ T-Cell Count, Inflammatory Biomarkers and Viral Reservoir
Trial ID or NCT#
Status
NOT RECRUITING
Purpose
This study was done with people who were infected with HIV, but did not show any signs of having HIV. They were also feeling well without taking HIV medication and had low or undetectable levels of the virus in the blood. The purpose of this study was to see if taking HIV medication (antiretroviral therapy [ART]) would reduce immune activation (a signal that the body is fighting an infection) in people who have HIV, but did not show symptoms. Also this study helped determine how safe the drug was and how well people reacted to the drug. For this study, the following antiretroviral therapy (ART) was be provided in the form of a single tablet that contains three different drugs: emtricitabine/rilpivirine/tenofovir disoproxil fumarate (FTC/RPV/TDF). These drugs were combined as one tablet which was approved by the Food and Drug Administration (FDA) as a single pill to treat HIV infection. The HIV medication provided was one of the recommended treatments for HIV, including people with low viral loads (how much HIV you have in your body) who were taking HIV drugs for the first time. The risks seen with this HIV medication were the same that one would encounter when taking these drugs outside of the study.
Official Title
A Prospective, Single-Arm, Open-Label Study to Evaluate the Effect of Fixed-Dose Emtricitabine/Rilpivirine/Tenofovir Disoproxil Fumarate on T-Cell Activation, Absolute CD4+ T-Cell Count, Inflammatory Biomarkers and Viral Reservoir in Treatment-Naïve HIV-1 Controllers
Eligibility Criteria
- Step 1 - HIV-1 infection - ART-naïve defined as ≤7 days of antiretroviral (ARV) treatment at any time prior to entry - Documentation of HIV-1 RNA <500 copies/mL verified by at least two measurements prior to the screening RNA specimen - Screening HIV-1 RNA <500 copies/mL using an US FDA-approved assay obtained within 60 days prior to study entry by any laboratory that has a CLIA certification or its equivalent - Laboratory values obtained within 60 days prior to entry by any laboratory that has a CLIA certification or its equivalent: - Absolute neutrophil count (ANC) >=500/mm^3 - Hemoglobin >=8.0 g/dL - Platelet count >=40,000/mm^3 - Aspartate aminotransferase (AST) (SGOT), alanine aminotransferase (ALT) (SGPT), and alkaline phosphatase <=5 X Upper Limit of Normal (ULN) - Total bilirubin <=2.5 X ULN - Calculated creatinine clearance (CrCl) >=60 mL/min - For females of reproductive potential, negative serum or urine pregnancy test within 48 hours prior to study entry by any clinic or laboratory that has a CLIA certification or its equivalent - Female subjects of reproductive potential, who are participating in sexual activity that could lead to pregnancy, must agree to use at least one reliable form of contraceptive (ie, condoms (male or female) with or without a spermicidal agent; a diaphragm or cervical cap with spermicide; an intrauterine device (IUD); or hormone-based contraceptive) while receiving the protocol-specified treatment and for 6 weeks after stopping the medications - No evidence of any exclusionary resistance mutations based on results from any genotype assay from any laboratory that has a Clinical Laboratory Improvement Amendments (CLIA) certification or its equivalent Step 2 - Completion of Step 1 - Ability and willingness of subject to choose to receive either open-label ART FDC (FTC/RPV/TDF) or no study treatment for an additional 48 weeks - For females of reproductive potential, negative serum or urine pregnancy test within 48 hours prior to the week 60 visit by any clinic or laboratory that has a CLIA certification or its equivalent
- Step 1 - Chronic hepatitis B virus (HBV) infection (documented by hepatitis B surface antigen (HBsAg) seropositivity) - Breastfeeding - Use of immunomodulators (eg, interleukins, interferons, cyclosporine), topical imiquimod, HIV vaccine, systemic cytotoxic chemotherapy, or investigational therapy within 30 days prior to study entry or plans to start immunomodulators, topical imiquimod, HIV vaccine, systemic cytotoxic chemotherapy, or investigational therapy during the study - Known allergy/sensitivity or any hypersensitivity to components of study drug(s) or their formulation - Active drug or alcohol use or dependence that, in the opinion of the site investigator, would interfere with adherence to study requirements - Acute or serious illness requiring systemic treatment and/or hospitalization within 30 days prior to entry - Symptomatic HIV disease and/or AIDS-defining illness. - Vaccinations within 7 days prior to study entry - Plans to initiate hepatitis C treatment during the study - Perinatally-acquired HIV - Use of any of the following medications within 7 days prior to study entry: - St. John's wort (Hypercium perforatum) - Anticonvulsants (eg, oxacarbazepine, phenobarbital, phenytoin) - Anti-infectives (eg, rifabutin, rifampin, rifapentine) - Corticosteroids (eg, dexamethasone (more than 1 dose)) - Proton pump inhibitors (eg, esomeprazole, lansoprazole, omeprazole, pantoprazole, rabeprazole) Step 2 - Plans to start immunomodulators, topical imiquimod, HIV vaccine, systemic cytotoxic chemotherapy, or investigational therapy during Step 2 of the study - Plans to initiate hepatitis C treatment during Step 2 of the study NOTE: Please refer to the protocol for detailed eligibility criteria.
Investigator(s)
Contact us to find out if this trial is right for you.
Contact
Debbie Slamowitz
650 723-2804
View on ClinicalTrials.gov
