Efficacy, Safety & Tolerability of Switching EFV/TDF/FTC to BIC/FTC/TAF in Virologically Suppressed Adults With HIV-1

Phase 4CompletedNCT03502005

Midland Research Group, Inc.100 enrolled

Overview

This study evaluates the efficacy, safety and tolerability of switching from the older, established single tablet regimen of ATRIPLA® (EFV/FTC/TDF) to a new single tablet regimen of BIKTARVY® (BIC/FTC/TAF), in HIV-1 infected adult subjects who are virologically suppressed (HIV-1 RNA\<50 copies/mL).

Therapeutic dosage of the tenofovir disoproxil fumarate (TDF) component of ATRIPLA® requires plasma concentrations of the drug that are associated with nephrotoxicity and decreased bone mineral density. Tenofovir alafenamide fumarate (TAF) has a unique metabolism that results in higher intracellular levels of the active phosphorylated moiety tenofovir-diphosphate. Compared with TDF, the therapeutic dosage of TAF reduces tenofovir plasma concentrations by over 90%. This reduction in plasma concentration results in decreased renal and bone risks. TAF has the potential to improve on the efficacy and safety profile of TDF. Efavirenz, another component of ATRIPLA® is widely associated with neuropsychiatric side-effects, including sleep disturbances, depression, and anxiety. Switching from Efavirenz to an integrase inhibitor is associated with improvements in mood. Bictegravir (BIC) is a novel, once daily integrase inhibitor. It has been shown to have potent antiviral activity, a favorable pharmacokinetic profile, good tolerability and an improved resistance profile when compared to previous integrase inhibitors. In a phase 2 trial investigating previously untreated people with HIV, bictegravir plus emtricitabine and tenofovir alafenamide (BIKTARVY®) vs dolutegravir, plus emtricitabine and tenofovir alafenamide both showed high efficacy up to 24 weeks and both regimens were well tolerated. Additionally, switching HAART experienced patients to BIKTARVY® has been shown to be non-inferior to continuation of regimens containing Atazanavir or Darunavir, when they were given with either lamivudine/abacavir or FTC/TDF. The Investigators plan to evaluate in a real world setting the efficacy, safety and tolerability of switching from the older, established single tablet regimen of ATRIPLA® (EFV/FTC/TDF) to a new single tablet regimen of BIKTARVY® (BIC/FTC/TAF). Within the limitations of a real-world study, Investigators have attempted to replicate the protocol of Gilead Science's Phase 3 study evaluating a switch to BIC/FTC/TAF from dolutegravir plus either FTC/TAF or FTC/TDF14. This will have the potential benefit of comparing different regimen switches as well as potentially adding robustness to the body of data regarding BIC/FTC/TAF.

Study Type

INTERVENTIONAL

Allocation

Purpose

TREATMENT

Masking

NONE

Enrollment

100

Conditions

Human Immunodeficiency Virus

Interventions

bictegravir/emtricitabine/tenofovir alafenamideDRUG

Discontinue ATRIPLA® and initiate BIKTARVY®

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * HIV positive * On a stable antiretroviral regimen consisting of ATRIPLA® for at least the 6 consecutive months preceding Screening Visit. * Plasma HIV-1 RNA concentrations at undetectable levels for at least 6 consecutive months prior to the screening visit and have HIV RNA\< 50 copies/mL at the Screening Visit. * Estimated GFR ≥30mL/min according to the Cockcroft-Gault formula for creatinine clearance. * Hepatic transaminases (AST and ALT) ≤5x upper limit of normal (ULN) * Total bilirubin ≤1.5 mg/dL, or normal direct bilirubin. * Adequate hematologic function (hemoglobin ≥ 8.5g/dL; platelets ≥ 50,000/mm3; absolute neutrophil count ≥1,000/mm3) * Female subjects of reproductive potential using a reliable and consistent method of birth control for at least three months prior to study dosing. Male subjects should use condoms when engaging in intercourse of reproductive potential. * The ability to understand and sign a written informed consent form, which must be obtained prior to initiation of study procedures. Exclusion Criteria: * A new AIDS-defining condition diagnosed within 30 days prior to screening. * Individuals with decompensated cirrhosis. (i.e. ascites, encephalopathy, etc.) * Pregnancy * A history of malignancy within the past 5 years (prior to screening) or ongoing malignancy other than cutaneous Kaposi's sarcoma (KS), basal cell carcinoma, or resected, noninvasive cutaneous squamous carcinoma. Individuals with cutaneous KS are eligible but must not have received any systemic therapy for KS within 30 days prior to baseline. * Active, serious infections (other than HIV-1 infection) requiring parenteral antibiotic or antifungal therapy within 30 days prior to baseline. * Life expectancy \< 1 year. * Subject participation in any clinical trial without prior approval from the Investigator. * Concomitant use of disallowed agents from Table 2 * Participation in any other investigation study 30 days prior to enrollment.

Locations (1)

Midland Research Group, Inc

Oakland Park, Florida, United States

Outcomes

Primary Outcomes

assess proportion of patients who develop increase in HIV-1 RNA viral load of ≥ 50 copies/mL

by week 24

Time frame: 24 weeks

Secondary Outcomes

assess stability of kidney function by serial measuring of serum creatinine mg/dL

weeks 24 and 48

Time frame: 48 weeks

Assess effect on restoration of immune markers by serial measurement of CD4+ cells

weeks 24 and 48

Time frame: 48 weeks

assess effect on lipid cardiovascular risk factors by serial measurement of triglycerides and HDL/LDL cholesterol

weeks 24 and 48

Time frame: 48 weeks

assess proportion of patients who continue to have HIV-1 RNA measured <50 copies/mL

weeks 24 and 48

Time frame: 48 weeks

Assess patient reported outcomes by two validated patient questionnaires Philadelphia Sleep Quality Index and HIV Symptom Index

by week 48

Time frame: 48 weeks

assess patient weight variations from baseline

weeks 24 and 48

Time frame: 48 weeks

Data from ClinicalTrials.gov

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