Safety and Efficacy of Reduced Versus Standard Dose Efavirenz (EFV) Plus Two Nucleotides in Antiretroviral-naïve Adults.

Kirby Institute636 enrolled

Overview

Clinical data suggests that the standard dose of the anti-HIV medication, efavirenz (EFV), could be reduced without compromising its effectiveness. Lower drug doses could have fewer side effects and would make EFV more affordable. The purpose of this study is to compare the safety and effectiveness, over 96 weeks, of standard (600mg) versus reduced dose (400mg) EFV in controlling HIV as part of initial combination antiretroviral therapy.

In this international, multicenter trial, 630 HIV infected patients who have not received any previous treatment for their HIV-infection will be enrolled. Participants will be randomized equally (1:1) to receive Truvada (tenofovir and emtricitabine) with either the standard or reduced dose of EFV. Neither the study doctor nor the participant will know which treatment the participant is receiving. Physical examinations, laboratory analyses and questionnaires will be performed at the 11 study visits at screening, baseline (Week 0), Weeks 4, 12, 24, 36, 48, 60, 72, 84 and 96. The primary aim of this study is to compare between treatment groups the proportion of patients with undetectable HIV viral load (HIV RNA \< 200 copies/mL) after 48 weeks. Information on immune function, drug adherence, resistance to antiretrovirals, quality of life, mental state and HIV-related conditions will also be collected. Blood samples will be collected for future testing. Interim analyses will be performed when the first 125 participants in each treatment group reach week 24 and when all participants reach week 24. These interim analyses will provide an early check that the reduced dose of EFV suppresses HIV infection as effectively as the standard dose of EFV. A follow-up analysis will be performed when all participants reach week 96.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

DOUBLE

Enrollment

636

Conditions

HIV Infections

Interventions

Efavirenz 600mgDRUG

3 x EFV 200 milligram (mg) tablets once daily

Efavirenz 400mgDRUG

2 x EFV 200 milligram (mg) tablets plus 1x matched EFV placebo tablet once daily

Eligibility

Sex: ALLMin age: 16 Years

Medical Language ↔ Plain English

Inclusion Criteria: * HIV-1 positive by licensed diagnostic test * aged \>16 years of age (or minimum age as determined by local regulations or as legal requirements dictate) * 50 \< cluster of differentiation (CD)4 \<500 cells/µL * No prior AIDS-defining illness, using the Center for Diseases Control 1993 Case Definition (except pulmonary tuberculosis) * HIV RNA ≥1000 copies/mL * no prior exposure to antiretroviral therapy (ART) (including short course ART for preventing MTCT) * calculated creatinine clearance (CLCr) more than or equal to 50 mL/min (Cockcroft-Gault formula) * provision of written informed consent. Exclusion Criteria: * the following laboratory values: * absolute neutrophil count (ANC) \<500 cells/μL * hemoglobin \<7.0 g/dL * platelet count \<50,000 cells/μL * alanine aminotransferase and/or aspartate aminotransferase \>5 x upper limit of normal * pregnant women or nursing mothers * active opportunistic or malignant disease not under adequate control * use of immunomodulators within 30 days prior to screening * use of any prohibited medications * current alcohol or illicit substance use that might adversely affect study participation

Locations (1)

St Vincent's Hospital

Sydney, New South Wales, Australia

Outcomes

Primary Outcomes

Percentage of Participants With Plasma HIV-1 RNA <200 Copies/mL 48 Weeks After Randomisation

Percentage of participants in each of the treatment arms with centrally quantified plasma HIV-1 RNA viral load \<200 copies/mL 48 weeks after randomisation.

Time frame: 48 weeks

Secondary Outcomes

Percentage of Participants With Plasma HIV-1 RNA <400 Copies/mL and <50 Copies/mL at 48 and 96 Weeks After Randomisation

Percentage of participants in each of the two treatment arms with plasma HIV-1 RNA \<400 copies/mL and \<50 copies/mL at 48 and 96 weeks after randomisation

Time frame: Baseline and 2 years

Mean Change From Baseline in CD4+ T-cell Count

Mean change from baseline to week 96 in CD4+ T-cell count/mm3 between the two treatment arms

Time frame: Baseline and 2 years

Clinical Endpoints: Opportunistic Disease or Death, and Serious Non-AIDS-defining Events and Non-AIDS-related Mortality

Number of participants in each randomised arm diagnosed with a serious non-AIDS defining event, who die from an AIDS-defining event, who die from a non-AIDS-defining event

Time frame: up to 2 years

Change From Baseline in Metabolic Endpoints

Change from baseline to week 96 in fasted total cholesterol, high density cholesterol and low density cholesterol, and glucose between randomised treatment arms

Time frame: Baseline and 2 years

Adherence: Median Scores of Self-reported Adherence to Randomised Study Medications

AIDS Clinical Trials Group (ACTG) 7-day adherence questionnaire scores. Maximum value is all pills taken every day; minimum value is no pills taken per day. Higher scores indicate a better outcome.

Data from ClinicalTrials.gov

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