Early HIV Therapy in Patients With High CD4 Cell Counts

HIV Clinical Trial

— EARLI  

Official title:

Early Antiretroviral Therapy in Resource Limited Settings in Patients With High CD4+ Cell Counts (EARLI)

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01479634
• Other study ID #: EARLI
• Status: Completed
• Phase: N/A
• First received: November 22, 2011
• Last updated: March 3, 2016
• Start date: October 2011
• Est. completion date: June 2015

Study information

• Verified date: March 2016
• Source: University of California, San Francisco
• Contact: n/a
• Is FDA regulated: No
• Health authority: Uganda: National Council for Science and TechnologyUganda: National Drug AuthorityUganda: Research Ethics CommitteeUnited States: Institutional Review Board
• Study type: Interventional

Clinical Trial Summary

A study of antiretroviral therapy (ART) initiation under a "streamlined model of care" in HIV-positive patients with CD4+ cell counts greater ≥ 250 cells/uL

Description:

After dramatic progress in recent years, HIV care for patients in resource limited settings is rapidly evolving to newer models of care delivery. Governments, non-governmental organizations and charitable foundations are placing increasing scrutiny on the programmatic costs associated with delivering antiretroviral therapy (ART). Given these realities, if the global ART roll-out is to continue successfully, we must develop innovative new ways of providing HIV care and ART that are more efficient, more cost-effective, and tightly integrated within country-level health systems. We must treat more patients with fewer resources, and we need sustainable simple models for ART delivery.

These goals can be accomplished building on several existing knowledge points. First, initiating ART at earlier disease stages and at higher CD4+ cell counts may prevent irreversible immunologic damage, prevent opportunistic infections and non-AIDS-associated morbidities, and may prevent death. International and national HIV policy bodies have increasingly recognized this and adjusted recommendations in this direction. Second, ART initiation at higher CD4+ cell counts is less complex, triggers fewer complications, and is less costly to healthcare systems. Third, patients responding to therapy and doing well require fewer physician-administered follow-up visits. This can allow for "task-shifting" to non-MD providers, and the establishment of tiered healthcare delivery down the spectrum of medical acuity. Fourth, the lack of viral load monitoring is responsible for major structural problems in how we deliver ART, causing delays in recognizing ART failure, preventing clinicians from diagnosing HIV drug resistance, and making the decision to switch a patient to a new ART regimen very error-prone.

The EARLI study is a pilot study that will address and investigate all of the above critical issues. This study will focus exclusively on asymptomatic patients with CD4 cell counts ≥250 cells/uL. These relatively healthier individuals are well suited to a more streamlined approach to ART delivery and healthcare provision.

Primary Objectives:

A. To evaluate the 48 week efficacy of ART initiated in asymptomatic individuals with high CD4+ cell counts (CD4+ > 250 cells/uL) and provided in a "streamlined" mode of care.

B. To evaluate the programmatic costs of streamlined ART delivery to asymptomatic high CD4+ count individuals.

Secondary Objectives:

A. To evaluate the 96 week efficacy of ART initiated in high CD4+ cell count individuals.

B. To identify predictors of retention in care among high CD4+ cell count ART initiators.

C. To assess adverse events among high CD4+ cell count ART initiators.

D. To assess medication adherence among high CD4+ cell count ART initiators.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 279
• Est. completion date: June 2015
• Est. primary completion date: June 2015
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• HIV-1 infection diagnosed by a rapid HIV test or any licensed ELISA test kit and documented in the participant's medical chart and re-verified at the time of study screening (hereafter: "screen date").

• Most recent CD4+ cell count = 250 cells/uL:

Arm A: CD4+ cell count 250-350 cells/uL Arm B: CD4+ cell count >350 cells/uL

• Age = 18 years.

• Residence within a 30 kilometer radius of the Bwizibwera HC-IV.

• Willing to initiate ART if the CD4+ cell count is = 350 cells/uL.

• The following laboratory values obtained at the screening visit:

• Absolute neutrophil count (ANC) = 500 cells/uL

• Hemoglobin = 7.0 g/dL

• Platelet count = 50,000/uL

• ALT (SGPT) = 5 times greater than the upper limit of normal

• Estimated glomerular filtration rate (eGFR) of = 60 mL/minute by the Modification of Diet in Renal Disease (MDRD) formula:

eGFR = 186 * Serum creatinine-1.154 * Age-0.203 * [1.21 if African] * [0.742 if female]

• Ability to swallow oral medications.

• Ability and willingness of participant to give informed written consent.

Exclusion Criteria:

• Receipt at any time prior to study entry of > 7 days cumulative treatment with any ARV or combination of ARVs, except ARVs taken for any length of time during pregnancy for the prevention of mother to child transmission (pMTCT) or ARVs taken for occupational exposure.

• For Arm B participants only: allergy/sensitivity to TDF, FTC, EFV, RTV, LPV or formulations of any of these three medications, or to co-formulated Truvada®.

• Active World Health Organization (WHO) HIV stage 3 or 4 illness

• Pregnancy.

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• HIV

Intervention

Drug:
• Standard ART
Standard Ugandan 3-drug antiretroviral therapy regimen consistent with current practices
• Study-Provided ART
Study provided drugs: Truvada® (one tablet PO daily of fixed dose combination consisting of tenofovir disoproxyl fumarate [TDF] and emtricitabine [FTC]) PLUS Efavirenz [EFV]

Locations

Country	Name	City	State
Uganda	Bwizibwera Level IV Health Center	Bwizibwera	Mbarara district

Sponsors (4)

Lead Sponsor	Collaborator
University of California, San Francisco	Infectious Diseases Research Collaboration, Uganda, Makerere University, Makerere University Joint AIDS Program

Country where clinical trial is conducted

Uganda, 

References & Publications (1)

Jain V, Byonanebye DM, Amanyire G, Kwarisiima D, Black D, Kabami J, Chamie G, Clark TD, Rooney JF, Charlebois ED, Kamya MR, Havlir DV; SEARCH Collaboration. Successful antiretroviral therapy delivery and retention in care among asymptomatic individuals wi — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	48-Week Efficacy	Proportion of patients with virologic suppression (HIV-1 plasma RNA =400 copies/cc) at 48 weeks, stratified by study arm.	When all participants reach 48 weeks on study	No
Primary	Programmatic Costs	Total estimated costs of provider time, medications, diagnostic testing, and healthcare facility infrastructure per patient treated with ART for one year, stratified by study arm	When all participants reach 48 weeks on study	No
Secondary	96-Week and 144-Week Efficacy	Proportion of patients with virologic suppression (HIV-1 plasma RNA =400 copies/cc) at 96 and 144 weeks, stratified by study arm.	When all particiants reach 96 and 144 weeks on study, respectively	No
Secondary	Predictors of Retention in Care	Factors statistically significantly associated with attendance at all scheduled clinical visits throughout the first 48 weeks of ART, and throughout the full 144 week study period, stratified by study arm.	When all participants reach 48 weeks on study, then again 144 weeks on study	No
Secondary	Adverse Event Rates	Describe grade 3 or 4 toxicities (defined by NIH DAIDS scale) that occur throughout the first 48 weeks of ART, and throughout the full 144 week study period, stratified by study arm. These will be assessed by active and passive ascertainment and clinical verification, stratified by study arm.	When all participants reach 48 weeks on study, then again at 144 weeks	Yes
Secondary	Medication Adherence	Proportion of total medication doses taken by patients at 48 weeks, assessed by pharmacy refill records, stratified by study arm.	When all participants reach 48 weeks on study	No

External Links

•   MU-UCSF Research Collaboration website