Prospective Multicenter Study of the Relationship Between Virological Effectiveness and Compliance in HIV-1-infected Patients Treated With Bictegravir

Last updated: March 31, 2025
Sponsor: Association pour la promotion de la recherche en maladies infectieuses et tropicales dans le Loiret
Overall Status: Active - Recruiting

Phase

N/A

Condition

N/A

Treatment

Adherence measured by MEMS caps

Clinical Study ID

NCT06902142
APREMIT 45 (04)
2024-A01111-46
CO-FR-380-7223
  • Ages > 18
  • All Genders

Study Summary

Modern once-daily antiretroviral therapies have evolved considerably, improving patients' quality of life. However, sub-optimal adherence to antiretroviral therapy (ART) can lead to insufficient viral suppression and the emergence of resistant HIV strains. In particular, several populations encountered in HIV clinical practice face obstacles to optimal adherence.

The investigators propose the prospective multicenter cohort study BICTECAPS, evaluating the effectiveness of the combination therapy bictegravir/emtricitabine/tenofovir alafenamide (B/F/TAF) in routine practice. The investigators hypothesize that the pharmacokinetic profile and genetic barrier provided by B/F/TAF will enable a high rate of virological suppression at low to moderate levels of adherence, probably 100% virological suppression above 70% adherence.

The study is planned to include 120 patients with HIV infection treated with B/F/TAF, over a planned 2-year period with usual follow-up.

The aim of this work is to evaluate virological suppression rates at 6 and 12 months according to adherence levels defined by electronic antiretroviral monitoring caps (MEMS caps) and by intra-cellular TAF assay on blotting paper (dried blood spot, DBS).

The investigators hope to generate real-life data on B/F/TAF use from population groups generally under-represented in clinical trials, including robust measurements of adherence patterns using MEMS caps and DBS.

. Key words : HIV-1 ; B/F/TAF ; Adherence ; Forgiveness

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • People living with HIV-1

  • Age greater than or equal to 18 years

  • Having been informed about the study (non-opposition)

  • Acceptance of the use of electronic antiretroviral monitoring caps (MEMS caps)

  • People treated or starting treatment with bictegravir//emtricitabine/tenofovir (B/F/TAF; antiretroviral treatment naïve, changing treatment, virological failure)

Exclusion

Exclusion Criteria:

  • Pregnant women

  • People living with HIV (PLHIV) living in institutionalization, with guardianship orimpaired judgment (to avoid bias due to unability to assume responsibility fortreatment compliance)

  • PLHIV receiving assistance incompatible with the use of the electronic pillbox.

Study Design

Total Participants: 120
Treatment Group(s): 1
Primary Treatment: Adherence measured by MEMS caps
Phase:
Study Start date:
February 11, 2025
Estimated Completion Date:
September 01, 2027

Study Description

Title Etude multicentrique prospective de la relation entre efficacité virologique et observance chez des patients infectés par le VIH-1 traités par BICTEGRAVIR

Type or research Non interventional research (NIR)

Target population People living with HIV (PLWH)

Objectives Primary objective:

  • To explore the effectiveness of antiretroviral treatment with B/F/TAF by virological suppression rate (plasma HIV-RNA) at 6 months in real life according to adherence patterns defined by electronic antiretroviral monitoring caps (MEMS caps) and by intra-cellular TAF assay.

Secondary objective(s):

  • To explore the effectiveness of antiretroviral treatment with B/F/TAF by the rate of virological suppression (plasma HIV-RNA) at 12 months in real life, according to adherence patterns defined by electronic antiretroviral monitoring caps (MEMS caps).

  • Evaluate the risk of emergence of resistance mutations in cases of HIV RNA replication with B/F/TAF.

  • Evaluate the safety profile of B/F/TAF in real-life practice.

  • Evaluate the quality of life of participants treated with B/F/TAF in real-life practice.

Inclusion Criteria -

  • Person living with HIV-1

  • 18 years of age or older

  • Having been informed about the study (non-opposition)

  • Accepts the use of electronic antiretroviral monitoring caps (MEMS caps)

  • Person treated or starting treatment with bictegravir/emtricitabine/tenofovir (B/F/TAF; antiretroviral treatment naïve, changing treatment, virological failure) Exclusion criteria -

  • Pregnant women

  • People living with HIV (PLHIV) unable to assume responsibility for treatment compliance (impaired judgment, guardianship, institutionalization)

  • PLWH receiving assistance incompatible with the use of the electronic pillbox

Endpoints

Primary :

  • Virological failure at 6 months defined as a confirmed plasma viral load >50 copies/mL or a single plasma viral load >200 copies/mL (HIV RNA).

Secondary :

  • Virological failure at 12 months as defined above

  • Rate of side effects measured by CTCAE V.5

  • Emergence of drug resistance mutations according to ANRS AC11 V35 in case of virological replication

  • Quality of life measured by questionnaires

Procedure(s) or visit(s) added by research none

Nomber of patients 120 patients : Accuracy of at least +/-7% on virological failure rate

Number of centers 8 centers :

  • CHU CAEN NORMANDIE

  • CHU d'Orléans

  • APHP Pitié-Salpêtrière

  • CHU Poitiers

  • CHU Nantes

  • CHD La Roche sur Yon

  • CH de Niort

  • HCL Lyon

Project Milestone

  • Expected start date of inclusions: 01/09/2024

  • Inclusion duration: 2 years

  • Duration of follow-up period: 12 months

  • Planned end of study (issue of final report summary 1 year after last visit to last included subject): 01/09/2027

Connect with a study center

  • CHU de Caen

    Caen, 14000
    France

    Active - Recruiting

  • CHD Vendée

    La Roche sur Yon, 85000
    France

    Site Not Available

  • Hôpitaux Civils de Lyon

    Lyon, 69000
    France

    Site Not Available

  • CHU de Nantes

    Nantes, 44000
    France

    Site Not Available

  • CH de Niort

    Niort, 79000
    France

    Site Not Available

  • CHU d'Orléans

    Orléans, 45100
    France

    Active - Recruiting

  • CHU Pitié-Salpétrière

    Paris, 75013
    France

    Site Not Available

  • CHU de Poitiers

    Poitiers, 86000
    France

    Site Not Available

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