Study on Retention in Care and on Clinical Chracteristics of HIV-infected Women Treated With Bictegravir/Emtricitabine/Tenofovir Alafenamide (BIKWO).

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18+
SponsorEnte Ospedaliero Ospedali Galliera

About this trial

Women are an underrepresented population in clinical studies on HIV and antiretroviral therapy. This study aims to help bridge this gap by providing real-world data on therapeutic management with B/F/TAF (Biktarvy) in an exclusively female cohort, aiming to improve treatment personalization and the early identification of risk factors for poor retention and treatment failure in this population.

This study is single-center, ambispective observational. The retrospective component analyzes medical record data from June 2019 (the date BIC/FTC/TAF became available in Italy) to the study data cutoff. The prospective component involves data collection during routine follow-up visits up to December 31, 2027. No diagnostic or therapeutic procedures beyond standard clinical practice are involved.

The study opulation includes adult women (≥18 years of age) with a confirmed diagnosis of HIV-1 infection who have received at least one prescription for BIC/FTC/TAF at the Infectious Diseases Unit of E.O. Ospedali Galliera in Genoa from June 2019 to the present, with a documented follow-up of at least 6 months.

The primary objective of the study is to determine the 12- and 24-month retention-in-care rates among women treated with B/F/TAF (Biktarvy) and to identify factors associated with treatment maintenance and predictors of treatment discontinuation.

Secondary objectives of the study include:

* Percentage of women achieving/maintaining virologic suppression (\<50 copies/mL) at 12 and 24 months during B/F/TAF treatment * Evaluation of treatment persistence with B/F/TAF across different age groups * Analysis of reasons for discontinuing B/F/TAF (adverse events, patient choice, planned switch, other) * Identification of factors associated with virologic failure during B/F/TAF therapy * Evaluation of the impact of menopausal status (pre- vs. post-menopause) on retention and virologic outcomes * Analysis of the effect of the menopausal transition during follow-up on outcomes * Correlation of past virologic history (nadir CD4, peak viremia, previous failures) with outcomes * Evaluation of the impact of prior antiretroviral treatment history (previous lines, drug classes used, documented resistance) * Analysis of demographic and socioeconomic variables associated with treatment persistence and virologic success

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Adult women

at least 18 years

documented HIV-1 infection

actively receiving treatment with BIC/FTC/TAF started between 2019 and enrollment date

Disqualifiers

loss to follow up before 6 months from starting BIC/FTC/TAF

unavailability of data/information on follow up after starting BIC/FTC/TAF

Trial population

HIV-1 infected women followed up at the Infectious Diseases Unit of Galliera Hospital, Genoa, Italy

Trial design

Design model

Cohort

Time perspective

Other

Treatments tested in this trial

  • Bictegravir (BIC) plus Emtricitabine (FTC) plus Tenofovir Alafenamide (TAF)

    Drug

    Evaluation of retention in care and description of clinical characteristics of HIV-infected women treated with Bictegravir (BIC) plus Emtricitabine (FTC) plus Tenofovir Alafenamide (TAF). Most published studies treatment of women with Bictegravir (BIC) plus Emtricitabine (FTC) plus Tenofovir Alafenamide (TAF) recruited very few women and focused on efficacy and safety. This study focuses on partecipants' characteristcs and their interaction with retention in care

Treatment groups

100 Participants
are divided into 1 treatment group
Group A: HIV-infeted women1 intervention

Trial outcomes

Primary outcomes

1

Retention in care rate

Time frame
January 2019-December 2027

Secondary outcomes

Other outcomes

Sponsors and contacts

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