AIDS 2026

AIDS 2026
July 26-31, 2026
Rio de Janeiro, Brazil

International AIDS Conference 2026 .

Explore more information for Gilead HIV / AIDS therapies
Results (24)

Modeling Strategies to Maximize PrEP Impact in the United States with Twice-Yearly Lenacapavir

Genotypic data from participants screened for the PURPOSE 1 and PURPOSE 2 studies demonstrate low level of overall circulating resistance and no phenotypic resistance to lenacapavir

Increased treatment satisfaction and maintained high health-related quality of life among people with HIV switching to a bictegravir/lenacapavir single-tablet regimen from complex regimens: Results from the Phase 3 ARTISTRY-1 trial

Resistance Profile of the HIV Integrase Strand Transfer Inhibitor GS-3242, a Potent Novel Long-Acting Injectable INSTI in Clinical Development

Endorsement and anticipated challenges to adopting twice-yearly lenacapavir (LEN) for HIV pre-exposure prophylaxis (PrEP) among cisgender men who have sex with men (MSM): Qualitative insights from the PURPOSE 2 trial

Integrating gender-affirming hormone therapy with twice-yearly subcutaneous lenacapavir for HIV prevention: Longitudinal qualitative insights from transgender and nonbinary PURPOSE 2 participants

Experiences with twice-yearly lenacapavir for PrEP in the PURPOSE 1 open-label extension phase

Optimizing STI Testing Frequency Among PrEP Users: Implications for Long-Acting HIV Prevention in the Real-world Setting

Favorable Tolerability of Lenacapavir for PrEP Administered at Participant-Chosen Anatomic Sites in PURPOSE 1 and PURPOSE 2

Efficacy and safety of BIC/LEN single-tablet regimen in virologically suppressed people with HIV aged ≥65 Years: Week 48 analysis of participants in the Phase 3 portion of ARTISTRY-1

Pharmacokinetic data supporting the safety and efficacy of BIC/LEN in Phase 3 studies

Efficacy and safety of single-tablet BIC/LEN compared with B/F/TAF in maintaining virologic suppression across age, sex, race, and geographic region subgroups in ARTISTRY-2

Metabolic changes at 48 weeks in people with HIV and virologic suppression switching to single-tablet bictegravir/lenacapavir from complex antiretroviral regimens: Results from the Phase 3 ARTISTRY-1 trial

Immune Biomarker Characterization of Amtabafusp (ABF), a Bispecific T-cell Engager, in a Phase 1b study in People with HIV

Baseline and Week 48 Resistance Analyses in the Phase 3 ARTISTRY-1 Study Evaluating the Bictegravir/Lenacapavir Single-Tablet Regimen

High Efficacy of Twice-Yearly Subcutaneous Lenacapavir for PrEP Through 52 Weeks of Open-Label Extension in PURPOSE 2

Efficacy and Safety of Twice-Yearly Lenacapavir, Teropavimab, and Zinlirvimab as an HIV-1 Treatment Up to 104 Weeks

Long-term safety and efficacy of elvitegravir/cobicistat/emtricitabine/tenofovir alafenamide in treatment-naïve adolescents and virologically suppressed children with HIV-1

Low incidence of treatment-emergent resistance to bictegravir/emtricitabine/tenofovir alafenamide under real-world adherence conditions among people with HIV in the United States, 2018-2024

Outcomes in treatment-experienced (TE) people with HIV (PWH) and detectable viremia switching to bictegravir/emtricitabine/tenofovir alafenamide (B/F/TAF) in routine clinical practice: 24-month (M) results from the BICSTaR study

Once-weekly oral islatravir/lenacapavir (ISL/LEN) versus daily standard-of-care therapy in virologically suppressed adults with HIV-1: Week 48 results of the ISLEND-2 Phase 3 trial

Zero HIV infections with twice-yearly subcutaneous lenacapavir for PrEP during 52 weeks of open-label extension in PURPOSE 1

Once-weekly oral islatravir/lenacapavir (ISL/LEN) versus daily bictegravir/emtricitabine/tenofovir alafenamide (B/F/TAF) in virologically suppressed adults with HIV-1: Week 48 results of the ISLEND-1 Phase 3 trial

Long-term efficacy and safety of bictegravir/emtricitabine/tenofovir alafenamide (B/F/TAF) in children and adolescents with HIV-1 aged 2 to <18 years