- |||||||||| Tybost (cobicistat) / Gilead, Prezista (darunavir) / J&J, Biktarvy (bictegravir/emtricitabine/tenofovir alafenamide) / Gilead
Screening characteristics of participants in an open label, multi?centre, randomized controlled trial investigating integrase inhibitor versus boosted protease inhibitor antiretroviral therapy for late presenters with advanced HIV disease (LAPTOP) () - Oct 26, 2024 - Abstract #HIVGlasgow2024HIV_Glasgow_316; LAPTOP is a 48-week, open-label, European, multi-centre, non-inferiority, controlled trial comparing outcomes for people with advanced HIV disease randomized 1:1 to receive bictegravir (BIC) or darunavir (DRV)/cobicistat (c) co-formulated with emtricitabine (FTC)/tenofovir alafenamide (TAF)...96.5% and 97.9% were fully susceptible to BIC/FTC/TAF or DRV/c/FTC/TAF, respectively (Table 1)... Almost half of LAPTOP trial participants were diagnosed after an AIDS-defining condition was present, and over half had CD4 counts less than 50 cells/
- |||||||||| Biktarvy (bictegravir/emtricitabine/tenofovir alafenamide) / Gilead
Global survey to evaluate engagement in care and treatment experiences of people with HIV () - Oct 26, 2024 - Abstract #HIVGlasgow2024HIV_Glasgow_298; The overall median 10-item HIV Treatment Satisfaction Questionnaire status version score was 54/60 (n = 328); for daily oral ART, median scores were highest among those on bictegravir/emtricitabine/tenofovir alafenamide, 57/60 (n = 51)...P163: Figure 1Open in figure viewerPowerPoint Participants were asked to rank their top three treatment features, among 13 possible responses, that would be most important in remaining on HIV treatment over the long term and their top three reasons that would be most important in switching HIV treatment. Treatment features selected by >25% of participants are shown.
- |||||||||| bictegravir (GS-9883) / Gilead, Pifeltro (doravirine) / Merck (MSD), Biktarvy (bictegravir/emtricitabine/tenofovir alafenamide) / Gilead
Safety and efficacy of doravirine plus tenofovir alafenamide/emtricitabine/bictegravir (TAF/FTC/BIC) in heavily pre?treated patients () - Oct 26, 2024 - Abstract #HIVGlasgow2024HIV_Glasgow_277; Prior ARV was INSTI based in 12 cases (52%), PI based in one (4%), and both INSTI and PI in 10 (43%), with additional maraviroc in three cases (13%)...Among the four subjects with persistent low-grade viraemia, two changed to long-acting cabotegravir/rilpivirine with virological success, and two maintained the combination with last available HIV RNA of 1.82 and 1.90 logs, respectively. The use of DOR plus TAF/FTC/BIC in heavily pre-treated patients was safe
- |||||||||| Biktarvy (bictegravir/emtricitabine/tenofovir alafenamide) / Gilead
Bictegravir/emtricitabine/tenofovir alafenamide (Biktarvy () - Oct 26, 2024 - Abstract #HIVGlasgow2024HIV_Glasgow_259; BFTAF has been used in people with a broad range of NRTI mutations in our clinic of which the most common was M184I/V in isolation; smaller numbers had multiple mutations including seven with K65R. Viral suppression was maintained in 108/117 (92%) of those with NRTI mutations remaining on BFTAF and with follow up of at least 24 weeks.
- |||||||||| Biktarvy (bictegravir/emtricitabine/tenofovir alafenamide) / Gilead
Effectiveness of switching to B/F/TAF in virologically suppressed people with HIV and with pre?existing resistance?associated mutations in Italy: the BIC?BARRIER Study () - Oct 26, 2024 - Abstract #HIVGlasgow2024HIV_Glasgow_253; aFor age, gender, ethnicity, HIV subtype, year of BIC initiation, number of previous regimens failure, HIV-RNA at switch, time from last available GRT and previous gap in care. bFor ethnicity, HIV subtype, year of BIC initiation, HIV-RNA at switch, time from last available GRT and previous gap in care.
- |||||||||| Biktarvy (bictegravir/emtricitabine/tenofovir alafenamide) / Gilead
Antiretroviral treatment with BIC/FTC/TAF: where we come from and where we are going () - Oct 26, 2024 - Abstract #HIVGlasgow2024HIV_Glasgow_237; Antiretroviral therapy with BIC/FTC/TAF is the most commonly used ART in our hospital, being a safe therapy that is generally maintained over time and suitable for PLWH co-infected with HBV. The main reason for discontinuation is the participant's desire to switch to intramuscular therapies.
- |||||||||| Dovato (dolutegravir/lamivudine) / ViiV Healthcare, Biktarvy (bictegravir/emtricitabine/tenofovir alafenamide) / Gilead
Demographic and clinical characteristics of treatment na () - Oct 26, 2024 - Abstract #HIVGlasgow2024HIV_Glasgow_226; Following balancing on population differences, HCPs' reasons for choice varied when comparing B/F/TAF and DTG/3TC. These results warrant additional studies to understand HCP perceptions of ART and PWH key groups' needs.
- |||||||||| Biktarvy (bictegravir/emtricitabine/tenofovir alafenamide) / Gilead
Effectiveness and safety of BIC/FTC/TAF for late?presenting people with HIV?1 infection (Virtual) - Oct 26, 2024 - Abstract #HIVGlasgow2024HIV_Glasgow_218; These results warrant additional studies to understand HCP perceptions of ART and PWH key groups' needs. BIC/FTC/TAF demonstrated robust virological suppression and tolerability in late-presenting PWH.
- |||||||||| doravirine/islatravir (MK-8591A) / Merck (MSD)
Enrollment closed: DOR/ISL in HIV-1 Antiretroviral Treatment-na (clinicaltrials.gov) - Oct 21, 2024 P3, N=500, Active, not recruiting, The observed rates of emergent RAMs at VF were 4% with BIC/FTC/TAF, 8.5% with DTG/ABC/3TC, 18% with DTG/3TC and 39% with DTG/RPV. Recruiting --> Active, not recruiting
- |||||||||| Biktarvy (bictegravir/emtricitabine/tenofovir alafenamide) / Gilead
Journal, Adherence: B/F/TAF forgiveness to non-adherence. (Pubmed Central) - Oct 17, 2024 Given this, an elevated forgiveness plays a relevant role to further improve long-term outcomes and should be considered a fundamental characteristic of any antiretroviral regimen. B/F/TAF has been proved to have all of these characteristics.
- |||||||||| Biktarvy (bictegravir/emtricitabine/tenofovir alafenamide) / Gilead
DRUG INDUCED LIVER INJURY: A UNUSUAL CASE OF CHOLESTATIC HEPATITIS CAUSED BY HIGHLY ACTIVE ANTI-RETROVIRAL THERAPY (HAART) () - Oct 15, 2024 - Abstract #AASLD2024AASLD_1933; Multiple pathogenic mechanisms are reported including direct drug toxicity, immune reconstitution, hypersensitivity reaction and mitochondrial toxicity. Liver toxicity ranges from asymptomatic mild elevation of transaminases with spontaneous resolution to liver failure and death.Current best practice involves maintaining a high level of clinical suspicion and conducting thorough hepatological investigations, guided by the international RUCAM criteria, a diagnostic algorithm for DILI.
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