- |||||||||| Intermittent three-drug regimens (i-3DR) as maintenance ART: a meta-analysis including individual participant data (ePosters) - Oct 8, 2023 - Abstract #EACS2023EACS_462;
The breakdown of VF cases by antiretroviral class is depicted in the forest plot (Figure 1) for second generation (G) INSTI (Dolutegravir or Bictegravir, INSTI-2G); INSTI-1G (Raltegravir or Elvitegravir); NNRTI-1G (Efavirenz or Rilpivirine); NNRTI-2G (Etravirine or Doravirine) and boosted protease inhibitor (Darunavir, Lopinavir, Atazanavir) with significant heterogeneity overall (I-squared, 53%, p<0.01). Conclusions :
- |||||||||| Intermittent three-drug regimens (i-3DR) as maintenance ART: a meta-analysis including individual participant data (ePosters) - Oct 8, 2023 - Abstract #EACS2023EACS_461;
The breakdown of VF cases by antiretroviral class is depicted in the forest plot (Figure 1) for second generation (G) INSTI (Dolutegravir or Bictegravir, INSTI-2G); INSTI-1G (Raltegravir or Elvitegravir); NNRTI-1G (Efavirenz or Rilpivirine); NNRTI-2G (Etravirine or Doravirine) and boosted protease inhibitor (Darunavir, Lopinavir, Atazanavir) with significant heterogeneity overall (I-squared, 53%, p<0.01). Conclusions :
- |||||||||| Tivicay (dolutegravir) / ViiV Healthcare
Journal: Virologic Response Following a Switch to Dolutegravir-based Regimen in People Living with HIV/AIDS at a Tertiary Care Center in Nepal. (Pubmed Central) - Oct 5, 2023 Method This is a retrospective cohort study including people living with human immunodeficiency virus/ acquired immunodeficiency syndrome (HIV/AIDS) who were transitioned to Tenofovir/Lamivudine/Dolutegravir previously on other antiretroviral therapy regimens for at least 6 months and who had their viral load test done before transition...Tenofovir/Lamivudine/Efavirenz (47.4%), Zidovudine/ Lamivudine/Nevirapine (22.8%) and Zidovudine/Lamivudine/Efavirenz (17.5%) were the most common antiretroviral regimens before transition...Following the transition, 96.5% of the patients had suppressed viral load of fewer than 40 copies/mL. Conclusion Dolutegravir-based antiretroviral regimen led to untransmittable viral load following a switch from Nevirapine and Efavirenz-based regimen.
- |||||||||| Journal: Risks of metabolic syndrome in the ADVANCE and NAMSAL trials. (Pubmed Central) - Oct 4, 2023
In this analysis, we highlight treatment-emergent metabolic syndrome associated with dolutegravir, likely driven by obesity. Clinicians initiating or monitoring patients on INSTI-based ART must counsel for lifestyle optimisation to prevent these effects.
- |||||||||| Aptivus (tipranavir) / Boehringer Ingelheim, Fetroja (cefiderocol) / Shionogi, Tivicay (dolutegravir) / ViiV Healthcare
FDA event, Journal: In silico identification of potential inhibitors of vital monkeypox virus proteins from FDA approved drugs. (Pubmed Central) - Sep 26, 2023 We identified four potential inhibitors namely, Tipranavir, Cefiderocol, Doxorubicin, and Dolutegravir as candidates for repurposing against monkeypox virus from a library of US FDA approved antiviral and antibiotic drugs using molecular docking and molecular dynamics simulations. The main goal of this in silico study is to identify potential inhibitors against monkeypox virus proteins that can be further experimentally validated for the discovery of novel therapeutic agents against monkeypox disease.
- |||||||||| Tivicay (dolutegravir) / ViiV Healthcare
Journal: Development and validation of an HPLC method for quantification of dolutegravir in human plasma. (Pubmed Central) - Sep 18, 2023 Neural tube defect (NTD) prevalence was 0.08%, 0.08%, and 0.15% for 4902 women on dolutegravir preconception, 17 285 HIV-negative women, and 1320 women on efavirenz preconception, respectively, more definitively refuting the dolutegravir preconception NTD safety signal. The linearity of DTG was good in the range of 0.05-10??g/mL (r
- |||||||||| Dovato (dolutegravir/lamivudine) / ViiV Healthcare, Tivicay (dolutegravir) / ViiV Healthcare
Trial initiation date: Woddol4455: Women in Dual With Dolutegravir (clinicaltrials.gov) - Sep 13, 2023 P3, N=290, Not yet recruiting, with no residual viremia through 48w in arm E/C/F/TAF Initiation date: Mar 2023 --> Oct 2023
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