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3-Year Outcomes for Dolutegravir (DTG) + Lamivudine (3TC) in ART-Naive and Pre-Treated People Living with HIV-1 (PLHIV) in Germany: Real-world Data From the German URBAN Cohort
3-Year Outcomes for Dolutegravir (DTG) + Lamivudine (3TC) in ART-Naive and Pre-Treated People Living with HIV-1 (PLHIV) in Germany: Real-world Data From the German URBAN Cohort
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Systematic Literature Review of Real-world Experience with the 2-Drug Regimen Dolutegravir + Lamivudine (DTG + 3TC) in People with HIV-1 (PWH) Aged > 50 Years
Systematic Literature Review of Real-world Experience with the 2-Drug Regimen Dolutegravir + Lamivudine (DTG + 3TC) in People with HIV-1 (PWH) Aged > 50 Years
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Real-world effectiveness of Dolutegravir + Lamivudine (DTG + 3TC) in Treatment-Naïve People with HIV-1 (PWH) and Low CD4+ Cell Count or High Viral Load at Baseline: A Systematic Literature Review
Real-world effectiveness of Dolutegravir + Lamivudine (DTG + 3TC) in Treatment-Naïve People with HIV-1 (PWH) and Low CD4+ Cell Count or High Viral Load at Baseline: A Systematic Literature Review
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No significant difference in incident hypertension observed by gender, race, baseline BMI or other key subgroups through week 96 among People Living With HIV-1 (PLWH) Receiving Dolutegravir (DTG)-Based Regimens or Comparator Antiretroviral Therapy (cART) in Pooled Randomized Clinical Trials
No significant difference in incident hypertension observed by gender, race, baseline BMI or other key subgroups through week 96 among People Living With HIV-1 (PLWH) Receiving Dolutegravir (DTG)-Based Regimens or Comparator Antiretroviral Therapy (cART) in Pooled Randomized Clinical Trials
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CARAVEL: evaluation of real-world antiviral effectiveness and sustainability of the 2-drug regimen Dolutegravir/Lamivudine Fixed Dose Combination (FDC) in treatment-naïve adults and pre-treated adults who are virologicaly suppressed, in routine clinical care, in France. One-year interim analysis results.
CARAVEL: evaluation of real-world antiviral effectiveness and sustainability of the 2-drug regimen Dolutegravir/Lamivudine Fixed Dose Combination (FDC) in treatment-naïve adults and pre-treated adults who are virologicaly suppressed, in routine clinical care, in France. One-year interim analysis results.
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Efficacy, safety, and implementation outcomes of cabotegravir + rilpivirine long-acting by country in the cabotegravir and rilpivirine implementation study in European locations (CARISEL)
Efficacy, safety, and implementation outcomes of cabotegravir + rilpivirine long-acting by country in the cabotegravir and rilpivirine implementation study in European locations (CARISEL)
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Early and Durable Reductions in Soluble CD14 Concentrations Among Treatment-Experienced Persons With HIV-1 Through 96 Weeks of Fostemsavir Treatment in a Phase 2b Clinical Trial
Early and Durable Reductions in Soluble CD14 Concentrations Among Treatment-Experienced Persons With HIV-1 Through 96 Weeks of Fostemsavir Treatment in a Phase 2b Clinical Trial
Sustained Improvements in Biomarkers Observed With Fostemsavir in Heavily Treatment-Experienced Adults With Multidrug-Resistant HIV-1 From the Phase 3 BRIGHTE Study Through Week 240
Sustained Improvements in Biomarkers Observed With Fostemsavir in Heavily Treatment-Experienced Adults With Multidrug-Resistant HIV-1 From the Phase 3 BRIGHTE Study Through Week 240
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Safety and Tolerability of VH3810109 (N6LS) Among Antiretroviral Therapy–Naive Adults Living With HIV-1: Results From the Monotherapy Phase of the Phase IIa BANNER Study
Safety and Tolerability of VH3810109 (N6LS) Among Antiretroviral Therapy–Naive Adults Living With HIV-1: Results From the Monotherapy Phase of the Phase IIa BANNER Study
Efficacy and Safety of the HIV-1 Maturation Inhibitor GSK3640254 (GSK’254) as Part of a 2-Drug Regimen (2DR) in Treatment-Naive Adults: 24-Week Results from the Phase IIb DYNAMIC Study
Efficacy and Safety of the HIV-1 Maturation Inhibitor GSK3640254 (GSK’254) as Part of a 2-Drug Regimen (2DR) in Treatment-Naive Adults: 24-Week Results from the Phase IIb DYNAMIC Study
Efficacy and Safety of the HIV-1 Maturation Inhibitor GSK3640254 + 2 NRTIs in Treatment-Naive Adults: 24-Week Results From the Phase IIb, Randomized, Dose-Range Finding DOMINO Study
Efficacy and Safety of the HIV-1 Maturation Inhibitor GSK3640254 + 2 NRTIs in Treatment-Naive Adults: 24-Week Results From the Phase IIb, Randomized, Dose-Range Finding DOMINO Study
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