Background: In the ART-PRO pilot trial there were no virological failures through 48 weeks of treatment with dolutegravir plus lamivudine in suppressed individuals with and without archived lamivudine resistance-associated mutations (RAMs) detected through next-generation sequencing (NGS) but without evidence of lamivudine RAMs in baseline proviral DNA population sequencing. Objectives: To present 96 week results from ART-PRO. Methods: Open-label, single-arm pilot trial. At baseline, all participants switched to dolutegravir plus lamivudine. Participants were excluded if proviral DNA population genotyping detected lamivudine RAMs. To detect resistance minority variants, proviral DNA NGS was retrospectively performed from baseline samp...
Editor: Recent data from clinical trials highlight the efficacy of a two-drug strategy with lamivudi...
Objectives: We aimed to investigate and compare the efficacy and safety of two dolutegravir-based tw...
Background: Lamivudine (3TC) therapy can cause the emergence of M184I/V. Previous studies suggest a ...
Background: In the ART-PRO pilot trial there were no virological failures through 48 weeks of treatm...
Background We investigated the efficacy of a switch to dolutegravir plus lamivudine in aviremic ind...
We investigated the efficacy of a switch to dolutegravir plus lamivudine in aviremic individuals wit...
Background: Results from clinical trials and observational studies suggest that lamivudine plus dolu...
International audienceOBJECTIVES:To evaluate the dolutegravir+lamivudine combination in virologicall...
Background: Direct comparisons between lamivudine plus bPIs and lamivudine plus dolutegravir as main...
Abstract Background Direct comparisons between lamivudine plus bPIs and lamivudine plus dolutegravir...
To investigate the long-term safety and efficacy of a treatment switch to dual ART with atazanavir/r...
Objectives: The aim of this study was to assess the efficacy of dolutegravir plus lamivudine (DTG + ...
Objectives: This study evaluated the virological efficacy of dolutegravir 50mg twice daily in 190 HI...
Results from clinical trials and observational studies suggest that lamivudine plus dolutegravir cou...
Editor: Recent data from clinical trials highlight the efficacy of a two-drug strategy with lamivudi...
Objectives: We aimed to investigate and compare the efficacy and safety of two dolutegravir-based tw...
Background: Lamivudine (3TC) therapy can cause the emergence of M184I/V. Previous studies suggest a ...
Background: In the ART-PRO pilot trial there were no virological failures through 48 weeks of treatm...
Background We investigated the efficacy of a switch to dolutegravir plus lamivudine in aviremic ind...
We investigated the efficacy of a switch to dolutegravir plus lamivudine in aviremic individuals wit...
Background: Results from clinical trials and observational studies suggest that lamivudine plus dolu...
International audienceOBJECTIVES:To evaluate the dolutegravir+lamivudine combination in virologicall...
Background: Direct comparisons between lamivudine plus bPIs and lamivudine plus dolutegravir as main...
Abstract Background Direct comparisons between lamivudine plus bPIs and lamivudine plus dolutegravir...
To investigate the long-term safety and efficacy of a treatment switch to dual ART with atazanavir/r...
Objectives: The aim of this study was to assess the efficacy of dolutegravir plus lamivudine (DTG + ...
Objectives: This study evaluated the virological efficacy of dolutegravir 50mg twice daily in 190 HI...
Results from clinical trials and observational studies suggest that lamivudine plus dolutegravir cou...
Editor: Recent data from clinical trials highlight the efficacy of a two-drug strategy with lamivudi...
Objectives: We aimed to investigate and compare the efficacy and safety of two dolutegravir-based tw...
Background: Lamivudine (3TC) therapy can cause the emergence of M184I/V. Previous studies suggest a ...