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Brief Report: Dolutegravir Plus Abacavir/Lamivudine for the Treatment of HIV-1 Infection in Antiretroviral Therapy-Naive Patients: Week 96 and Week 144 Results From the SINGLE Randomized Clinical Trial

The SINGLE study was a randomized, double-blind, noninferiority study that evaluated the safety and efficacy of 50 mg dolutegravir + abacavir/lamivudine versus efavirenz/tenofovir/emtricitabine in 833 ART-naive HIV-1 + participants. Of 833 randomized participants, 71% in the dolutegravir + abacavir/...

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Autores principales: Walmsley, Sharon, Baumgarten, Axel, Berenguer, Juan, Felizarta, Franco, Florence, Eric, Khuong-Josses, Marie-Aude, Kilby, J. Michael, Lutz, Thomas, Podzamczer, Daniel, Portilla, Joaquin, Roth, Norman, Wong, Deborah, Granier, Catherine, Wynne, Brian, Pappa, Keith
Formato: Online Artículo Texto
Lenguaje:English
Publicado: JAIDS Journal of Acquired Immune Deficiency Syndromes 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4645960/
https://www.ncbi.nlm.nih.gov/pubmed/26262777
http://dx.doi.org/10.1097/QAI.0000000000000790
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author Walmsley, Sharon
Baumgarten, Axel
Berenguer, Juan
Felizarta, Franco
Florence, Eric
Khuong-Josses, Marie-Aude
Kilby, J. Michael
Lutz, Thomas
Podzamczer, Daniel
Portilla, Joaquin
Roth, Norman
Wong, Deborah
Granier, Catherine
Wynne, Brian
Pappa, Keith
author_facet Walmsley, Sharon
Baumgarten, Axel
Berenguer, Juan
Felizarta, Franco
Florence, Eric
Khuong-Josses, Marie-Aude
Kilby, J. Michael
Lutz, Thomas
Podzamczer, Daniel
Portilla, Joaquin
Roth, Norman
Wong, Deborah
Granier, Catherine
Wynne, Brian
Pappa, Keith
author_sort Walmsley, Sharon
collection PubMed
description The SINGLE study was a randomized, double-blind, noninferiority study that evaluated the safety and efficacy of 50 mg dolutegravir + abacavir/lamivudine versus efavirenz/tenofovir/emtricitabine in 833 ART-naive HIV-1 + participants. Of 833 randomized participants, 71% in the dolutegravir + abacavir/lamivudine arm and 63% in the efavirenz/tenofovir/emtricitabine arm maintained viral loads of <50 copies per milliliter through W144 (P = 0.01). Superior efficacy was primarily driven by fewer discontinuations due to adverse events in the dolutegravir + abacavir/lamivudine arm [dolutegravir + abacavir/lamivudine arm, 13 (3%); efavirenz/tenofovir/emtricitabine arm, 48 (11%)] through W144. No treatment-emergent integrase or nucleoside resistance was observed in dolutegravir + abacavir/lamivudine recipients through W144.
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spelling pubmed-46459602015-11-30 Brief Report: Dolutegravir Plus Abacavir/Lamivudine for the Treatment of HIV-1 Infection in Antiretroviral Therapy-Naive Patients: Week 96 and Week 144 Results From the SINGLE Randomized Clinical Trial Walmsley, Sharon Baumgarten, Axel Berenguer, Juan Felizarta, Franco Florence, Eric Khuong-Josses, Marie-Aude Kilby, J. Michael Lutz, Thomas Podzamczer, Daniel Portilla, Joaquin Roth, Norman Wong, Deborah Granier, Catherine Wynne, Brian Pappa, Keith J Acquir Immune Defic Syndr Clinical Science The SINGLE study was a randomized, double-blind, noninferiority study that evaluated the safety and efficacy of 50 mg dolutegravir + abacavir/lamivudine versus efavirenz/tenofovir/emtricitabine in 833 ART-naive HIV-1 + participants. Of 833 randomized participants, 71% in the dolutegravir + abacavir/lamivudine arm and 63% in the efavirenz/tenofovir/emtricitabine arm maintained viral loads of <50 copies per milliliter through W144 (P = 0.01). Superior efficacy was primarily driven by fewer discontinuations due to adverse events in the dolutegravir + abacavir/lamivudine arm [dolutegravir + abacavir/lamivudine arm, 13 (3%); efavirenz/tenofovir/emtricitabine arm, 48 (11%)] through W144. No treatment-emergent integrase or nucleoside resistance was observed in dolutegravir + abacavir/lamivudine recipients through W144. JAIDS Journal of Acquired Immune Deficiency Syndromes 2015-12-15 2015-11-13 /pmc/articles/PMC4645960/ /pubmed/26262777 http://dx.doi.org/10.1097/QAI.0000000000000790 Text en Copyright © 2015 Wolters Kluwer Health, Inc. All rights reserved. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits downloading and sharing the work provided it is properly cited. The work cannot be changed in any way or used commercially.
spellingShingle Clinical Science
Walmsley, Sharon
Baumgarten, Axel
Berenguer, Juan
Felizarta, Franco
Florence, Eric
Khuong-Josses, Marie-Aude
Kilby, J. Michael
Lutz, Thomas
Podzamczer, Daniel
Portilla, Joaquin
Roth, Norman
Wong, Deborah
Granier, Catherine
Wynne, Brian
Pappa, Keith
Brief Report: Dolutegravir Plus Abacavir/Lamivudine for the Treatment of HIV-1 Infection in Antiretroviral Therapy-Naive Patients: Week 96 and Week 144 Results From the SINGLE Randomized Clinical Trial
title Brief Report: Dolutegravir Plus Abacavir/Lamivudine for the Treatment of HIV-1 Infection in Antiretroviral Therapy-Naive Patients: Week 96 and Week 144 Results From the SINGLE Randomized Clinical Trial
title_full Brief Report: Dolutegravir Plus Abacavir/Lamivudine for the Treatment of HIV-1 Infection in Antiretroviral Therapy-Naive Patients: Week 96 and Week 144 Results From the SINGLE Randomized Clinical Trial
title_fullStr Brief Report: Dolutegravir Plus Abacavir/Lamivudine for the Treatment of HIV-1 Infection in Antiretroviral Therapy-Naive Patients: Week 96 and Week 144 Results From the SINGLE Randomized Clinical Trial
title_full_unstemmed Brief Report: Dolutegravir Plus Abacavir/Lamivudine for the Treatment of HIV-1 Infection in Antiretroviral Therapy-Naive Patients: Week 96 and Week 144 Results From the SINGLE Randomized Clinical Trial
title_short Brief Report: Dolutegravir Plus Abacavir/Lamivudine for the Treatment of HIV-1 Infection in Antiretroviral Therapy-Naive Patients: Week 96 and Week 144 Results From the SINGLE Randomized Clinical Trial
title_sort brief report: dolutegravir plus abacavir/lamivudine for the treatment of hiv-1 infection in antiretroviral therapy-naive patients: week 96 and week 144 results from the single randomized clinical trial
topic Clinical Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4645960/
https://www.ncbi.nlm.nih.gov/pubmed/26262777
http://dx.doi.org/10.1097/QAI.0000000000000790
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