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Lenacapavir: First Approval

Lenacapavir (Sunlenca(®)) is a long-acting capsid inhibitor of human immunodeficiency virus type 1 (HIV-1) being developed by Gilead Sciences Inc. It is available as an oral tablet and injectable solution, with the latter being a slow-release formulation to allow bi-annual subcutaneous administratio...

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Detalles Bibliográficos
Autor principal: Paik, Julia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10267266/
https://www.ncbi.nlm.nih.gov/pubmed/36272024
http://dx.doi.org/10.1007/s40265-022-01786-0
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author Paik, Julia
author_facet Paik, Julia
author_sort Paik, Julia
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description Lenacapavir (Sunlenca(®)) is a long-acting capsid inhibitor of human immunodeficiency virus type 1 (HIV-1) being developed by Gilead Sciences Inc. It is available as an oral tablet and injectable solution, with the latter being a slow-release formulation to allow bi-annual subcutaneous administration. In August 2022, lenacapavir received its first approval in the EU for use in combination with other antiretroviral(s) in adults with multi-drug resistant HIV infection, for whom it is otherwise not possible to construct a suppressive anti-viral regimen. This article summarizes the milestones in the development of lenacapavir leading to this first approval for the treatment of HIV-1 infection. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40265-022-01786-0.
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spelling pubmed-102672662023-06-15 Lenacapavir: First Approval Paik, Julia Drugs AdisInsight Report Lenacapavir (Sunlenca(®)) is a long-acting capsid inhibitor of human immunodeficiency virus type 1 (HIV-1) being developed by Gilead Sciences Inc. It is available as an oral tablet and injectable solution, with the latter being a slow-release formulation to allow bi-annual subcutaneous administration. In August 2022, lenacapavir received its first approval in the EU for use in combination with other antiretroviral(s) in adults with multi-drug resistant HIV infection, for whom it is otherwise not possible to construct a suppressive anti-viral regimen. This article summarizes the milestones in the development of lenacapavir leading to this first approval for the treatment of HIV-1 infection. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40265-022-01786-0. Springer International Publishing 2022-10-22 2022 /pmc/articles/PMC10267266/ /pubmed/36272024 http://dx.doi.org/10.1007/s40265-022-01786-0 Text en © Springer Nature 2022, corrected publication 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visithttp://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle AdisInsight Report
Paik, Julia
Lenacapavir: First Approval
title Lenacapavir: First Approval
title_full Lenacapavir: First Approval
title_fullStr Lenacapavir: First Approval
title_full_unstemmed Lenacapavir: First Approval
title_short Lenacapavir: First Approval
title_sort lenacapavir: first approval
topic AdisInsight Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10267266/
https://www.ncbi.nlm.nih.gov/pubmed/36272024
http://dx.doi.org/10.1007/s40265-022-01786-0
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