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Duvelisib: A 2018 Novel FDA-Approved Small Molecule Inhibiting Phosphoinositide 3-Kinases

Duvelisib (Copiktra(®)) is a dual inhibitor of phosphoinositide 3-kinases (PI3Kδ and PI3Kγ). In 2018, duvelisib was first approved by the Food and Drug Administration (FDA) for the treatment of adult patients with relapsed or refractory chronic lymphocytic leukaemia (CLL)/ small lymphocytic lymphoma...

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Detalles Bibliográficos
Autores principales: Rodrigues, Daniel A., Sagrillo, Fernanda S., Fraga, Carlos A. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6631818/
https://www.ncbi.nlm.nih.gov/pubmed/31064155
http://dx.doi.org/10.3390/ph12020069
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author Rodrigues, Daniel A.
Sagrillo, Fernanda S.
Fraga, Carlos A. M.
author_facet Rodrigues, Daniel A.
Sagrillo, Fernanda S.
Fraga, Carlos A. M.
author_sort Rodrigues, Daniel A.
collection PubMed
description Duvelisib (Copiktra(®)) is a dual inhibitor of phosphoinositide 3-kinases (PI3Kδ and PI3Kγ). In 2018, duvelisib was first approved by the Food and Drug Administration (FDA) for the treatment of adult patients with relapsed or refractory chronic lymphocytic leukaemia (CLL)/ small lymphocytic lymphoma (SLL) after at least two prior therapies. Duvelisib has also been approved under accelerated track for relapsed or refractory follicular lymphoma (FL) after at least two prior systemic therapies. In this review, we provide a series of information about duvelisib, such as the development of clinical trials for LLC/SLL and FL and the steps used for its synthesis.
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spelling pubmed-66318182019-08-19 Duvelisib: A 2018 Novel FDA-Approved Small Molecule Inhibiting Phosphoinositide 3-Kinases Rodrigues, Daniel A. Sagrillo, Fernanda S. Fraga, Carlos A. M. Pharmaceuticals (Basel) Brief Report Duvelisib (Copiktra(®)) is a dual inhibitor of phosphoinositide 3-kinases (PI3Kδ and PI3Kγ). In 2018, duvelisib was first approved by the Food and Drug Administration (FDA) for the treatment of adult patients with relapsed or refractory chronic lymphocytic leukaemia (CLL)/ small lymphocytic lymphoma (SLL) after at least two prior therapies. Duvelisib has also been approved under accelerated track for relapsed or refractory follicular lymphoma (FL) after at least two prior systemic therapies. In this review, we provide a series of information about duvelisib, such as the development of clinical trials for LLC/SLL and FL and the steps used for its synthesis. MDPI 2019-05-06 /pmc/articles/PMC6631818/ /pubmed/31064155 http://dx.doi.org/10.3390/ph12020069 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Brief Report
Rodrigues, Daniel A.
Sagrillo, Fernanda S.
Fraga, Carlos A. M.
Duvelisib: A 2018 Novel FDA-Approved Small Molecule Inhibiting Phosphoinositide 3-Kinases
title Duvelisib: A 2018 Novel FDA-Approved Small Molecule Inhibiting Phosphoinositide 3-Kinases
title_full Duvelisib: A 2018 Novel FDA-Approved Small Molecule Inhibiting Phosphoinositide 3-Kinases
title_fullStr Duvelisib: A 2018 Novel FDA-Approved Small Molecule Inhibiting Phosphoinositide 3-Kinases
title_full_unstemmed Duvelisib: A 2018 Novel FDA-Approved Small Molecule Inhibiting Phosphoinositide 3-Kinases
title_short Duvelisib: A 2018 Novel FDA-Approved Small Molecule Inhibiting Phosphoinositide 3-Kinases
title_sort duvelisib: a 2018 novel fda-approved small molecule inhibiting phosphoinositide 3-kinases
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6631818/
https://www.ncbi.nlm.nih.gov/pubmed/31064155
http://dx.doi.org/10.3390/ph12020069
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