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Durvalumab: First Global Approval
Intravenous durvalumab (Imfinzi™; AstraZeneca) is a fully human monoclonal antibody that blocks programmed cell death ligand-1 binding to its receptors (PD-1 and CD80), resulting in enhanced T-cell responses against cancer cells. The US FDA has granted durvalumab accelerated approval for the treatme...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer International Publishing
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5636860/ https://www.ncbi.nlm.nih.gov/pubmed/28643244 http://dx.doi.org/10.1007/s40265-017-0782-5 |
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author | Syed, Yahiya Y. |
author_facet | Syed, Yahiya Y. |
author_sort | Syed, Yahiya Y. |
collection | PubMed |
description | Intravenous durvalumab (Imfinzi™; AstraZeneca) is a fully human monoclonal antibody that blocks programmed cell death ligand-1 binding to its receptors (PD-1 and CD80), resulting in enhanced T-cell responses against cancer cells. The US FDA has granted durvalumab accelerated approval for the treatment of patients with locally advanced or metastatic urothelial carcinoma who have disease progression during or following platinum-containing chemotherapy, or within 12 months of neoadjuvant or adjuvant platinum-containing chemotherapy. Durvalumab ± tremelimumab is under phase III clinical trials in urothelial carcinoma, non-small cell lung cancer, small cell lung cancer and head and neck squamous cell carcinoma. The drug is also being evaluated in phase I or II clinical trials in a wide range of solid tumours and haematological malignancies. This article summarizes the milestones in the development of durvalumab leading to this first approval for urothelial carcinoma. |
format | Online Article Text |
id | pubmed-5636860 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-56368602017-10-23 Durvalumab: First Global Approval Syed, Yahiya Y. Drugs AdisInsight Report Intravenous durvalumab (Imfinzi™; AstraZeneca) is a fully human monoclonal antibody that blocks programmed cell death ligand-1 binding to its receptors (PD-1 and CD80), resulting in enhanced T-cell responses against cancer cells. The US FDA has granted durvalumab accelerated approval for the treatment of patients with locally advanced or metastatic urothelial carcinoma who have disease progression during or following platinum-containing chemotherapy, or within 12 months of neoadjuvant or adjuvant platinum-containing chemotherapy. Durvalumab ± tremelimumab is under phase III clinical trials in urothelial carcinoma, non-small cell lung cancer, small cell lung cancer and head and neck squamous cell carcinoma. The drug is also being evaluated in phase I or II clinical trials in a wide range of solid tumours and haematological malignancies. This article summarizes the milestones in the development of durvalumab leading to this first approval for urothelial carcinoma. Springer International Publishing 2017-06-22 2017 /pmc/articles/PMC5636860/ /pubmed/28643244 http://dx.doi.org/10.1007/s40265-017-0782-5 Text en © Springer International Publishing AG 2017 |
spellingShingle | AdisInsight Report Syed, Yahiya Y. Durvalumab: First Global Approval |
title | Durvalumab: First Global Approval |
title_full | Durvalumab: First Global Approval |
title_fullStr | Durvalumab: First Global Approval |
title_full_unstemmed | Durvalumab: First Global Approval |
title_short | Durvalumab: First Global Approval |
title_sort | durvalumab: first global approval |
topic | AdisInsight Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5636860/ https://www.ncbi.nlm.nih.gov/pubmed/28643244 http://dx.doi.org/10.1007/s40265-017-0782-5 |
work_keys_str_mv | AT syedyahiyay durvalumabfirstglobalapproval |