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Afamitresgene Autoleucel: First Approval.

Authors :
Keam SJ
Source :
Molecular diagnosis & therapy [Mol Diagn Ther] 2024 Nov; Vol. 28 (6), pp. 861-866. Date of Electronic Publication: 2024 Oct 15.
Publication Year :
2024

Abstract

Afamitresgene autoleucel (TECELRA <superscript>®</superscript> ), a genetically modified human leukocyte antigen (HLA)-restricted autologous melanoma-associated antigen 4 (MAGE-A4)-directed T cell immunotherapy, is being developed by Adaptimmune Therapeutics plc, for the treatment of solid tumours expressing the MAGE-A4 antigen. In August 2024, afamitresgene autoleucel was approved in the USA under accelerated approval for the treatment of adults with unresectable or metastatic synovial sarcoma who have received prior chemotherapy, are HLA-A*02:01P, -A*02:02P, -A*02:03P or -A*02:06P positive and whose tumour expresses the MAGE-A4 antigen as determined by FDA-approved or cleared companion diagnostic devices. This article summarizes the milestones in the development of afamitresgene autoleucel leading to this first approval for the treatment of advanced synovial sarcoma.<br /> (© 2024. The Author(s), under exclusive licence to Springer Nature Switzerland AG.)

Details

Language :
English
ISSN :
1179-2000
Volume :
28
Issue :
6
Database :
MEDLINE
Journal :
Molecular diagnosis & therapy
Publication Type :
Academic Journal
Accession number :
39404764
Full Text :
https://doi.org/10.1007/s40291-024-00749-3