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Afamitresgene Autoleucel: First Approval.
- 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