Difference between revisions of "Glofitamab (Columvi)"
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From the [https://www.cancer.gov/publications/dictionaries/cancer-drug/def/glofitamab NCI Drug Dictionary]: A bispecific monoclonal antibody, with potential antineoplastic activity. Glofitamab contains two antigen-recognition sites: one for human CD3, a T cell surface antigen, and one for human CD20, a tumor-associated antigen (TAA) that is exclusively expressed on B-cells during most stages of B-cell development and is often overexpressed in B-cell malignancies. Upon administration, glofitamab binds to both T-cells and CD20-expressing B-lineage tumor cells. The resulting cross-linkage may trigger a potent cytotoxic T-lymphocyte (CTL) response against the CD20-expressing tumor B-cells. | From the [https://www.cancer.gov/publications/dictionaries/cancer-drug/def/glofitamab NCI Drug Dictionary]: A bispecific monoclonal antibody, with potential antineoplastic activity. Glofitamab contains two antigen-recognition sites: one for human CD3, a T cell surface antigen, and one for human CD20, a tumor-associated antigen (TAA) that is exclusively expressed on B-cells during most stages of B-cell development and is often overexpressed in B-cell malignancies. Upon administration, glofitamab binds to both T-cells and CD20-expressing B-lineage tumor cells. The resulting cross-linkage may trigger a potent cytotoxic T-lymphocyte (CTL) response against the CD20-expressing tumor B-cells. | ||
− | == | + | ==Diseases for which it is used== |
− | + | *[[Diffuse large B-cell lymphoma]] | |
− | + | *[[Transformed lymphoma]] | |
+ | ==History of changes in FDA indication== | ||
+ | *2023-06-15: Initial accelerated approval for relapsed or refractory [[diffuse large B-cell lymphoma|diffuse large B-cell lymphoma, not otherwise specified (DLBCL, NOS)]] or [[Transformed lymphoma|large B-cell lymphoma (LBCL) arising from follicular lymphoma]], after two or more lines of systemic therapy. ''(Based on NP30179)'' | ||
==Also known as== | ==Also known as== | ||
− | *'''Code | + | *'''Code name:''' RO-7082859 |
− | + | *'''Generic name:''' glofitamab-gxbm | |
+ | *'''Brand name:''' Columvi | ||
[[Category:Drugs]] | [[Category:Drugs]] | ||
[[Category:Intravenous medications]] | [[Category:Intravenous medications]] | ||
− | + | [[Category:Anti-CD20-CD3 bispecific antibodies]] | |
− | [[Category:Anti-CD20 | ||
− | |||
− | [[Category:Diffuse large B-cell lymphoma medications | + | [[Category:Diffuse large B-cell lymphoma medications]] |
+ | [[Category:Transformed lymphoma medications]] | ||
− | [[Category: | + | [[Category:FDA approved in 2023]] |
Latest revision as of 00:13, 18 October 2023
Mechanism of action
From the NCI Drug Dictionary: A bispecific monoclonal antibody, with potential antineoplastic activity. Glofitamab contains two antigen-recognition sites: one for human CD3, a T cell surface antigen, and one for human CD20, a tumor-associated antigen (TAA) that is exclusively expressed on B-cells during most stages of B-cell development and is often overexpressed in B-cell malignancies. Upon administration, glofitamab binds to both T-cells and CD20-expressing B-lineage tumor cells. The resulting cross-linkage may trigger a potent cytotoxic T-lymphocyte (CTL) response against the CD20-expressing tumor B-cells.
Diseases for which it is used
History of changes in FDA indication
- 2023-06-15: Initial accelerated approval for relapsed or refractory diffuse large B-cell lymphoma, not otherwise specified (DLBCL, NOS) or large B-cell lymphoma (LBCL) arising from follicular lymphoma, after two or more lines of systemic therapy. (Based on NP30179)
Also known as
- Code name: RO-7082859
- Generic name: glofitamab-gxbm
- Brand name: Columvi