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Authors | Henia Dar, Daniel Henderson, Zinkal Padalia, Ashley Porras, Dakai Mu, Maeng Kyungah, Seshidhar Police, Demetrios Kalaitzidis, Jonathan Terrett, Jason Sagert | ||||||||||||
Title | Preclinical Development of CTX120, an Allogeneic CAR-T Cell Targeting Bcma | ||||||||||||
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URL | https://ashpublications.org/blood/article/132/Supplement%201/1921/261777/Preclinical-Development-of-CTX120-an-Allogeneic | ||||||||||||
Abstract Text | Blood (2018) 132 (Supplement 1): 1921 |
Molecular Profile | Treatment Approach |
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Gene Name | Source | Synonyms | Protein Domains | Gene Description | Gene Role |
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Drug Name | Trade Name | Synonyms | Drug Classes | Drug Description |
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CTX120 | CTX-120|CTX 120 | CTX120 consists of allogeneic T-lymphocytes engineered with CRISPR/Cas9 to insert a BCMA-targeting chimeric antigen receptor (CAR) in the T-cell receptor alpha constant (TRAC) locus, and to simultaneously remove the endogenous T cell receptor (TCR) and MHC class I, which potentially results in increased cytotoxicity against BCMA-expressing tumor cells, and inhibits tumor growth (Blood (2018) 132 (Supplement 1): 1921). |
Gene | Variant | Impact | Protein Effect | Variant Description | Associated with drug Resistance |
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Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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