Ciltacabtagene Autoleucel

CHEMBL4802263 Phase 4 承認済み Gene
Half-Life
Bioavailability
Protein Binding
Molecular Weight
g/mol
LogP
Phase
4

Genetic engineering of a patient's own T cells produces ciltacabtagene autoleucel, a chimeric antigen receptor therapy directed at BCMA, a protein expressed on myeloma plasma cells. The modified cells are reinfused and recognise that antigen directly, and in heavily pretreated disease the approach has produced deep and durable remissions. Its place in therapy is relapsed or refractory multiple myeloma after several previous lines. The characteristic hazards belong to the cellular class rather than to conventional pharmacology: cytokine release syndrome and neurotoxicity can be severe and require specialised monitoring, which restricts administration to centres equipped for it. The product is classified as a gene therapy and has completed the final phase of clinical development.

A CAR-T cell therapy in which a patient's own T cells are genetically engineered to express chimeric antigen receptors targeting the BCMA protein on myeloma cells, used for relapsed or refractory multiple myeloma after multiple prior lines of therapy. Infusion of these modified cells can produce deep and durable remissions in heavily pretreated patients. Potentially serious adverse effects include cytokine release syndrome and neurotoxicity requiring specialized monitoring.

治療領域

Pharmacokinetics (PK)

Pharmacodynamics (PD)

HBD / HBA

- / -

No targets recorded

Target interaction data is not yet available for this drug.

No interactions recorded

Drug interaction data is not yet available for this compound.

No side effects recorded

Side effect data is not yet available for this drug.

よくある質問

A CAR-T cell therapy in which a patient's own T cells are genetically engineered to express chimeric antigen receptors targeting the BCMA protein on myeloma cells, used for relapsed or refractory multiple myeloma after multiple prior lines of therapy. Infusion of these modified cells can produce deep and durable remissions in heavily pretreated patients. Potentially serious adverse effects include cytokine release syndrome and neurotoxicity requiring specialized monitoring.

Yes, Ciltacabtagene Autoleucel is an approved drug. It has reached clinical phase 4. It is classified as a Gene.

{# References & Data Sources section for drug detail pages. Renders standard pharmacological database links plus the drug's data_sources field. #}

References & Data Sources

  • ChEMBL — European Bioinformatics Institute (EBI). CHEMBL4802263. Open-access bioactivity database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-08-20.

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This content is for educational and informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider before making medication decisions.

Data sources: ChEMBL, PubChem, DailyMed.