Ciltacabtagene Autoleucel

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

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.

Therapeutische Bereiche

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.

Häufig gestellte Fragen

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.

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References & Data Sources

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

Data aggregated from publicly available pharmacological databases. Last updated 2026-02-27.

Medizinischer Haftungsausschluss

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.