Yttrium Y 90 Ibritumomab Tiuxetan

CHEMBL2108667 Phase 4 Đã phê duyệt Antibody
Half-Life
Bioavailability
Protein Binding
Molecular Weight
g/mol
LogP
Phase
4

Yttrium-90 ibritumomab tiuxetan (Zevalin) is a radioimmunotherapy agent comprising a murine anti-CD20 IgG1 monoclonal antibody (ibritumomab) conjugated via the DTPA-like chelator tiuxetan to the beta-emitting radioisotope yttrium-90. It delivers targeted radiation to CD20-positive B lymphocytes and surrounding tumor cells (crossfire effect) through antibody-directed tumor localization. It is used for the treatment of relapsed or refractory low-grade, follicular, or transformed B-cell non-Hodgkin lymphoma.

Lĩnh vực điều trị

Cơ chế tác dụng

As a monoclonal antibody, it binds with high specificity to its target antigen, modulating the immune response through mechanisms including receptor blockade, immune cell engagement, or targeted cytotoxicity.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Cơ chế

As a monoclonal antibody, it binds with high specificity to its target antigen, modulating the immune response through mechanisms including receptor blockade, immune cell engagement, or targeted cytotoxicity.

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.

Câu hỏi thường gặp

Yttrium-90 ibritumomab tiuxetan (Zevalin) is a radioimmunotherapy agent comprising a murine anti-CD20 IgG1 monoclonal antibody (ibritumomab) conjugated via the DTPA-like chelator tiuxetan to the beta-emitting radioisotope yttrium-90. It delivers targeted radiation to CD20-positive B lymphocytes and surrounding tumor cells (crossfire effect) through antibody-directed tumor localization. It is used for the treatment of relapsed or refractory low-grade, follicular, or transformed B-cell non-Hodgkin lymphoma.

As a monoclonal antibody, it binds with high specificity to its target antigen, modulating the immune response through mechanisms including receptor blockade, immune cell engagement, or targeted cytotoxicity.

Yes, Yttrium Y 90 Ibritumomab Tiuxetan is an approved drug. It has reached clinical phase 4. It is classified as a Antibody.

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References & Data Sources

  • ChEMBL — European Bioinformatics Institute (EBI). CHEMBL2108667. Open-access bioactivity database.

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

Tuyên bố miễn trách y tế

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.