Glofitamab

CHEMBL4298092 Phase 4 Đã phê duyệt Antibody
Half-Life
Bioavailability
Protein Binding
Molecular Weight
g/mol
LogP
Phase
4

A bispecific T-cell engaging antibody that simultaneously binds to CD20 on B-cell lymphoma cells and CD3 on T-cells, bringing immune cells into direct contact with cancer cells to trigger their destruction. It is approved for the treatment of relapsed or refractory diffuse large B-cell lymphoma after multiple prior therapies. Cytokine release syndrome is a significant but manageable side effect requiring careful clinical monitoring.

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

A bispecific T-cell engaging antibody that simultaneously binds to CD20 on B-cell lymphoma cells and CD3 on T-cells, bringing immune cells into direct contact with cancer cells to trigger their destruction. It is approved for the treatment of relapsed or refractory diffuse large B-cell lymphoma after multiple prior therapies. Cytokine release syndrome is a significant but manageable side effect requiring careful clinical monitoring.

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, Glofitamab 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). CHEMBL4298092. 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.