Ublituximab

CHEMBL2108354 Phase 4 Onaylandı Antibody
Half-Life
Bioavailability
Protein Binding
Molecular Weight
g/mol
LogP
Phase
4

Ublituximab is a chimeric monoclonal antibody targeting CD20 on B lymphocytes that depletes CD20-expressing B cells through antibody-dependent cellular cytotoxicity (ADCC) and complement-dependent cytotoxicity (CDC), with glycoengineering to enhance ADCC activity. It is approved for the treatment of relapsing forms of multiple sclerosis and has been investigated in B-cell malignancies including chronic lymphocytic leukemia and non-Hodgkin lymphoma. Its glycoengineered Fc region provides enhanced potency compared to non-engineered anti-CD20 antibodies.

Terapötik Alanlar

Etki Mekanizması

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)

Mekanizma

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.

Sıkça Sorulan Sorular

Ublituximab is a chimeric monoclonal antibody targeting CD20 on B lymphocytes that depletes CD20-expressing B cells through antibody-dependent cellular cytotoxicity (ADCC) and complement-dependent cytotoxicity (CDC), with glycoengineering to enhance ADCC activity. It is approved for the treatment of relapsing forms of multiple sclerosis and has been investigated in B-cell malignancies including chronic lymphocytic leukemia and non-Hodgkin lymphoma. Its glycoengineered Fc region provides enhanced potency compared to non-engineered anti-CD20 antibodies.

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, Ublituximab is an approved drug. It has reached clinical phase 4. It is classified as a Antibody.

{# 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). CHEMBL2108354. Open-access bioactivity database.

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

Tıbbi Sorumluluk Reddi

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.