Nivolumab

CHEMBL2108738 Phase 4 معتمد Antibody
Half-Life
27 days
Bioavailability
Protein Binding
Molecular Weight
g/mol
LogP
Phase
4

A checkpoint inhibitor immunotherapy that removes a brake on the immune system, allowing T-cells to recognize and attack cancer cells.

المجالات العلاجية

تصنيفات الأدوية

آلية العمل

Fully human anti-PD-1 IgG4 monoclonal antibody restoring T-cell anti-tumor activity.

Pharmacokinetics (PK)

Half-Life 27 days

Pharmacodynamics (PD)

الآلية

Fully human anti-PD-1 IgG4 monoclonal antibody restoring T-cell anti-tumor activity.

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.

الأسئلة الشائعة

A checkpoint inhibitor immunotherapy that removes a brake on the immune system, allowing T-cells to recognize and attack cancer cells.

Fully human anti-PD-1 IgG4 monoclonal antibody restoring T-cell anti-tumor activity.

Key pharmacokinetic parameters for Nivolumab: Half-life: 27 days.

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

Related Drugs

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References & Data Sources

  • ChEMBL — European Bioinformatics Institute (EBI). CHEMBL2108738. Open-access bioactivity database.

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

إخلاء المسؤولية الطبية

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.