Satralizumab

CHEMBL3833307 Phase 4 Approved Antibody
Half-Life
Bioavailability
Protein Binding
Molecular Weight
g/mol
LogP
Phase
4

Satralizumab is a humanized anti-interleukin-6 receptor (anti-IL-6R) monoclonal antibody used for the treatment of neuromyelitis optica spectrum disorder (NMOSD) in anti-AQP4 antibody-positive patients. By blocking IL-6 signaling, it reduces B-cell-mediated autoimmune pathology and decreases production of pathogenic AQP4-specific antibodies. It is administered subcutaneously and has demonstrated reduction in relapse rates in clinical trials.

Therapeutic Areas

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.

Frequently Asked Questions

Satralizumab is a humanized anti-interleukin-6 receptor (anti-IL-6R) monoclonal antibody used for the treatment of neuromyelitis optica spectrum disorder (NMOSD) in anti-AQP4 antibody-positive patients. By blocking IL-6 signaling, it reduces B-cell-mediated autoimmune pathology and decreases production of pathogenic AQP4-specific antibodies. It is administered subcutaneously and has demonstrated reduction in relapse rates in clinical trials.

Yes, Satralizumab 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). CHEMBL3833307. Open-access bioactivity database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-08-20.

Medical Disclaimer

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.