Tildrakizumab

CHEMBL2108681 Phase 4 承認済み Antibody
Half-Life
Bioavailability
Protein Binding
Molecular Weight
g/mol
LogP
Phase
4

This biologic medication is an injection used to treat moderate to severe plaque psoriasis in adults whose disease has not responded adequately to other treatments. It works by blocking interleukin-23, an immune protein that drives the inflammation responsible for psoriasis plaques. It is typically given as two starter injections four weeks apart, then once every twelve weeks.

治療領域

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.

よくある質問

This biologic medication is an injection used to treat moderate to severe plaque psoriasis in adults whose disease has not responded adequately to other treatments. It works by blocking interleukin-23, an immune protein that drives the inflammation responsible for psoriasis plaques. It is typically given as two starter injections four weeks apart, then once every twelve weeks.

Yes, Tildrakizumab 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). CHEMBL2108681. Open-access bioactivity database.

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

医学的免責事項

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.