Golimumab
A fully human monoclonal antibody that inhibits tumor necrosis factor-alpha, a key driver of inflammation in conditions such as rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis, and inflammatory bowel disease. It is administered by subcutaneous injection monthly or intravenously for certain indications. Patients should be screened for tuberculosis and other infections before starting treatment.
Áreas terapéuticas
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.
Preguntas frecuentes
A fully human monoclonal antibody that inhibits tumor necrosis factor-alpha, a key driver of inflammation in conditions such as rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis, and inflammatory bowel disease. It is administered by subcutaneous injection monthly or intravenously for certain indications. Patients should be screened for tuberculosis and other infections before starting treatment.
Yes, Golimumab is an approved drug. It has reached clinical phase 4. It is classified as a Antibody.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL1201833. Open-access bioactivity database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-08-20.
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