BLAINJECTIONINJECTABLE
Approved
Jul 2013
Lifecycle
Peak
Competitive Pressure
30/100
Clinical Trials
20
Data completeness
5/8 — Partial
SIMPONI ARIA (golimumab) by Johnson & Johnson is tumor necrosis factor receptor blocking activity [moa]. Approved for tumor necrosis factor blocker [epc]. First approved in 2013.
Drug data last refreshed 19h ago · AI intelligence enriched 3w ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
SIMPONI ARIA (golimumab) is a monoclonal antibody TNF-receptor blocker administered via intravenous injection, approved by the FDA on July 18, 2013. It is indicated for the treatment of inflammatory conditions including rheumatoid arthritis, ankylosing spondylitis, psoriatic arthritis, and ulcerative colitis. The drug works by blocking tumor necrosis factor (TNF), a key inflammatory cytokine driving autoimmune and inflammatory diseases. SIMPONI ARIA represents the intravenous formulation of golimumab and occupies a mature position in the competitive TNF-blocker landscape.
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Mechanism of Action
Tumor Necrosis Factor Receptor Blocking Activity
Pharmacologic Class:
Tumor Necrosis Factor Blocker
Indications
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Clinical Trials (20)
Golimumab and Apalutamide for the Treatment of Castration-Resistant Prostate Cancer, TRAMP Study
Started May 2024
8 enrolled
Metastatic Castration-Resistant Prostate CarcinomaProstate AdenocarcinomaStage IV Prostate Cancer AJCC v8
Guselkumab vs Golimumab in PsA TNF Inadequate Responder Patients
Started Jul 2023
63 enrolled
Psoriatic Arthritis
A Study of Combination Therapy With Guselkumab and Golimumab in Participants With Moderately to Severely Active Ulcerative Colitis
Started Sep 2022
577 enrolled
Colitis, Ulcerative
A Study of Combination Therapy With Guselkumab and Golimumab in Participants With Moderately to Severely Active Crohn's Disease
Started Jul 2022
703 enrolled
Crohn's Disease
A Study of Guselkumab and Golimumab Combination Therapy in Participants With Active Psoriatic Arthritis
Started Oct 2021
91 enrolled
Arthritis, Psoriatic
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Data Sources
- Drug label: DailyMed / FDA
- Clinical trials: ClinicalTrials.gov
- Patent data: FDA Orange Book
- Spending data: CMS Medicare
The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.