CIMZIA (certolizumab pegol) by UCB Pharma is tumor necrosis factor receptor blocking activity [moa]. Approved for tumor necrosis factor blocker [epc]. First approved in 2008.
Drug data last refreshed 1h ago · AI intelligence enriched 1w ago
CIMZIA (certolizumab pegol) is a pegylated TNF-alpha inhibitor monoclonal antibody approved in 2008 for inflammatory conditions including rheumatoid arthritis and other autoimmune diseases. It works by blocking tumor necrosis factor receptor activity to suppress immune-mediated inflammation. The drug is administered via subcutaneous injection.
Product is in decline phase with approaching loss of exclusivity; commercial teams are likely focused on lifecycle extension and defending market share against biosimilars and newer mechanisms.
Tumor Necrosis Factor Receptor Blocking Activity
Tumor Necrosis Factor Blocker
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
A Study to Test Efficacy, Safety, and Pharmacokinetics of Certolizumab Pegol in Children and Adolescents With Moderately to Severely Active Crohn's Disease
A Study to Assess the Pharmacokinetics of Certolizumab Pegol in Adults With Active Rheumatoid Arthritis
A Study in Pregnant Women With Chronic Inflammatory Diseases Treated With Cimzia (Certolizumab Pegol)
A Study to Evaluate the Pharmacokinetics, Safety, and Effectiveness of Certolizumab Pegol in Children With Moderate to Severe Chronic Plaque Psoriasis
A Study to Assess How Well Certolizumab Pegol Works in Patients With Moderate to Severe Plaque Psoriasis as Part of Routine Clinical Practice
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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.
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CIMZIA roles are concentrated in commercial defense and payer negotiations as the product enters decline phase; limited clinical development means fewer Medical Affairs expansion opportunities. Career growth on this asset is constrained by market maturity, high competitive pressure, and approaching biosimilar erosion.