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 19h ago · AI intelligence enriched 3w ago
CIMZIA (certolizumab pegol) is a pegylated TNF-alpha inhibitor monoclonal antibody approved in 2008 for the treatment of rheumatoid arthritis and other inflammatory conditions. It works by blocking tumor necrosis factor (TNF) signaling, a key driver of systemic inflammation. Administered via subcutaneous injection, CIMZIA is a first-generation biologic in the TNF inhibitor class and represents a foundational therapy for moderate-to-severe autoimmune disorders.
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 employment relevance is declining as the product approaches LOE; roles in brand management, medical affairs, and specialty field teams may contract post-biosimilar entry. Currently there are 0 linked open positions for this product. Professionals on this product require deep expertise in biologic rheumatology, payer negotiations, biosimilar competitive strategies, and disease-state management to defend market share against lower-cost alternatives.