ZEVALIN (ibritumomab tiuxetan) by Spectrum Dynamics is cd20 antigen (human b-lymphocyte-restricted differentiation antigen, bp35). Approved for refractory, low-grade, follicular b-cell non-hodgkin's lymphoma (nhl) () and 3 more indications. First approved in 2002.
Drug data last refreshed 14h ago · AI intelligence enriched 1mo ago
ZEVALIN is a radiolabeled monoclonal antibody that targets CD20 antigen on B-cell lymphomas, combining ibritumomab (anti-CD20 mAb) with yttrium-90 radioisotope for targeted cytotoxicity. It treats refractory and low-grade follicular B-cell non-Hodgkin's lymphoma (NHL), including previously untreated disease and patients who achieved complete response to first-line chemotherapy. The drug induces cell death through free radical formation from Y-90 beta emission in target and neighboring malignant cells.
Product is in late-stage lifecycle with moderate competitive pressure (30/100), suggesting contracting brand team and focus on retention rather than growth initiatives.
CD20 antigen (human B-lymphocyte-restricted differentiation antigen, Bp35). The apparent affinity (K D ) of ibritumomab tiuxetan for the CD20 antigen ranges between approximately 14 to 18 nM. The CD20 antigen is expressed on pre-B and mature B lymphocytes and on > 90% of B-cell non-Hodgkin’s…
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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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Safety of Ibritumomab Tiuxetan (Zevalin®) in Combination With a Fludarabine-based Reduced Intensity Conditioning (RIC) Regimen (ZEVALLO 2007)
A Prospective Observational Study to Evaluate the Quality of Life and the Costs in a Real Life Setting in Patients Who Are Treated With 90Y-Zevalin
Working on ZEVALIN offers limited growth opportunity given LOE-approaching lifecycle and zero current linked job openings. This role is best suited for professionals seeking to stabilize a mature product or develop expertise in specialty oncology and nuclear medicine reimbursement.