ADCETRIS (brentuximab vedotin) by Pfizer is cd30 is a member of the tumor necrosis factor receptor family and is expressed on the surface of salcl cells and on hodgkin reed-sternberg (hrs) cells in chl. First approved in 2011.
Drug data last refreshed 4h ago · AI intelligence enriched 1w ago
ADCETRIS (brentuximab vedotin) is an antibody-drug conjugate (ADC) that targets CD30-expressing lymphomas, including Hodgkin lymphoma and systemic anaplastic large cell lymphoma. It works by binding to CD30 on tumor cells, internalizing, and releasing MMAE, a microtubule-disrupting agent that induces cell cycle arrest and apoptosis. The drug also demonstrates activity through antibody-dependent cellular phagocytosis.
Peak lifecycle stage indicates mature, stable commercial operations with established infrastructure; moderate competitive pressure (30) suggests focused rather than high-intensity team environment.
CD30 is a member of the tumor necrosis factor receptor family and is expressed on the surface of sALCL cells and on Hodgkin Reed-Sternberg (HRS) cells in cHL. CD30 is variably expressed in other T-cell lymphomas. Expression of CD30 on healthy tissue and cells is limited. In vitro data suggest that…
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Real-life Experience of Brentuximab Vedotin Plus CHP as First-line Treatment of CD30+ Peripheral T-cell Lymphomas in Spain
A Study of Brentuximab Vedotin With Doxorubicin, Vinblastine and Dacarbazine in Adults With Hodgkin Lymphoma in India
Open Label Extension Study of Brentuximab Vedotin in Early dcSSc
A Study in Adults With Cutaneous T-cell Lymphoma (CTCL) Retreated With Brentuximab Vedotin
A Study in Adults With Advanced Classical Hodgkin's Lymphoma (cHL) in Brazil Treated With Brentuximab Vedotin Together With Chemotherapy Compared to Chemotherapy Alone
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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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