COLUMVI (glofitamab) by Roche is cd20-directed antibody interactions [moa]. Approved for bispecific cd20-directed cd3 t cell engager [epc]. First approved in 2023.
Drug data last refreshed 3d ago
CD20-directed Antibody Interactions
Bispecific CD20-directed CD3 T Cell Engager
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
TPG: Tafasitamab, Polatuzumab Vedotin, and Glofitamab as First-line Therapy for Diffuse Large B-cell Lymphoma and High-grade B-cell Lymphoma
Glofitamab as a Bridge to and/or Consolidation Post Autologous Stem Cell Transplant in Patients With Relapsed B Cell Lymphomas
Study With Glofitamab in Patients With MCL and Inadequate Response or Relapse Following CAR T-cell Therapy
Double-T - Improving Outcomes in High-risk 2nd Line Relapsed/Refractory Large B-Cell Lymphoma Patients Eligible for CAR-T-cell Therapy With a Glofitamab-based Induction and Consolidation Concept
Gut Microbiome in DLBCL Treated With Glofitamab
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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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