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denintuzumab mafodotin + rituximab + ifosfamide + carboplatin + etoposide

Development stage
Unknown
Lead developer
Pfizer
Modality
Small Molecules, Cytotoxic ADCs → Antibody-Drug Conjugates (ADCs) → Antibody Conjugates → Antibody-Based Therapeutics, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

This is a combination regimen composed of **denintuzumab mafodotin** (an antibody-drug conjugate targeting CD19), **rituximab** (an anti-CD20 monoclonal antibody), **ifosfamide**, **carboplatin**, and **etoposide** (all cytotoxic chemotherapy agents) designed to treat relapsed or refractory diffuse large B-cell lymphoma (DLBCL) and other B-cell non-Hodgkin lymphomas. Denintuzumab mafodotin acts by selectively delivering a cytotoxic agent to CD19-expressing B cells, while rituximab mediates B-cell depletion through CD20 targeting. The remaining agents are DNA-damaging cytotoxics. The combination exploits non-overlapping mechanisms for B-cell malignancies and is intended to increase efficacy compared to traditional regimens[3][5]. Denintuzumab mafodotin was developed by Seagen.

Other names
denintuzumab mafodotin + R-ICEdenintuzumab mafodotin + rituximab + ICE
02

Targets

CD19 (B lymphocyte antigen CD19)CD20 (B-lymphocyte antigen CD20)TOP2A (DNA topoisomerase II)DNATUBB (Tubulin (alpha and beta subunits))

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