Drug intelligence / Profile preview

brigimadlin + ezabenlimab + BI 754111

Development stage
Unknown
Lead developer
Boehringer Ingelheim
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
Administration
Oral, Intravenous
01

Overview

Brigimadlin + ezabenlimab + BI 754111 is a combination regimen involving three investigational agents developed by Boehringer Ingelheim: - **Brigimadlin (BI 907828):** An oral small-molecule inhibitor that antagonizes MDM2–p53 interaction, restoring p53 tumor suppressor activity and inducing cell-cycle arrest and apoptosis in TP53 wild-type tumors. - **Ezabenlimab (BI 754091):** A monoclonal antibody targeting the programmed death-1 (PD-1) receptor, acting as an immune checkpoint inhibitor to enhance antitumor immune responses. - **BI 754111:** A monoclonal antibody targeting lymphocyte-activation gene 3 (LAG-3), another immune checkpoint protein; this component was included in a triplet regimen in early trials but has since been discontinued. This triplet was studied in a phase I clinical trial setting for advanced/metastatic solid tumors, primarily in patients with biliary tract cancer with MDM2 amplification and TP53 wild-type status. Only one patient in early trials received the full triplet (brigimadlin + ezabenlimab + BI 754111) before discontinuation of BI 754111 from further development[1][4].

Other names
brigimadlin + ezabenlimab + BI 754111
02

Targets

MDM2 (Mouse double minute 2 homolog)PDCD1 (Programmed cell death protein 1 receptor)TP53 (Cellular Tumor Antigen p53 R175H)

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