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BI 891065 + ezabenlimab

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

Overview

**BI 891065 + ezabenlimab** is an investigational combination therapy composed of two agents: BI 891065, an orally available small molecule mimetic of SMAC (Second Mitochondria-derived Activator of Caspases) that inhibits the Inhibitor of Apoptosis (IAP) proteins, and ezabenlimab (BI 754091), an anti-PD-1 monoclonal antibody immune checkpoint inhibitor. The combination is intended to potentiate apoptosis in tumor cells and to enhance anti-tumor immune response, aiming to leverage the synergistic effects of IAP inhibition and PD-1-mediated immune checkpoint blockade. It is developed primarily for the treatment of advanced or metastatic solid tumors, particularly in oncology settings, and has been evaluated in phase 1 clinical trials to determine safety, tolerability, and optimal dosing[2][5][1][3][4][7].

Other names
BI 891065 + BI 754091
02

Targets

PDCD1 (Programmed cell death protein 1 receptor)BIRC2 (Cellular inhibitor of apoptosis protein 1)

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