Drug intelligence / Profile preview

spartalizumab + LCL161

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

Overview

The combination of **spartalizumab** (a humanized monoclonal antibody targeting PD-1) and **LCL161** (an orally bioavailable small molecule inhibitor of inhibitor of apoptosis proteins, or IAPs) is an investigational therapy studied for advanced and relapsed/refractory cancers such as multiple myeloma. Spartalizumab is an immune checkpoint inhibitor that blocks PD-1, thereby enhancing T cell-mediated anti-tumor responses. LCL161 acts as a SMAC mimetic, antagonizing IAPs, leading to the induction of apoptosis in tumor cells. This combination aims to synergistically enhance anti-tumor immunity and apoptosis in cancer cells. Both drugs are primarily developed by Novartis.

Other names
spartalizumab + LCL161PDR001 + LCL161
02

Targets

PDCD1 (Programmed cell death protein 1 receptor)IAP (Inhibitor of apoptosis protein family)cIAP1 BIR3 (Cellular inhibitor of apoptosis protein 1 (cIAP1) BIR3 domain)

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