Drug intelligence / Profile preview

apatinib + PD-L1 inhibitor

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

Overview

A combination therapy consisting of apatinib, a small-molecule tyrosine kinase inhibitor, and a programmed death-ligand 1 (PD-L1) inhibitor. Apatinib (also known as rivoceranib) selectively inhibits vascular endothelial growth factor receptor 2 (VEGFR-2), thereby inhibiting tumor angiogenesis and potentially modulating the tumor microenvironment to enhance immune activity. PD-L1 inhibitors are monoclonal antibodies that block the interaction between PD-L1 on tumor cells and the PD-1 receptor on T cells, thereby restoring the anti-tumor immune response. This combination is being investigated as a maintenance therapy for extensive-stage small cell lung cancer (ES-SCLC) in patients who have achieved disease control following initial induction chemotherapy. The rationale for this combination is the potential synergy between anti-angiogenic effects and immune checkpoint blockade to prolong progression-free survival.

Other names
PD-L1 inhibitor + apatinibapatinib + PD-L1 inhibitor
02

Targets

KIT (c-KIT proto-oncogene receptor tyrosine kinase)CD274 (Programmed cell death protein 1 ligand 1)SRC (Proto-oncogene tyrosine-protein kinase Src)ABCB1 (P-glycoprotein)VEGFR2 (Vascular endothelial growth factor receptor 2)ABCG2 (Breast cancer resistance protein)

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