Drug intelligence / Profile preview

pablizumab + apatinib

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

Overview

Pablizumab + apatinib is an investigational combination regimen consisting of a programmed cell death protein 1 (PD-1) inhibitor and a vascular endothelial growth factor receptor 2 (VEGFR-2) tyrosine kinase inhibitor. This combination is primarily being evaluated in clinical trials as a neoadjuvant therapy, often in conjunction with chemotherapy, for patients with resectable stage IIA–IIIA non-small cell lung cancer (NSCLC) who do not harbor EGFR mutations or ALK translocations. Apatinib is an orally bioavailable small molecule that inhibits tumor angiogenesis by selectively blocking VEGFR-2, while pablizumab is a monoclonal antibody designed to inhibit the PD-1 checkpoint, thereby enhancing the immune system's anti-tumor response. The synergy between anti-angiogenic therapy and immune checkpoint inhibition is intended to improve pathological complete response rates and overall surgical outcomes in the neoadjuvant setting.

Other names
pablizumab plus apatinibapatinib plus pablizumab
02

Targets

SRC (Proto-oncogene tyrosine-protein kinase Src)KIT (c-KIT proto-oncogene receptor tyrosine kinase)VEGFR2 (Vascular endothelial growth factor receptor 2)PDCD1 (Programmed cell death protein 1 receptor)RET (Rearranged during transfection receptor tyrosine kinase)

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