Drug intelligence / Profile preview

temozolomide + anlotinib + pembrolizumab

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

Overview

This is a **combination regimen** consisting of temozolomide, anlotinib, and pembrolizumab—three pharmaceutical agents with distinct mechanisms. - **Temozolomide** is an oral alkylating agent that exerts cytotoxic effects by methylating DNA, leading to apoptosis in cancer cells. - **Anlotinib** is an oral small molecule multitargeted tyrosine kinase inhibitor that blocks angiogenesis and tumor proliferation by targeting receptors such as VEGFR, FGFR, PDGFR, and c-Kit. - **Pembrolizumab** is a humanized monoclonal antibody that inhibits PD-1, a checkpoint receptor on T cells, enhancing anti-tumor immunity. This triplet regimen is under clinical investigation for recurrent glioblastoma and potentially other advanced solid tumors, aiming to combine cytotoxic, antiangiogenic, and immunotherapeutic effects for synergistic anti-tumor activity[1][3][5][9].

02

Targets

Genomic DNA basesPDCD1 (Programmed cell death protein 1 receptor)VEGFR-1 (Vascular endothelial growth factor receptor 1)VEGFR2 (Vascular endothelial growth factor receptor 2)VEGFR4 (Vascular endothelial growth factor Receptor-3)KIT (c-KIT proto-oncogene receptor tyrosine kinase)DNAFGFR2 (Keratinocyte growth factor receptor)PDGFRA (Platelet-derived growth factor receptor alpha)

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