Drug intelligence / Profile preview

anlotinib + durvalumab

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

Overview

Anlotinib + durvalumab is a combination therapy consisting of anlotinib, a novel oral multitarget tyrosine kinase inhibitor (TKI), and durvalumab, a monoclonal antibody that acts as a programmed death ligand-1 (PD-L1) checkpoint inhibitor. Anlotinib inhibits angiogenesis and tumor cell proliferation by targeting multiple receptor tyrosine kinases involved in tumor growth and vascularization. Durvalumab blocks the interaction between PD-L1 and its receptor PD-1, thereby enhancing anti-tumor immune responses. This combination has been investigated primarily for extensive-stage small cell lung cancer (ES-SCLC), both as part of first-line treatment regimens with chemotherapy and as maintenance therapy after initial chemotherapy response. Early-phase clinical studies suggest potential synergistic effects between these agents, leading to improved progression-free survival (PFS), objective response rate (ORR), and manageable safety profiles in ES-SCLC patients[1][2][3].

Brand names
Imfinzi (for durvalumab)
Other names
anlotinib plus durvalumabanlotinib combined with durvalumab
02

Targets

PDGFRA (Platelet-derived growth factor receptor alpha)VEGFR2 (Vascular endothelial growth factor receptor 2)PDGFRB (Platelet-derived growth factor receptor beta)CD274 (Programmed cell death protein 1 ligand 1)FGFR2 (Keratinocyte growth factor receptor)KIT (c-KIT proto-oncogene receptor tyrosine kinase)FGFR1 (Fibroblast growth factor receptor 1)

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