Drug intelligence / Profile preview

tucidinostat + apatinib

Development stage
Phase 2
Lead developer
Akeso
Modality
Small Molecules
Administration
Oral
01

Overview

A combination therapy consisting of tucidinostat (formerly known as chidamide), an orally available selective histone deacetylase (HDAC) inhibitor that targets HDAC1, 2, 3, and 10, and apatinib, a tyrosine kinase inhibitor primarily targeting vascular endothelial growth factor receptor-2 (VEGFR-2). This combination is being investigated for its potential synergistic effects in treating various cancers, particularly relapsed or refractory osteosarcoma and advanced esophageal cancer.

Other names
ChidamideRivoceranibTucidinostat and Apatinib
02

Targets

HDAC1 (Histone Deacetylase 1)HDAC10 (Histone Deacetylase 10)HDAC11 (Histone Deacetylase 11)HDAC2 (Histone deacetylase 2)HDAC3 (Histone Deacetylase 3)HDAC8 (Histone Deacetylase 8)KIT (c-KIT proto-oncogene receptor tyrosine kinase)RET (Rearranged during transfection receptor tyrosine kinase)SRC (Proto-oncogene tyrosine-protein kinase Src)VEGFR-1 (Vascular endothelial growth factor receptor 1)VEGFR2 (Vascular endothelial growth factor receptor 2)

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