Drug intelligence / Profile preview

chidamide + CHOP

Development stage
Unknown
Lead developer
Akeso
Modality
Orthosteric Ligands → Classical Binding Small Molecules → Small Molecules, Covalent Small Molecules → Small Molecules, Nucleic Acid-Directed Small Molecules → Small Molecules
Administration
Oral, Intravenous
01

Overview

Chidamide + CHOP is a combination therapy consisting of the histone deacetylase inhibitor chidamide and the standard chemotherapy regimen known as CHOP (cyclophosphamide, doxorubicin, vincristine, and prednisone). Chidamide is an oral small molecule that selectively inhibits histone deacetylases (HDACs), leading to altered gene expression and apoptosis in malignant cells. The addition of chidamide to the conventional CHOP regimen has been investigated primarily for angioimmunoblastic T-cell lymphoma (AITL) and other peripheral T-cell lymphomas. Clinical studies have shown that this combination can improve overall survival and response rates compared to CHOP alone in newly diagnosed AITL patients[1][3][9]. The mechanism of action involves both epigenetic modulation by chidamide and cytotoxic effects from the chemotherapeutic agents in CHOP.

Other names
chidamide plus CHOPchidamide combined with CHOP
02

Targets

TOP2A (DNA topoisomerase II)HDAC10 (Histone Deacetylase 10)HDAC1 (Histone Deacetylase 1)GR (Glucocorticoid receptor)DNATUBB (Tubulin (alpha and beta subunits))

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