Drug intelligence / Profile preview

tucidinostat + rituximab + cyclophosphamide + doxorubicin + vincristine + prednisone

Development stage
Phase 3
Lead developer
Akeso
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
Administration
Oral, Intravenous
01

Overview

This drug is a six-drug combination therapy combining **tucidinostat**, a selective histone deacetylase (HDAC) inhibitor, with the R-CHOP chemotherapy regimen (**rituximab, cyclophosphamide, doxorubicin, vincristine,** and **prednisone**) for hematologic malignancies, especially diffuse large B-cell lymphoma (DLBCL) with MYC and BCL2 double expression. Tucidinostat impairs tumor cell proliferation and survival via epigenetic modulation; rituximab is a monoclonal antibody against CD20 on B cells; cyclophosphamide is an alkylating agent; doxorubicin is an anthracycline cytotoxic agent; vincristine is a microtubule inhibitor; prednisone is a glucocorticoid. The combination is intended to improve efficacy in highly aggressive lymphomas by leveraging multiple mechanisms: targeted immunotherapy, chemotherapy, and epigenetic modulation[1][2][3][4][5].

Brand names
Epidaza
Other names
chidamide plus R-CHOPchidamide combined with R-CHOP
02

Targets

CD20 (B-lymphocyte antigen CD20)DNATOP2A (DNA topoisomerase II)GR (Glucocorticoid receptor)HDAC1 (Histone Deacetylase 1)HDAC10 (Histone Deacetylase 10)HDAC2 (Histone deacetylase 2)HDAC3 (Histone Deacetylase 3)TUBB (Tubulin (alpha and beta subunits))

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