Drug intelligence / Profile preview

CDIAG

Development stage
Unknown
Lead developer
First Affiliated Hospital of Soochow University
Modality
Small Molecules, Cytokines & Interferons → Recombinant Proteins and Enzymes
Administration
Intravenous, Oral, Subcutaneous
01

Overview

CDIAG is an investigational **co-administration chemotherapy regimen** for relapsed or refractory acute myeloid leukemia. It combines the epigenetic agents chidamide, a histone deacetylase inhibitor, and decitabine, a DNA methyltransferase inhibitor, with low-dose cytarabine, idarubicin, and granulocyte colony-stimulating factor. The regimen was evaluated as a double epigenetic-priming approach in a Phase 2 study sponsored by The First Affiliated Hospital of Soochow University; the published study enrolled 35 patients and reported a complete remission rate of 42.9% and median overall survival of 11.7 months. ([frontiersin.org](https://www.frontiersin.org/journals/oncology/articles/10.3389/fonc.2021.726926/full))

Other names
CDIAG regimenchidamide + decitabine + cytarabine + idarubicin + granulocyte colony-stimulating factordouble epigenetic priming regimen
02

Targets

DNMT3A (DNA methyltransferase 3 alpha)HDAC1 (Histone Deacetylase 1)DNACSF3R (Granulocyte colony-stimulating factor receptor)DNMT3B (DNA (cytosine-5)-methyltransferase 3B)DNMT1 (DNA (cytosine-5)-methyltransferase 1)TOP2A (DNA topoisomerase II)DNA polymerase familyHDAC10 (Histone Deacetylase 10)

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