Table 4.

Select clinical trials in myeloid malignancies evaluating oral HMAs in combination with cedazuridine

Investigational agent(s)Patient populationTrial number
ASTX030 MDS, CMML, AML NCT04256317 
ASTX030 MDS NCT04608110 
ASTX727 Lower-risk MDS NCT03502668, NCT03906695 
ASTX727 MDS with detectable MRD after allo-HCT NCT04742634 
ASTX727 + itacitinib, INCB053914, or INCB059872 MDS/MPN overlap syndromes NCT04061421 
ASTX727 + venetoclax MDS, CMML NCT04655755 
ASTX727 + venetoclax AML NCT04657081, NCT04746235 
ASTX727 + venetoclax + ivosidenib or enasidenib IDH1 or IDH2-mutated AML NCT04774393 
ASTX727 + ASTX660 AML NCT04155580 
Investigational agent(s)Patient populationTrial number
ASTX030 MDS, CMML, AML NCT04256317 
ASTX030 MDS NCT04608110 
ASTX727 Lower-risk MDS NCT03502668, NCT03906695 
ASTX727 MDS with detectable MRD after allo-HCT NCT04742634 
ASTX727 + itacitinib, INCB053914, or INCB059872 MDS/MPN overlap syndromes NCT04061421 
ASTX727 + venetoclax MDS, CMML NCT04655755 
ASTX727 + venetoclax AML NCT04657081, NCT04746235 
ASTX727 + venetoclax + ivosidenib or enasidenib IDH1 or IDH2-mutated AML NCT04774393 
ASTX727 + ASTX660 AML NCT04155580 

MPN, myeloproliferative neoplasm; MRD, minimal residual disease.

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