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Azacitidine combined HHT

Shandong Provincial Hospital · Phase 3 active Small molecule

Azacitidine inhibits DNA methyltransferase to reactivate silenced tumor suppressor genes, while HHT (homoharringtonine) inhibits protein synthesis to induce apoptosis in leukemic cells.

Azacitidine inhibits DNA methyltransferase to reactivate silenced tumor suppressor genes, while HHT (homoharringtonine) inhibits protein synthesis to induce apoptosis in leukemic cells. Used for Acute myeloid leukemia (AML), Myelodysplastic syndrome (MDS).

At a glance

Generic nameAzacitidine combined HHT
Also known asAzacitidine+HHT
SponsorShandong Provincial Hospital
Drug classHypomethylating agent combined with protein synthesis inhibitor
TargetDNA methyltransferase (DNMT) and eukaryotic translation elongation factor 2 (eEF-2)
ModalitySmall molecule
Therapeutic areaOncology
PhasePhase 3

Mechanism of action

Azacitidine is a hypomethylating agent that reverses aberrant DNA methylation in myelodysplastic and hematologic malignancies, restoring expression of tumor suppressors. Homoharringtonine (HHT) is a natural alkaloid that inhibits translation elongation, triggering apoptosis particularly in leukemic blasts. The combination targets both epigenetic dysregulation and protein synthesis, providing complementary mechanisms against hematologic malignancies.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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