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Hydralazine and magnesium valproate

National Institute of Cancerología · Phase 3 active Small molecule

This combination uses hydralazine as a vasodilator and magnesium valproate as a histone deacetylase inhibitor to modulate vascular function and epigenetic pathways in cancer treatment.

This combination uses hydralazine as a vasodilator and magnesium valproate as a histone deacetylase inhibitor to modulate vascular function and epigenetic pathways in cancer treatment. Used for Cancer (specific indication not publicly detailed; Phase 3 trial status suggests solid tumor or hematologic malignancy under investigation).

At a glance

Generic nameHydralazine and magnesium valproate
Also known asTRANSKRIP R/L
SponsorNational Institute of Cancerología
Drug classCombination therapy: vasodilator + histone deacetylase inhibitor
TargetHDAC (histone deacetylase); vascular smooth muscle relaxation pathways
ModalitySmall molecule
Therapeutic areaOncology
PhasePhase 3

Mechanism of action

Hydralazine is a direct-acting vasodilator that relaxes vascular smooth muscle and may have immunomodulatory effects. Magnesium valproate (valproic acid) is a histone deacetylase (HDAC) inhibitor that promotes histone acetylation, leading to altered gene expression and potential anti-tumor effects. The combination may work synergistically to inhibit angiogenesis and promote differentiation or apoptosis in cancer cells.

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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