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HIDAC (high dose cytarabine)

Pfizer · Phase 3 active Small molecule

High-dose cytarabine is a nucleoside analog that inhibits DNA synthesis by being incorporated into DNA, leading to cell death in rapidly dividing cells.

High-dose cytarabine is a nucleoside analog that inhibits DNA synthesis by being incorporated into DNA, leading to cell death in rapidly dividing cells. Used for Acute myeloid leukemia (AML), Acute lymphoblastic leukemia (ALL), Non-Hodgkin lymphoma.

At a glance

Generic nameHIDAC (high dose cytarabine)
SponsorPfizer
Drug classNucleoside analog; antimetabolite
TargetDNA polymerase; thymidylate synthase
ModalitySmall molecule
Therapeutic areaOncology
PhasePhase 3

Mechanism of action

Cytarabine is a cytidine analog that is phosphorylated intracellularly and incorporated into DNA, causing chain termination and inhibition of DNA polymerase. At high doses, it achieves greater intracellular accumulation and DNA incorporation, resulting in enhanced cytotoxic effects against leukemic and lymphoma cells. The drug is particularly effective in hematologic malignancies due to the high proliferation rate of these 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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