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Cytarabine (Ara-C)

Kura Oncology, Inc. · Phase 3 active Small molecule

Cytarabine is a nucleoside analog that inhibits DNA synthesis by being incorporated into DNA, leading to chain termination and cell death, particularly affecting rapidly dividing cells.

Cytarabine is a nucleoside analog that inhibits DNA synthesis by being incorporated into DNA, leading to chain termination and cell death, particularly affecting rapidly dividing cells. Used for Acute myeloid leukemia (AML), Acute lymphoblastic leukemia (ALL), Chronic myeloid leukemia (CML).

At a glance

Generic nameCytarabine (Ara-C)
Also known ascytosine arabinoside (ara-C), Cytosar-U, Tarabine PFS, ARA-C, Cytosar
SponsorKura Oncology, Inc.
Drug classNucleoside analog; antimetabolite
TargetDNA polymerase; thymidylate synthase
ModalitySmall molecule
Therapeutic areaOncology
PhasePhase 3

Mechanism of action

Cytarabine (Ara-C) is a cytidine analog that is phosphorylated intracellularly and incorporated into DNA during the S phase of the cell cycle. This incorporation causes DNA chain termination and inhibits DNA polymerase, leading to apoptosis of cancer cells. It is particularly effective against hematologic malignancies due to its preferential uptake and metabolism in rapidly dividing cells.

Approved indications

Common side effects

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

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

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