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Fludarabine (Flud)

Technische Universität Dresden · FDA-approved active Small molecule

Fludarabine is a purine analog that inhibits ribonucleotide reductase and DNA polymerase, leading to disruption of DNA synthesis and cell death in rapidly dividing cells.

Fludarabine is a purine analog that inhibits ribonucleotide reductase and DNA polymerase, leading to disruption of DNA synthesis and cell death in rapidly dividing cells. Used for Chronic lymphocytic leukemia (CLL), Follicular lymphoma, Small lymphocytic lymphoma (SLL).

At a glance

Generic nameFludarabine (Flud)
SponsorTechnische Universität Dresden
Drug classPurine analog antimetabolite
TargetRibonucleotide reductase, DNA polymerase
ModalitySmall molecule
Therapeutic areaOncology
PhaseFDA-approved

Mechanism of action

Fludarabine is a fluorinated purine nucleoside analog that is phosphorylated intracellularly to its active form, fludarabine triphosphate. This active metabolite inhibits ribonucleotide reductase and DNA polymerase, preventing DNA synthesis and repair. It is particularly effective against lymphoid malignancies because lymphocytes have high levels of deoxycytidine kinase, the enzyme responsible for its activation.

Approved indications

Common side effects

Key clinical trials

Primary sources

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