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Doxorubicin Hydrochloride (doxorubicin)

Pfizer · FDA-approved active Verified Quality 80/100

Doxorubicin works by intercalating DNA strands and inhibiting topoisomerase II, an enzyme essential for DNA replication and cell division.

Doxorubicin Hydrochloride, originally developed by Baxter Holding B.V. and currently owned by Pfizer, is a small molecule anthracycline topoisomerase inhibitor targeting Aurora kinase A. It was FDA-approved in 1974 for various cancer indications, including acute lymphoid and myeloid leukemia, ovarian cancer, and breast cancer. As an off-patent medication, doxorubicin is available from multiple generic manufacturers. Key safety considerations include its potential for cardiotoxicity and myelosuppression. Its bioavailability is relatively low at 5%, with a half-life of 32 hours.

At a glance

Generic namedoxorubicin
SponsorPfizer
Drug classAnthracycline Topoisomerase Inhibitor
TargetAurora kinase A
Therapeutic areaOncology
PhaseFDA-approved
First approval1974

Mechanism of action

The cytotoxic effect of doxorubicin hydrochloride on malignant cells and its toxic effects on various organs are thought to be related to nucleotide base intercalation and cell membrane lipid binding activities of doxorubicin. Intercalation inhibits nucleotide replication and action of DNA and RNA polymerases. The interaction of doxorubicin with topoisomerase II to form DNA-cleavable complexes appears to be an important mechanism of doxorubicin hydrochloride cytocidal activity.

Approved indications

Boxed warnings

Common side effects

Drug interactions

Key clinical trials

Primary sources

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SourceUsed for
FDA labelMechanism, indications, dosing, boxed warnings, drug interactions
ClinicalTrials.govTrial enrolment, design, endpoints, results

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