Last reviewed · How we verify

pirarubicin and cyclophosphamide

Hebei Medical University Fourth Hospital · FDA-approved active Small molecule

Pirarubicin is an anthracycline that intercalates into DNA and inhibits topoisomerase II, while cyclophosphamide is an alkylating agent that cross-links DNA, together inducing cancer cell death.

Pirarubicin is an anthracycline that intercalates into DNA and inhibits topoisomerase II, while cyclophosphamide is an alkylating agent that cross-links DNA, together inducing cancer cell death. Used for Breast cancer (as part of chemotherapy regimen), Various solid tumors and hematologic malignancies.

At a glance

Generic namepirarubicin and cyclophosphamide
SponsorHebei Medical University Fourth Hospital
Drug classAnthracycline and alkylating agent combination
TargetDNA (topoisomerase II for pirarubicin; DNA alkylation for cyclophosphamide)
ModalitySmall molecule
Therapeutic areaOncology
PhaseFDA-approved

Mechanism of action

Pirarubicin, a derivative of daunorubicin, intercalates between DNA base pairs and inhibits topoisomerase II, preventing DNA unwinding and causing double-strand breaks in rapidly dividing cells. Cyclophosphamide is a nitrogen mustard alkylating agent that forms covalent cross-links in DNA, preventing replication and transcription. This combination targets cancer cells through complementary mechanisms of DNA damage.

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

Competitive intelligence

For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape: