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Adriamycin, cyclophosphamide, vindesine, valproic acid

European Lung Cancer Working Party · Phase 2 active Small molecule

Adriamycin is an anthracycline antibiotic that intercalates DNA strands, inhibiting topoisomerase II, and inducing apoptosis. Cyclophosphamide is an alkylating agent that cross-links DNA, causing cell death. Vindesine is a vinca alkaloid that binds to tubulin, disrupting microtubule formation and cell division. Valproic acid is a histone deacetylase inhibitor that modulates gene expression.

Adriamycin is an anthracycline antibiotic that intercalates DNA strands, inhibiting topoisomerase II, and inducing apoptosis. Cyclophosphamide is an alkylating agent that cross-links DNA, causing cell death. Vindesine is a vinca alkaloid that binds to tubulin, disrupting microtubule formation and cell division. Valproic acid is a histone deacetylase inhibitor that modulates gene expression. Used for Metastatic breast cancer, Metastatic ovarian cancer, Metastatic non-small cell lung cancer, Multiple myeloma.

At a glance

Generic nameAdriamycin, cyclophosphamide, vindesine, valproic acid
SponsorEuropean Lung Cancer Working Party
Drug classanthracycline antibiotic, alkylating agent, vinca alkaloid, histone deacetylase inhibitor
TargetDNA, tubulin, histone deacetylases
ModalitySmall molecule
Therapeutic areaOncology
PhasePhase 2

Mechanism of action

Adriamycin's mechanism involves the formation of free radicals that damage DNA, leading to cell death. Cyclophosphamide's mechanism involves the formation of DNA cross-links that prevent DNA replication and transcription. Vindesine's mechanism involves the disruption of microtubule formation, which is essential for cell division. Valproic acid's mechanism involves the inhibition of histone deacetylases, which leads to the modulation of gene expression and the induction of apoptosis.

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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