Last reviewed · How we verify

Ixabepilone + Capecitabine

R-Pharm · Phase 3 active Small molecule

Ixabepilone stabilizes microtubules to prevent cell division, while capecitabine is a prodrug that converts to fluorouracil to inhibit DNA synthesis, together providing synergistic cytotoxic activity against cancer cells.

Ixabepilone stabilizes microtubules to prevent cell division, while capecitabine is a prodrug that converts to fluorouracil to inhibit DNA synthesis, together providing synergistic cytotoxic activity against cancer cells. Used for Metastatic or locally advanced breast cancer, HER2-negative breast cancer.

At a glance

Generic nameIxabepilone + Capecitabine
Also known asBMS-247550, IXEMPRA, Epothilone, IXEMPRA®
SponsorR-Pharm
Drug classMicrotubule stabilizer + Antimetabolite
Targetβ-tubulin (ixabepilone); Thymidylate synthase (capecitabine/5-FU)
ModalitySmall molecule
Therapeutic areaOncology
PhasePhase 3

Mechanism of action

Ixabepilone is a microtubule-stabilizing agent (taxane analog) that binds to β-tubulin and prevents microtubule depolymerization, disrupting mitotic spindle formation and inducing apoptosis. Capecitabine is a fluoropyrimidine carbamate that is metabolized to 5-fluorouracil, which inhibits thymidylate synthase and disrupts DNA synthesis. The combination exploits complementary mechanisms of action for enhanced antitumor efficacy.

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: