Drug intelligence / Profile preview

Cyclophosphamide + Epidoxorubicin + Fluorouracil + Methotrexate + Mitomycin-C + Vincristine + Vindesine

Development stage
Unknown
Lead developer
Takeda
Modality
Nucleic Acid-Directed Small Molecules → Small Molecules, Covalent Small Molecules → Small Molecules, Classical Binding Small Molecules → Small Molecules
Administration
Intravenous
01

Overview

This seven-drug combination chemotherapy regimen, "cyclophosphamide + epidoxorubicin + fluorouracil + methotrexate + mitomycin-c + vincristine + vindesine," is described as a multi-agent regimen primarily for advanced breast cancer. The provided search results indicate that while this exact combination is not specifically mentioned, there are references to similar combination therapies that include several of these agents. Related regimens mentioned include: * **VAM** (Vincristine, Adriamycin/Doxorubicin, and Mitomycin): Studied in advanced breast cancer patients previously treated with CMF. It showed a 31% response rate in patients who failed prior CMF, with higher rates (53%) for those failing adjuvant CMF compared to those failing CMF for advanced disease (14%). Myelosuppression was moderate, and no cardiac toxicity was observed. * **VEMFAH** (Vincristine, Cyclophosphamide (Endoxan), Methotrexate, 5-Fluorouracil, Adriamycin (Doxorubicin), and Prednisolone): Demonstrated a 77.1% overall response rate (4 complete, 23 partial responses among 35 evaluable cases) in advanced breast cancer. Median survival for responders was 27.0 months vs. 10.3 months for non-responders. Therapy was rarely terminated due to side effects, though 2 patients developed myocardial damage, but cumulative cardiotoxicity was not apparent. * **CMF** (Cyclophosphamide, Methotrexate, and Fluorouracil): A standard regimen often used as first-line or adjuvant therapy. The specific seven-drug combination would likely have a complex toxicity profile, given the number of cytotoxic agents. Potential adverse effects include myelosuppression, cardiotoxicity, neurotoxicity, mucositis, and other common chemotherapy-related toxicities.

02

Targets

TS (Thymidylate synthase)DHFR (Dihydrofolate reductase)TOP2A (DNA topoisomerase II)DNATUBB (Tubulin (alpha and beta subunits))

Beyond the preview

Go deeper on Cyclophosphamide + Epidoxorubicin + Fluorouracil + Methotrexate + Mitomycin-C + Vincristine + Vindesine.

Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.

Clinical trials

Full profile access

Follow clinical development from study design and recruitment through results.

  • Trial phase
  • Status
  • Readouts

Indications & development

Full profile access

Explore development by indication, patient population, and geography.

  • Indications
  • Development status
  • Countries

Licensing & deals

Full profile access

Trace asset ownership, licensing agreements, and commercial partnerships.

  • Partners
  • Deal terms
  • Milestones

Patents & exclusivity

Full profile access

Explore the patent landscape and regulatory exclusivity around an asset.

  • Patents
  • Expiration dates
  • Exclusivity

Competitive landscape

Full profile access

Compare development programs by target, modality, and indication.

  • Competing assets
  • Targets
  • Development stage

Research & analysis

Full profile access

Connect source evidence and development news to your research questions.

  • Publications
  • News
  • Analysis

Bring the full picture into focus.

See how Gosset can support your research on Cyclophosphamide + Epidoxorubicin + Fluorouracil + Methotrexate + Mitomycin-C + Vincristine + Vindesine.

Explore the full profile

Gosset Free

Get started with Gosset.

Enter your work email and we’ll be in touch with next steps.

Work email preferred.

Book a call