Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This is a combination chemotherapy regimen used primarily in the treatment of metastatic breast cancer. The regimen substitutes capecitabine for 5-fluorouracil (5-FU) in the classic CMF (cyclophosphamide, methotrexate, fluorouracil) protocol. Capecitabine is an oral prodrug that mimics continuous infusion of 5-FU and is converted to its active form preferentially within tumor cells. Cyclophosphamide is an alkylating agent that interferes with DNA replication, while methotrexate is an antimetabolite that inhibits DNA synthesis and repair[1][3]. The combination has shown feasibility and activity in clinical studies for advanced breast cancer[1].
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on capecitabine + cyclophosphamide + methotrexate.