Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
The mDCF regimen is a modified chemotherapy protocol developed by Memorial Sloan Kettering Cancer Center (MSKCC) for the treatment of gastric and gastroesophageal junction (GEJ) adenocarcinomas. It consists of docetaxel, cisplatin, and 5-fluorouracil (5-FU), often administered alongside leucovorin. This regimen was specifically designed to mitigate the high levels of toxicity, particularly grade 3/4 neutropenia and gastrointestinal side effects, associated with the standard DCF regimen. Docetaxel, a taxane, functions by stabilizing microtubules and inhibiting cell division. Cisplatin is a platinum-based alkylating agent that induces DNA cross-linking, thereby triggering apoptosis. 5-Fluorouracil is an antimetabolite that inhibits thymidylate synthase, disrupting DNA synthesis. The regimen has been evaluated in Phase II clinical trials (e.g., NCT00515411), including cohorts where it is combined with trastuzumab for patients with HER2-positive metastatic disease.
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 docetaxel + cisplatin + fluorouracil (Memorial Sloan Kettering Cancer Center).