Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Cetuximab is a recombinant chimeric human/mouse IgG1 monoclonal antibody that targets the epidermal growth factor receptor (EGFR), inhibiting its activation and downstream signaling, which leads to inhibition of cell proliferation, survival, and tumor progression. It is primarily used in the treatment of colorectal cancer and squamous cell carcinoma of the head and neck[1][3][4]. Cisplatin is a platinum-based chemotherapy agent that forms DNA crosslinks, leading to apoptosis in rapidly dividing cells; it is widely used for various solid tumors including head and neck, lung, ovarian, bladder, and testicular cancers. Capecitabine is an oral prodrug converted to 5-fluorouracil (5-FU) in vivo; it inhibits thymidylate synthase resulting in impaired DNA synthesis. Capecitabine is indicated for breast cancer, gastric cancer, colorectal cancer (including adjuvant therapy), among others[6]. The combination of these agents may be used as part of chemoradiotherapy regimens for certain advanced or metastatic cancers.
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 cetuximab + cisplatin + capecitabine.