Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
A quadruple chemotherapy regimen combining three cytotoxic agents (capecitabine, oxaliplatin, and irinotecan) with the targeted anti-angiogenic monoclonal antibody bevacizumab. This combination targets multiple cancer pathways simultaneously through DNA synthesis inhibition (capecitabine), DNA crosslinking (oxaliplatin), topoisomerase I inhibition (irinotecan), and VEGF-mediated angiogenesis blockade (bevacizumab). ## Mechanism of Action This regimen combines four distinct agents with complementary mechanisms: 1. **Capecitabine**: An oral fluoropyrimidine that converts to 5-fluorouracil in tumor tissue, inhibiting DNA synthesis and cell division. 2. **Oxaliplatin**: A platinum-based compound that forms DNA adducts, preventing DNA replication and transcription. 3. **Irinotecan**: A topoisomerase I inhibitor that prevents DNA unwinding and replication. 4. **Bevacizumab**: A monoclonal antibody that targets vascular endothelial growth factor (VEGF), inhibiting angiogenesis and tumor blood vessel formation. ## Clinical Applications This quadruple regimen has been studied in clinical trials for: - First-line treatment of metastatic colorectal cancer - Treatment of gastrointestinal neuroendocrine carcinoma (NEC) ## Efficacy Data Clinical studies have shown promising results with this combination: - In metastatic colorectal cancer, the regimen has demonstrated median progression-free survival of 10.4-16 months and median overall survival of 24.4-29 months. - For gastrointestinal neuroendocrine carcinoma, the combination showed an overall response rate of 47.4% and median progression-free survival of 13 months. ## Toxicity Profile The combination has significant toxicity, with grade 3/4 adverse events including: - Diarrhea (16-36%) - Vomiting (21%) - Fatigue (17%) - Hematologic toxicities Due to these toxicities, modified dosing regimens have been explored to improve tolerability while maintaining efficacy.
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 + oxaliplatin + irinotecan + bevacizumab.