Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
A combination chemotherapy regimen consisting of azacitidine, capecitabine, and oxaliplatin. This regimen was studied in Phase I/II clinical trials for colorectal cancer patients, particularly those with CpG island methylator phenotype (CIMP-high) tumors who were refractory to fluoropyrimidine/oxaliplatin treatment. Azacitidine is a DNA methyltransferase inhibitor that was hypothesized to restore sensitivity to fluoropyrimidine and oxaliplatin chemotherapy through epigenetic modulation. The standard dosing schedule includes subcutaneous azacitidine (75 mg/m²/day on days 1-5), intravenous oxaliplatin (110 mg/m² on day 2), and oral capecitabine (1500 mg/m² divided twice daily for 2 weeks) in a three-week cycle.
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 azacitidine + capecitabine + oxaliplatin.