Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
CT-011 + FOLFOX is an investigational combination treatment regimen composed of the **monoclonal antibody CT-011** (which targets the immunological checkpoint receptor PD-1, also called PDCD1), and the established chemotherapy combination **FOLFOX**. FOLFOX itself comprises **folinic acid (leucovorin), fluorouracil (5-FU), and oxaliplatin**. CT-011 blocks PD-1, thereby preventing immune evasion by tumor cells and enhancing T-cell mediated anti-tumor activity (a checkpoint inhibitor mechanism). FOLFOX acts as a cytotoxic regimen that disrupts DNA synthesis and function in rapidly dividing cancer cells. The combination is under investigation for synergistic effects in cancer therapy, particularly in gastrointestinal cancers, with a rationale that immunotherapy (CT-011) can improve the efficacy of chemotherapy (FOLFOX) by activating the immune system alongside direct cytotoxic activity.
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 CT-011 + FOLFOX.