Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
CV301 is a poxviral-based cancer vaccine designed to stimulate an immune response against tumors expressing the human tumor-associated antigens carcinoembryonic antigen (CEA) and mucin 1 (MUC1). The vaccine uses a prime-boost strategy involving two recombinant viral vectors: modified vaccinia Ankara-Bavarian Nordic (MVA-BN) for priming and fowlpox virus (FPV) for boosting. By encoding both CEA and MUC1, CV301 aims to induce T-cell responses targeting these antigens on cancer cells. It has been evaluated in combination with immune checkpoint inhibitors such as anti-PD-1 therapies (nivolumab, pembrolizumab), durvalumab, and atezolizumab across multiple solid tumor types including non-small cell lung cancer, metastatic colorectal cancer, urothelial carcinoma, and others. Clinical trials have demonstrated that CV301 is generally safe and immunologically active; however, efficacy results have varied by indication[5][6][8].
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 CV301.