Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**CpG-gp-E2** is an investigational therapeutic cancer vaccine developed at the University of California, Irvine. It is a self-assembling, nonviral pyruvate dehydrogenase E2 protein nanoparticle functionalized with a melanoma-associated glycoprotein 100 epitope and CpG oligodeoxynucleotide 1826. The gp100 antigen component is intended to prime gp100-specific cytotoxic CD8-positive T-cell responses against melanoma cells, while CpG activates Toll-like receptor 9-mediated innate immune signaling and promotes antigen-presenting-cell activation. In mouse B16 melanoma models, prophylactic subcutaneous vaccination increased gp100-specific CD8-positive T-cell responses, delayed tumor growth, and prolonged survival; it was also evaluated preclinically with anti-PD-1 therapy.
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 CpG-gp-E2.