Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**CMV-PEA-15** is a gene therapy construct consisting of the human PEA-15 (phosphoprotein enriched in astrocytes 15) cDNA delivered under control of a cytomegalovirus (CMV) promoter as a non-viral plasmid DNA formulation. This construct is designed to drive the overexpression of PEA-15, a protein with known pro-apoptotic and anti-proliferative properties, in transfected cells. Mechanistically, CMV-PEA-15 sequesters phosphorylated ERK (extracellular signal-regulated kinase) in the cytoplasm, thereby inhibiting downstream nuclear transcription factors Elk-1 and AP-1, resulting in increased apoptosis (mediated by cleaved caspase 3 and 7 activation) and reduced tumor cell proliferation. It has demonstrated anti-tumor efficacy in preclinical models of breast cancer, where it induces apoptosis in both cancer and normal cells, though with higher toxicity versus a cancer-specific vector, T-VISA-PEA-15. The developer is an academic/laboratory group, not a pharmaceutical company, and it is an experimental research tool rather than a marketed pharmaceutical product[2].
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 CMV-PEA-15.