Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
PSMA alphavaccine (AVX-501) is an experimental cancer vaccine developed by AlphaVax, in collaboration with Progenics Pharmaceuticals and PSMA Development Company, for the treatment of prostate cancer. The vaccine utilizes the Venezuelan Equine Encephalitis (VEE) virus-based replicon particle (VRP) platform. In this system, the structural genes of the VEE virus are replaced with the gene encoding prostate-specific membrane antigen (PSMA), a protein highly expressed on the surface of prostate cancer cells. These single-cycle, self-replicating RNA particles are designed to infect dendritic cells and induce high-level expression of PSMA, thereby triggering both cellular (T-cell) and humoral (antibody) immune responses against the tumor. Clinical evaluation has reached Phase I in patients with metastatic castration-resistant prostate cancer, where it demonstrated good tolerability but modest immunogenicity at the doses tested.
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 PSMA alphavaccine.