Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
The prostate-specific antigen (PSA) RNA-pulsed dendritic cell (DC) vaccine is an autologous cellular immunotherapy designed to treat prostate cancer. The therapy involves isolating a patient's own dendritic cells and loading them with messenger RNA encoding the tumor-associated antigen PSA, typically via electroporation or co-incubation. These modified DCs are then reintroduced into the patient to stimulate a robust T-cell–mediated immune response specifically targeting PSA-expressing prostate cancer cells. This approach aims to overcome immune tolerance and induce cytotoxic T lymphocyte activity against tumor cells. Clinical studies have demonstrated that this strategy can reliably induce PSA-specific T-cell responses in patients with metastatic or recurrent prostate cancer, with evidence of decreased serum PSA levels and transient clearance of circulating tumor cells in some cases[1][4]. The method is considered safe and feasible for clinical use[4].
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 prostate-specific antigen RNA-pulsed dendritic cell vaccine.