Drug intelligence / Profile preview

Ad-PS2

Development stage
Preclinical
Lead developer
National Cancer Institute
Modality
Viral Vectors → Gene Addition/Replacement → Gene Therapies, Vaccines & Immunotherapeutics
Administration
Intramuscular, Subcutaneous
01

Overview

Ad-PS2 is an investigational bivalent adenoviral-vector-based vaccine designed for the treatment of prostate cancer. Developed by researchers at the National Cancer Institute (NCI), it utilizes an adenovirus platform to deliver two key prostate-associated tumor antigens: Prostate-Specific Antigen (PSA) and Prostate-Specific Membrane Antigen (PSMA). The vaccine is engineered to stimulate a robust, antigen-specific CD8+ T-cell immune response against malignant prostate cells. Preclinical studies have demonstrated that Ad-PS2 exhibits significant therapeutic synergy when combined with immune checkpoint inhibitors, particularly CTLA-4 blockade. This combination therapy has been shown to increase intratumoral CD8+ T-cell infiltration and establish durable immune protection against tumor rechallenge, suggesting a potential strategy to overcome immunotherapy resistance in prostate cancer patients.

Other names
Adenovirus-based bivalent prostate cancer vaccineAd5-PSA-PSMA vaccineAd-5-PSA-PSMA vaccineAd 5-PSA-PSMA vaccine
02

Targets

PSMA (Prostate-specific membrane antigen)PSA (Puromycin-sensitive aminopeptidase)

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