MVA-BN® PRO

Prostate cancer immunotherapy product candidate

Phase I/II

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MVA-BN® PRO is  is designed to express sequences that control immunity to PSA and Prostatic Acid Phosphatase (PAP). These highly prostate-specific antigens have shown promise as tumor targets when evaluated separately in clinical studies. PSA is the target of the PROSTVAC® immunotherapy program. The concomitant targeting of two prevalent antigens to treat prostate cancer is a distinctive feature of MVA-BN® PRO. It is anticipated that this feature will confer superior cancer vaccine efficacy and alleviate tumor immune evasion.

The dual vaccine properties of MVA-BN® PRO were verified in preclinical studies that showed induction of broad and comprehensive immune responses to both PSA and PAP following administration of MVA-BN® PRO.

Based on the positive preclinical evaluation of MVA-BN® PRO, a Phase I/II safety and tolerability study in 18 male patients with non-metastatic hormone-insensitive prostate cancer has begun in the US. Preliminary immune evaluation of T-cell responses have showed vaccine-induced responses to both PSA and PAP. Most importantly, treatment in this patient population also resulted in the induction of T-cell responses to tumor antigens other than PSA and PAP. These preliminary data are encouraging as it suggests that MVA-BN® PRO-induced anti-PSA and PAP responses may have led to tumoricidal activity.