Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
PROSTVAC V/F (rilimogene galvacirepvec) is a therapeutic cancer vaccine developed by Bavarian Nordic for the treatment of prostate cancer. It employs a heterologous prime-boost strategy using two different recombinant viral vectors: a vaccinia virus (PROSTVAC-V) for the initial priming dose and a fowlpox virus (PROSTVAC-F) for subsequent booster injections. Both vectors are engineered to express the prostate-specific antigen (PSA) with an L155 mutation to enhance T-cell recognition, along with a triad of human T-cell costimulatory molecules (B7.1, ICAM-1, and LFA-3), collectively known as TRICOM. The vaccine is designed to stimulate the immune system to recognize and destroy PSA-expressing prostate cancer cells. Although it demonstrated a survival benefit in Phase 2 trials, the pivotal Phase 3 PROSPECT trial in metastatic castration-resistant prostate cancer (mCRPC) failed to meet its primary endpoint of overall survival, leading to the discontinuation of its development for that specific indication as a monotherapy.
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 rilimogene galvacirepvec (Bavarian Nordic).