Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This combination therapy consists of the immune checkpoint inhibitor pembrolizumab (Keytruda) and the p53-specific synthetic long peptide (p53-SLP) vaccine. Pembrolizumab is a humanized monoclonal antibody that targets the programmed cell death protein 1 (PD-1) receptor, blocking its interaction with PD-L1 and PD-L2 to enhance T-cell mediated anti-tumor activity. The p53-SLP vaccine consists of 10 overlapping synthetic long peptides (averaging 30 amino acids in length) covering the core of the p53 protein from amino acids 70 to 251. It is formulated with the adjuvant Montanide ISA 51 to induce p53-specific T-cell responses. The combination is being investigated by the University Medical Center Groningen (UMCG) for the treatment of recurrent platinum-resistant ovarian cancer, aiming to overcome the immunosuppressive tumor microenvironment and boost the efficacy of vaccine-induced T-cells.
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 pembrolizumab + p53-SLP vaccine.