Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**PDS0101 + pembrolizumab** is a combination regimen comprising two agents: - **PDS0101**: A molecularly targeted immunotherapy formulated as an enantiospecific cationic lipid nanoparticle vaccine, containing synthetic peptides derived from HPV16 E6/E7 neoantigens. It is designed to induce robust, long-lasting, multifunctional HPV16-specific CD8 and CD4 T cell responses by upregulating Type I interferons, enhancing antigen processing and cross-presentation, and reversing immune evasion caused by HPV oncoproteins[1][3][4][6]. - **Pembrolizumab**: An intravenous monoclonal antibody checkpoint inhibitor that blocks PD-1 (programmed cell death protein 1) on T cells, thereby preventing tumor-induced immune suppression and enhancing antitumor T-cell activity. This combination aims to address recurrent or metastatic HPV16-positive head and neck squamous cell carcinoma (HNSCC), leveraging complementary immunologic mechanisms to improve patient survival and tumor response rates. PDS0101 is administered subcutaneously in several cycles combined with regular IV pembrolizumab infusions[1][2][3][4][6].
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 PDS0101 + pembrolizumab.