Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Neoantigen vaccine + anti-PD1 + chemotherapy refers to an investigational combination regimen being evaluated as an adjuvant treatment for resected pancreatic ductal adenocarcinoma (PDAC). In the specific context of clinical trial NCT06344156, the regimen consists of a personalized neoantigen vaccine (referred to as Neovax), the anti-PD-1 monoclonal antibody tislelizumab (Tevimbra), and a chemotherapy backbone of gemcitabine and capecitabine (GemCap). The personalized vaccine is designed to stimulate a T-cell response against patient-specific tumor mutations, while tislelizumab prevents immune evasion by blocking the PD-1/PD-L1 pathway. The chemotherapy component serves to eliminate residual disease and potentially enhance the immunogenicity of the tumor. This multi-modal approach aims to improve recurrence-free survival in patients with high-risk resected pancreatic cancer.
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 neoantigen vaccine + tislelizumab + gemcitabine + capecitabine.