Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
ASP1012 + pembrolizumab is a combination of an investigational oncolytic immunotherapeutic virus (ASP1012) and an immune checkpoint inhibitor (pembrolizumab) under clinical investigation for patients with advanced or metastatic solid tumors. ASP1012 is a double-stranded DNA oncolytic vaccinia virus encoding a leptin-interleukin 2 fusion protein, designed for intravenous administration to selectively replicate in and destroy cancer cells, while enhancing anti-tumor immunity through its transgene payload. Pembrolizumab is a humanized monoclonal antibody targeting programmed cell death protein 1 (PD-1), blocking inhibitory signaling on T cells and thus promoting anti-tumor immune responses. This combination aims to synergistically kill tumor cells: ASP1012 directly lyses tumor cells and stimulates local immune activation, while pembrolizumab releases brakes on T cell immunity, with the goal of greater efficacy than either agent alone. Developed and sponsored by Astellas Pharma in collaboration with KaliVir Immunotherapeutics, the combination is currently under phase 1 clinical evaluation for solid tumors, including colorectal cancer, gastric cancer, melanoma, and ovarian cancer[2][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 ASP1012 + pembrolizumab.