Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
INO-5401 + Libtayo is a combination immunotherapy regimen consisting of INO-5401, a synthetic DNA medicine, and cemiplimab (Libtayo), a programmed death receptor-1 (PD-1) blocking monoclonal antibody. INO-5401 is designed to activate the immune system against multiple tumor-associated antigens, including human telomerase reverse transcriptase (hTERT), Wilms tumor gene 1 (WT1), and prostate-specific membrane antigen (PSMA). Cemiplimab acts as a checkpoint inhibitor to prevent the PD-1/PD-L1 interaction, thereby enhancing T-cell mediated anti-tumor responses. This combination is primarily being investigated for the treatment of newly diagnosed glioblastoma (GBM) to improve survival outcomes by priming and sustaining a robust immune response against the tumor. The regimen often includes INO-9012, a DNA plasmid encoding interleukin-12 (IL-12), which serves as an immune booster.
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 INO-5401 + cemiplimab.