Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**TAS0313** is a novel cancer peptide vaccine cocktail under clinical development for the treatment of solid tumors, including glioblastoma and urothelial carcinoma. It comprises three long peptides (TAS0314, TAS0315, TAS0316), collectively presenting 12 cytotoxic T lymphocyte (CTL) epitope peptides restricted by multiple HLA types (A2, A24, A3-supertypes). These peptides are derived from eight cancer-associated antigens frequently expressed in tumors: squamous cell carcinoma antigen recognized by T-cells 2 (SART2), SART3, multidrug resistance-associated protein 3 (MRP3), epidermal growth factor receptor (EGFR), Wolf-Hirschhorn syndrome candidate 2 protein (WHSC2), transmembrane protein 189 (TMEM189), tyrosine-protein kinase LCK, and parathyroid hormone-related protein (PTHRP). By stimulating both cellular (CTLs) and humoral (IgG) immune responses, TAS0313 is intended to enhance antitumor immunity. Clinical trials have confirmed its safety, tolerability, and immunogenicity in patients with advanced solid tumors. Trials evaluating its efficacy both as monotherapy and combined with pembrolizumab are ongoing[1][2][3][4][5][7][8].
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 TAS0313.