Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
S-488211 is an investigational cancer peptide vaccine developed for the treatment of solid tumors, including non-muscle invasive bladder cancer. It is a freeze-dried injectable formulation containing two peptides—S-488204 (derived from DEPDC1) and S-488205 (derived from MPHOSPH1)—which are human leukocyte antigen (HLA)-A*02:01-restricted epitope peptides derived from cancer-testis antigens. These antigens are highly and differentially expressed in various solid tumors. The vaccine is designed to stimulate the immune system by presenting these tumor-associated antigens to antigen-presenting cells, leading to activation of cytotoxic T lymphocytes that target and destroy tumor cells[1][5]. S-488211 has been studied in combination with durvalumab, a PD-L1 inhibitor, in phase 1/2 clinical trials for non-muscle invasive bladder cancer[2][4][7].
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 S-488211.