Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
PERVI-FUS is an investigational personalized peptide vaccine developed by the University Hospital Tübingen (Universitätsklinikum Tübingen) for the treatment of fusion-gene driven sarcomas, including Ewing sarcoma, alveolar rhabdomyosarcoma, and synovial sarcoma. The vaccine is designed to elicit a T-cell mediated immune response against tumor-specific neoantigens derived from the unique junction sequences of chromosomal translocation-induced fusion proteins, such as EWS-FLI1, PAX3-FOXO1, or SS18-SSX. By targeting these junction sequences, which are absent in healthy tissue, the therapy aims to provide a highly specific immunotherapy. The vaccine is typically formulated with the novel lipopeptide adjuvant XS15 (a TLR1/2 ligand) emulsified in Montanide ISA 51 VG to enhance the induction of cytotoxic CD8+ and helper CD4+ T cells. It is currently being evaluated in Phase 1 clinical trials to assess safety and immunogenicity in patients with refractory or high-risk sarcomas.
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 PERVI-FUS.