Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
The IPX vaccine is an individualized peptide-based immunotherapy developed by the University Hospital Tuebingen for the treatment of pediatric and young adult patients with metastatic fusion-driven sarcomas, specifically Ewing sarcoma, rhabdomyosarcoma, and synovial sarcoma. The vaccine is personalized for each patient, incorporating two primary peptide components: PERVI-NEO, which is derived from patient-specific nonsynonymous mutations identified via whole exome and RNA sequencing, and PERVI-FUS, which targets the unique fusion-breakpoint sequence characteristic of the patient's tumor. Additionally, a control peptide derived from Survivin is included. The vaccine is formulated with the novel Toll-like receptor (TLR) 1/2 ligand adjuvant XS15 and emulsified in Montanide ISA 51 VG to enhance the induction of tumor-specific T-cell responses. It is currently being evaluated in the Phase I/II PerVision clinical trial to assess safety and immunogenicity in patients who have achieved a clinical response following standard chemotherapy.
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 IPX vaccine.