Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**PERCELLVAC-Sur** is an autologous dendritic cell (DC) vaccine therapy loaded with Survivin tumor-associated antigens (TAAs) for immunotherapy in glioblastoma (GBM). It involves ex vivo loading of patient-derived DCs with Survivin peptides, followed by intradermal and intravenous administration to elicit anti-tumor T-cell responses. Developed for newly diagnosed GBM post-resection, chemoradiotherapy (radiotherapy + temozolomide), and adjuvant temozolomide, it is administered in three doses on days 0, 14, and 28 (dose escalation: 1\u00d710^7, 2\u00d710^7, or 3\u00d710^7 DCs; 1 ml intradermal + 5 ml IV). The therapy targets Survivin-expressing GBM to enhance immunogenicity and survival, with ongoing evaluation of safety, tolerability, PFS, OS, and immune responses in phase I/II trials.[3][4]
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 PERCELLVAC-Sur.