Drug intelligence / Profile preview

P30-EPS

Development stage
Phase 1
Lead developer
Duke University
Modality
Peptides, Vaccines & Immunotherapeutics
Administration
Intramuscular
01

Overview

**P30-EPS** is an investigational multipeptide therapeutic cancer vaccine developed at Duke University for newly diagnosed, MGMT-unmethylated glioblastoma. It combines HLA-A*02:01-restricted peptide antigens derived from ephrin type-A receptor 2, cytomegalovirus pp65, and survivin with the tetanus-toxoid-derived universal CD4+ helper epitope P30. The vaccine is intended to enhance coordinated CD4+ helper and CD8+ cytotoxic T-cell responses against glioblastoma-associated antigens and has been evaluated by intramuscular administration with the poly-ICLC adjuvant Hiltonol in the phase 1b ETAPA I trial. ([clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05283109))

Other names
P30-EPSP-30-EPSP 30-EPSP30-EPS vaccineP-30-EPS vaccineP 30-EPS vaccineP30-linked EphA2, CMV pp65, and survivin peptide vaccine
02

Targets

BIRC5 (Survivin)TCR-P30 (T-cell receptor recognizing the P30 tetanus toxin epitope)EPHA2 (Ephrin type-A receptor 2)pp65 (Cytomegalovirus phosphoprotein 65)HLA-A*02 (Human leukocyte antigen A*02 complexed peptide)

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