Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
PR1 is a peptide-based cancer vaccine consisting of a 9-amino acid HLA-A2-restricted peptide (sequence: VLQELNVTV) derived from the leukemia-associated antigens proteinase 3 (PR3) and neutrophil elastase (NE). These proteins are primary granule proteins that are overexpressed in the blasts of patients with acute myeloid leukemia (AML) and chronic myeloid leukemia (CML). The vaccine is designed to stimulate a specific cytotoxic T-lymphocyte (CTL) response to target and eliminate residual leukemic cells. It is typically co-administered with sargramostim (GM-CSF), which serves as an immunological adjuvant to promote the recruitment and maturation of antigen-presenting cells at the injection site. Developed by The Vaccine Company, the PR1 vaccine reached Phase 3 clinical evaluation for maintaining remission in AML patients, although the pivotal trial was ultimately terminated.
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 PR1 peptide vaccine + sargramostim.