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Synthetic long peptide and DNA personalized cancer vaccines induce robust neoantigen-specific T cell responses in pancreatic cancer.

Felicia Zhang Perkins, Xiuli Zhang, Yik Yeung Lawrence Yu, Yilin Yang, Darren Cullinan, Kartik Singhal, Carlos A Parra-Lopez, Christopher A Miller, Binghan Yan, Julia W Angkeow, Jinglun Li, Nancy B Myers, Tammi Vickery, John Herndon, Rashmi Mishra, Stephanie Myles, Dominic Sanford, Elizabeth M Jaffee, Daniel A Laheru, Andrea Wang-Gillam, Marianna B Ruzinova, Ian S Hagemann, Sherri R Davies, Timothy P Fleming, Shelby Namen, Carl J DeSelm, Lijin Li, Roheena Z Panni, Feng Gao, Kian-Huat Lim, Obi L Griffith, Malachi Griffith, Robert D Schreiber, S Peter Goedegebuure, William G Hawkins, William E Gillanders

Science advancesSep 4, 2026PMID 42696575doi:10.1126/sciadv.aei1190 PMC13544235Journal ArticleClinical Trial, Phase IpubmedProvenance
Source
PubMed
Retrieved
Sep 10, 2026
Layer
normalized (units and labels harmonized; values unchanged)
Run
ING-PUBMED-20260910-000001
Published

Abstract

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Pancreatic ductal adenocarcinoma (PDAC) is unresponsive to standard immunotherapies despite harboring cancer neoantigens capable of eliciting T cell responses. We completed two phase 1 clinical trials (NCT03956056 and NCT03122106) evaluating safety and immunogenicity of synthetic long peptide (SLP)…

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Validated 2

Candidate 1

Registered trialsNCT03122106NCT03956056

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