<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>91</volume><submitter>Wijaya W</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Survivin, an inhibitor of apoptosis protein (IAP), is highly expressed in various cancers but has weak immunogenicity as a self-derived tumour-associated antigen (TAA). OVM-200, a survivin recombinant overlapping peptide (ROP) vaccine, consists of overlapping peptides linked by the target sequence (LRMK) for cathepsin S, preserving T-cell and most antibody epitopes. OVM-200 elicits both cellular and humoral immune responses against survivin-expressing cancer cells. This phase 1a, multicentre, open-label trial (OVM-200-100) evaluates OVM-200 as a therapeutic vaccine in patients with non-small cell lung, ovarian, and prostate cancer. This Phase 1 trial is also the first time the ROP technology platform has been used in human trials.&lt;h4>Methods&lt;/h4>Twelve eligible patients </pubmed_abstract><journal>EClinicalMedicine</journal><pagination>103717</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12796589</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Survivin recombinant overlapping peptide (ROP) vaccine in advanced solid tumours: a first-in-human, multicentre, open-label, phase 1a dose-escalation study.</pubmed_title><pmcid>PMC12796589</pmcid><pubmed_authors>Tuthill M</pubmed_authors><pubmed_authors>Lu W</pubmed_authors><pubmed_authors>Forster MD</pubmed_authors><pubmed_authors>Finch W</pubmed_authors><pubmed_authors>Jiang S</pubmed_authors><pubmed_authors>Flynn M</pubmed_authors><pubmed_authors>Williams A</pubmed_authors><pubmed_authors>Wijaya W</pubmed_authors><pubmed_authors>Morris T</pubmed_authors><pubmed_authors>Thistlethwaite F</pubmed_authors></additional><is_claimable>false</is_claimable><name>Survivin recombinant overlapping peptide (ROP) vaccine in advanced solid tumours: a first-in-human, multicentre, open-label, phase 1a dose-escalation study.</name><description>&lt;h4>Background&lt;/h4>Survivin, an inhibitor of apoptosis protein (IAP), is highly expressed in various cancers but has weak immunogenicity as a self-derived tumour-associated antigen (TAA). OVM-200, a survivin recombinant overlapping peptide (ROP) vaccine, consists of overlapping peptides linked by the target sequence (LRMK) for cathepsin S, preserving T-cell and most antibody epitopes. OVM-200 elicits both cellular and humoral immune responses against survivin-expressing cancer cells. This phase 1a, multicentre, open-label trial (OVM-200-100) evaluates OVM-200 as a therapeutic vaccine in patients with non-small cell lung, ovarian, and prostate cancer. This Phase 1 trial is also the first time the ROP technology platform has been used in human trials.&lt;h4>Methods&lt;/h4>Twelve eligible patients </description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Jan</publication><modification>2026-06-09T05:36:08.34Z</modification><creation>2026-06-09T03:07:47.425Z</creation></dates><accession>S-EPMC12796589</accession><cross_references><pubmed>41536940</pubmed><doi>10.1016/j.eclinm.2025.103717</doi></cross_references></HashMap>