<HashMap><database>ecrin-mdr-crc</database><scores/><additional><omics_type>Clinical</omics_type><study_start_year>2022</study_start_year><data_sharing_plan>IPD Sharing (as of April 2023): No</data_sharing_plan><condition>Colorectal Neoplasms</condition><disease>Colorectal Neoplasms</disease><study_type>Interventional</study_type><full_dataset_link>https://newmdr.ecrin.org/Study/2397135</full_dataset_link><location>United States</location><study_start_month>2</study_start_month><keyword>Individualized cancer vaccine</keyword><keyword>MCRC</keyword><keyword>Colorectal cancer vaccine</keyword><keyword>Rectal</keyword><keyword>Personalized cancer vaccine</keyword><keyword>Ipilimumab</keyword><keyword>Leucovorin</keyword><keyword>Bevacizumab</keyword><keyword>Personal cancer vaccine</keyword><keyword>CRC</keyword><keyword>Immunotherapy</keyword><keyword>Rectum</keyword><keyword>Colon</keyword><keyword>MSS-CRC</keyword><keyword>Atezolizumab</keyword><repository>ECRIN MDR</repository><study_status>Active, not recruiting</study_status></additional><is_claimable>false</is_claimable><name>A Study of a Patient-Specific Neoantigen Vaccine in Combination With Immune Checkpoint Blockade for Patients With Metastatic Colorectal Cancer</name><description>The primary objective of the Phase 2 portion of the study is to characterize the clinical activity of maintenance therapy with GRT-C901/GRT-R902 (patient-specific vaccines) in combination with checkpoint inhibitors in addition to fluoropyrimidine/bevacizumab versus a fluoropyrimidine/bevacizumab alone as assessed by molecular response which is based on changes in circulating tumor (ct)DNA. The primary objective of the Phase 3 portion is to demonstrate clinical efficacy of the regimen as assessed by progression-free survival.</description><dates><creation>2022-02-15</creation></dates><accession>2397135</accession><cross_references><ClinicalTrials___gov>NCT05141721</ClinicalTrials___gov></cross_references></HashMap>