<HashMap><database>ecrin-mdr-crc</database><scores/><additional><omics_type>Clinical</omics_type><study_start_year>2018</study_start_year><data_sharing_plan>IPD Sharing (as of November 2020): No</data_sharing_plan><condition>Unresectable Metastatic Colorectal Cancer</condition><condition>Colorectal Neoplasms</condition><disease>Unresectable Metastatic Colorectal Cancer</disease><disease>Colorectal Neoplasms</disease><study_type>Interventional</study_type><full_dataset_link>https://newmdr.ecrin.org/Study/2285775</full_dataset_link><location>Belgium</location><location>United States</location><study_start_month>11</study_start_month><repository>ECRIN MDR</repository><study_status>Recruiting</study_status></additional><is_claimable>false</is_claimable><name>alloSHRINK - Standard cHemotherapy Regimen and Immunotherapy With Allogeneic NKG2D-based CYAD-101 Chimeric Antigen Receptor T-cells</name><description>The purpose of the alloSHRINK study is to assess the safety, cell kinetics and clinical activity of CYAD-101 in patients with unresectable metastatic colorectal cancer administered after standard chemotherapy</description><dates><creation>2018-11-15</creation></dates><accession>2285775</accession><cross_references><ClinicalTrials___gov>NCT03692429</ClinicalTrials___gov></cross_references></HashMap>