<HashMap><database>ecrin-mdr-crc</database><scores/><additional><omics_type>Clinical</omics_type><study_start_year>2009</study_start_year><condition>Metastatic Colorectal Cancer</condition><condition>Colorectal cancer metastatic</condition><condition>Patients with chemotherapy-refractory metastatic colorectal cancer</condition><condition>Colorectal Neoplasms</condition><condition>Cancer</condition><disease>Metastatic Colorectal Cancer</disease><disease>Patients With Chemotherapy-refractory Metastatic Colorectal Cancer</disease><disease>Colorectal Cancer Metastatic</disease><disease>Colorectal Neoplasms</disease><disease>Cancer</disease><study_type>Interventional</study_type><full_dataset_link>https://newmdr.ecrin.org/Study/2074647</full_dataset_link><location>Austria</location><location>Germany</location><study_start_month>7</study_start_month><keyword>Cytavis</keyword><keyword>CY-503</keyword><keyword>Colorectal</keyword><keyword>Aviscumine</keyword><keyword>Phase II</keyword><keyword>Metastatic</keyword><keyword>Double-blind</keyword><keyword>Randomised</keyword><keyword>Multicenter</keyword><keyword>Controlled</keyword><repository>ECRIN MDR</repository><study_status>Terminated</study_status></additional><is_claimable>false</is_claimable><name>CY-503 for the Treatment of Chemotherapy-refractory Metastatic Colorectal Cancer</name><description>This trial is designed as a phase II evaluation of the effect of CY-503 or placebo on progression free survival (PFS) defined as the time from start of treatment until the objective observation of progressive disease (PD) or death from any course in patients with chemotherapy-refractory metastatic colorectal cancer.</description><dates><creation>2009-07-15</creation></dates><accession>2074647</accession><cross_references><ClinicalTrials___gov>NCT00932724</ClinicalTrials___gov><EU Clinical Trials Register>2008-005536-32</EU Clinical Trials Register></cross_references></HashMap>