<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>Cáncer colorrectal metastásico no pretratado</condition><condition>Colorectal Neoplasms</condition><condition>Colorectal cancer NOS</condition><disease>Metastatic Colorectal Cancer</disease><disease>Cáncer Colorrectal Metastásico No Pretratado</disease><disease>Colorectal Neoplasms</disease><disease>Colorectal Cancer Nos</disease><study_type>Interventional</study_type><full_dataset_link>https://newmdr.ecrin.org/Study/2070371</full_dataset_link><location>Spain</location><study_start_month>4</study_start_month><keyword>Irinotecan</keyword><keyword>Xeloda 150mg.</keyword><keyword>Avastin 400mg.</keyword><keyword>Capecitabine</keyword><keyword>Xeloda 500mg.</keyword><keyword>Avastin 100mg.</keyword><keyword>Bevacizumab</keyword><repository>ECRIN MDR</repository><study_status>Completed</study_status></additional><is_claimable>false</is_claimable><name>Irinotecan, Capecitabine and Bevacizumab in Metastatic Colorectal Cancer Patients</name><description>The purpose of this study is to determine efficacy and safety of the biweekly scheme with Capecitabine and Irinotecan, plus bevacizumab in patients with metastatic colorectal cancer.</description><dates><creation>2009-04-15</creation></dates><accession>2070371</accession><cross_references><ClinicalTrials___gov>NCT00875771</ClinicalTrials___gov><EU Clinical Trials Register>2008-004688-20</EU Clinical Trials Register></cross_references></HashMap>