<HashMap><database>ecrin-mdr-crc</database><scores/><additional><omics_type>Clinical</omics_type><study_start_year>2010</study_start_year><data_sharing_plan>IPD Sharing (as of October 2019): No</data_sharing_plan><condition>Colorectal cancer metastatic</condition><condition>Colorectal Cancer</condition><condition>Colorectal Neoplasms</condition><condition>K-Ras wild type metastatic colorectal cancer</condition><disease>K-ras Wild Type Metastatic Colorectal Cancer</disease><disease>Colorectal Cancer</disease><disease>Colorectal Neoplasms</disease><disease>Colorectal Cancer Metastatic</disease><study_type>Interventional</study_type><full_dataset_link>https://newmdr.ecrin.org/Study/2098880</full_dataset_link><location>Austria</location><location>Belgium</location><location>Hungary</location><location>France</location><location>Spain</location><study_start_month>12</study_start_month><keyword>Standard cetuximab + FOLFIRI</keyword><keyword>First line metastatic</keyword><keyword>K-Ras wildtype</keyword><keyword>Erbitux 5 mg/ml solution for infusion</keyword><keyword>Cetuximab</keyword><keyword>Dose escalation cetuximab</keyword><repository>ECRIN MDR</repository><study_status>Completed</study_status></additional><is_claimable>false</is_claimable><name>Cetuximab Standard or Dose Escalation in First Line Colorectal Cancer</name><description>The purposes of this study are to determine whether administering escalating doses of cetuximab in patients with no early skin toxicity could delay the progression of disease in a significant proportion of patients and to study the molecular signatures of response.</description><dates><creation>2010-12-15</creation></dates><accession>2098880</accession><cross_references><ClinicalTrials___gov>NCT01251536</ClinicalTrials___gov><EU Clinical Trials Register>2009-009992-36</EU Clinical Trials Register></cross_references></HashMap>