<HashMap><database>ecrin-mdr-crc</database><scores/><additional><omics_type>Clinical</omics_type><study_start_year>2015</study_start_year><condition>Colon Cancer</condition><condition>Colorectal Neoplasms</condition><disease>Colon Cancer</disease><disease>Colorectal Neoplasms</disease><study_type>Interventional</study_type><full_dataset_link>https://newmdr.ecrin.org/Study/2186793</full_dataset_link><location>United States</location><study_start_month>2</study_start_month><repository>ECRIN MDR</repository><study_status>Terminated</study_status></additional><is_claimable>false</is_claimable><name>A Biomarker Study in Patients Getting Regorafenib for Metastatic Colorectal Cancer</name><description>This is an exploratory biomarker study. Patients with metastatic colorectal cancer will receive regorafenib, which is FDA approved in this setting, on day 1-21 of every consecutive 28 day cycle. Patients will be asked to undergo tumor biopsy at baseline and 2 weeks after starting regorafenib. Peripheral blood samples will be collected at baseline 2 weeks after starting regorafenib, after initiation of cycle 3, and every 4 weeks thereafter.</description><dates><creation>2015-02-15</creation></dates><accession>2186793</accession><cross_references><ClinicalTrials___gov>NCT02402036</ClinicalTrials___gov></cross_references></HashMap>