<HashMap><database>ecrin-mdr-crc</database><scores/><additional><omics_type>Clinical</omics_type><study_start_year>2014</study_start_year><data_sharing_plan>IPD Sharing (as of February 2019): No</data_sharing_plan><condition>Colorectal Cancer</condition><condition>Head and Neck Cancer</condition><condition>Head and Neck Neoplasms</condition><disease>Colorectal Cancer</disease><disease>Head And Neck Neoplasms</disease><disease>Head And Neck Cancer</disease><study_type>Interventional</study_type><full_dataset_link>https://newmdr.ecrin.org/Study/2146162</full_dataset_link><location>United States</location><study_start_month>5</study_start_month><keyword>Nilotinib</keyword><keyword>Squamous cell carcinoma</keyword><keyword>Metastatic Kras wildtype</keyword><keyword>Cetuximab</keyword><repository>ECRIN MDR</repository><study_status>Terminated</study_status></additional><is_claimable>false</is_claimable><name>A Phase I Study of Nilontinib and Cetuximab in Patients With Solid Tumors</name><description>The purpose of this study is to determine the recommended Phase II dose of nilotinib when used in combination with cetuximab in the treatment of patients with recurrent and/or metastatic Kras wildtype colorectal cancer or squamous cell carcinoma of the head and neck.</description><dates><creation>2014-05-15</creation></dates><accession>2146162</accession><cross_references><ClinicalTrials___gov>NCT01871311</ClinicalTrials___gov></cross_references></HashMap>