<HashMap><database>ecrin-mdr-crc</database><scores/><additional><omics_type>Clinical</omics_type><study_start_year>2005</study_start_year><condition>Colorectal Neoplasms</condition><condition>Neoplasms</condition><disease>Colorectal Neoplasms</disease><disease>Neoplasms</disease><study_type>Interventional</study_type><full_dataset_link>https://newmdr.ecrin.org/Study/2049493</full_dataset_link><location>United States</location><study_start_month>9</study_start_month><keyword>Sunitinib</keyword><keyword>Oxaliplatin</keyword><keyword>Colorectal cancer,</keyword><keyword>Advanced solid tumors,</keyword><keyword>Sunitinib (SUTENT),</keyword><keyword>Leucovorin</keyword><keyword>FOLFOX</keyword><keyword>Fluorouracil</keyword><repository>ECRIN MDR</repository><study_status>Completed</study_status></additional><is_claimable>false</is_claimable><name>Study Of Sunitinib Plus FOLFOX In Patients With Solid Tumors</name><description>This study determined the maximum tolerated dose and safety of SU011248 (sunitinib malate, SUTENT) in combination with FOLFOX [Leucovorin + Fluorouracil (5-FU) + Oxaliplatin]. Three different dosing regimens with starting doses of sunitinib at 37.5 mg/day (Schedule 2/2, Schedule 4/2, and Continuous Dosing) were tested in patients with advanced solid tumors, including colorectal cancer.</description><dates><creation>2005-09-15</creation></dates><accession>2049493</accession><cross_references><ClinicalTrials___gov>NCT00599924</ClinicalTrials___gov></cross_references></HashMap>