<HashMap><database>ecrin-mdr-crc</database><scores/><additional><omics_type>Clinical</omics_type><study_start_year>2005</study_start_year><condition>Adenocarcinoma</condition><condition>Colorectal Cancer</condition><condition>Metastases</condition><disease>Adenocarcinoma</disease><disease>Colorectal Cancer</disease><disease>Metastases</disease><study_type>Interventional</study_type><full_dataset_link>https://newmdr.ecrin.org/Study/2012161</full_dataset_link><location>United States</location><study_start_month>1</study_start_month><keyword>Metastatic Colorectal Adenocarcinoma</keyword><keyword>Anti TAG-72</keyword><keyword>Monoclonal Antibody</keyword><repository>ECRIN MDR</repository><study_status>Terminated</study_status></additional><is_claimable>false</is_claimable><name>Safety and Activity of 90Y-Labeled IDEC-159 in Subjects With Metastatic Colorectal Adenocarcinoma</name><description>This is a Phase I/II open-label, dose-escalating study in patients with metastatic colorectal cancer. The objectives of the study are to obtain information on the safety of radiolabeled IDEC-159, as well as its activity in colorectal cancer. Another objective is to determine the maximum tolerated dose (MTD). The study duration is 2 years with visits occuring daily and/or weekly for the first 3 months, and every 6 weeks until the end of the 2 year period.</description><dates><creation>2005-01-15</creation></dates><accession>2012161</accession><cross_references><ClinicalTrials___gov>NCT00102024</ClinicalTrials___gov></cross_references></HashMap>