<HashMap><database>ecrin-mdr-crc</database><scores/><additional><omics_type>Clinical</omics_type><study_start_year>2007</study_start_year><condition>Colorectal Cancer</condition><condition>Colonic Neoplasms</condition><disease>Colorectal Cancer</disease><disease>Colonic Neoplasms</disease><study_type>Interventional</study_type><full_dataset_link>https://newmdr.ecrin.org/Study/2042187</full_dataset_link><location>Russia</location><study_start_month>7</study_start_month><keyword>Capecitabine</keyword><repository>ECRIN MDR</repository><study_status>Completed</study_status></additional><is_claimable>false</is_claimable><name>A Study of Xeloda (Capecitabine) as Adjuvant Monotherapy in Patients With Colon Cancer.</name><description>This single arm study will evaluate the safety profile of Xeloda as monotherapy for adjuvant treatment of colon cancer. All patients will receive Xeloda 1250mg/m2 p.o. twice daily as intermittent treatment (3 week cycles consisting of 2 weeks of treatment followed by 1 week without treatment). The anticipated time on study treatment is 3-12 months, and the target sample size is 500+ individuals.</description><dates><creation>2007-07-15</creation></dates><accession>2042187</accession><cross_references><ClinicalTrials___gov>NCT00502671</ClinicalTrials___gov></cross_references></HashMap>