<HashMap><database>ecrin-mdr-crc</database><scores/><additional><omics_type>Clinical</omics_type><study_start_year>2005</study_start_year><condition>Colorectal Cancer</condition><condition>Colorectal Neoplasms</condition><disease>Colorectal Cancer</disease><disease>Colorectal Neoplasms</disease><study_type>Interventional</study_type><full_dataset_link>https://newmdr.ecrin.org/Study/2200534</full_dataset_link><location>Bulgaria</location><study_start_month>8</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 Capecitabine (Xeloda) in the Adjuvant Treatment of Participants With Resected Colon Cancer</name><description>This study will evaluate the safety and tolerability of capecitabine (Xeloda) in participants who have undergone surgery for colon cancer. Oral Xeloda will be administered twice daily in 3-week cycles for a total of up to 8 cycles. The anticipated time on study treatment is 24 weeks, and the target sample size is 70 individuals.</description><dates><creation>2005-08-15</creation></dates><accession>2200534</accession><cross_references><ClinicalTrials___gov>NCT02581423</ClinicalTrials___gov></cross_references></HashMap>