<HashMap><database>ecrin-mdr-crc</database><scores/><additional><omics_type>Clinical</omics_type><study_start_year>2008</study_start_year><condition>Rectal Neoplasms</condition><condition>Locally advanced rectal cancer</condition><condition>Colorectal Cancer</condition><disease>Rectal Neoplasms</disease><disease>Colorectal Cancer</disease><disease>Locally Advanced Rectal Cancer</disease><study_type>Interventional</study_type><full_dataset_link>https://newmdr.ecrin.org/Study/2064382</full_dataset_link><location>Slovakia</location><study_start_month>10</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) Plus Radiotherapy in Participants With Locally Advanced Rectal Cancer</name><description>This single arm study will assess the efficacy and safety of treatment with Xeloda plus standard pelvic radiotherapy in participants with locally advanced rectal cancer. Eligible participants will receive Xeloda 825mg/m^2 orally twice daily plus standard radiotherapy for 5 weeks, followed by surgery within 6 weeks after completion of treatment. The anticipated time on study treatment is &lt; 3 months, and the target sample size is &lt; 100 individuals.</description><dates><creation>2008-10-15</creation></dates><accession>2064382</accession><cross_references><ClinicalTrials___gov>NCT00796718</ClinicalTrials___gov><EU Clinical Trials Register>2008-003980-38</EU Clinical Trials Register></cross_references></HashMap>