<HashMap><database>ecrin-mdr-crc</database><scores/><additional><omics_type>Clinical</omics_type><study_start_year>2006</study_start_year><condition>Rectum Cancer</condition><condition>Rectal Neoplasms</condition><condition>Colorectal cancer</condition><disease>Rectum Cancer</disease><disease>Rectal Neoplasms</disease><disease>Colorectal Cancer</disease><study_type>Interventional</study_type><full_dataset_link>https://newmdr.ecrin.org/Study/2035218</full_dataset_link><location>Netherlands</location><study_start_month>9</study_start_month><keyword>M-tor inhibitor</keyword><keyword>Sirolimus</keyword><keyword>Rapamycin</keyword><repository>ECRIN MDR</repository><study_status>Completed</study_status></additional><is_claimable>false</is_claimable><name>Safety Study of Rapamycin Administered Before and During Radiotherapy to Treat Rectum Cancer</name><description>Investigating the safety and the activity of Rapamycin, administered before and during preoperative radiotherapy in patients with an operable colorectal carcinoma. The phase I dose escalation study will be performed in three steps (2, 4 and 6 mg). Patients entered in phase II will follow the same tolerable treatment regimen as patients in phase I study.</description><dates><creation>2006-09-15</creation></dates><accession>2035218</accession><cross_references><ClinicalTrials___gov>NCT00409994</ClinicalTrials___gov></cross_references></HashMap>