<HashMap><database>ecrin-mdr-crc</database><scores/><additional><omics_type>Clinical</omics_type><study_start_year>2005</study_start_year><condition></condition><condition>Histologically confirmed adenocarcinoma of the colon or the rectum and unresectable metastases or advanced locoregional disease</condition><disease></disease><disease>Histologically Confirmed Adenocarcinoma Of The Colon Or The Rectum And Unresectable Metastases Or Advanced Locoregional Disease</disease><study_type>Interventional</study_type><full_dataset_link>https://newmdr.ecrin.org/Study/2516699</full_dataset_link><location>Belgium</location><study_start_month>5</study_start_month><keyword>ELVORINE, 50mg/5ml, solution for injection</keyword><keyword>Vorina®, 350mg/14ml, solution for injection</keyword><keyword>FLURACEDYL, 1000mg/20ml, solution for injection; 5000mg/100ml solution for injection</keyword><keyword>Rescuvolin®, 300mg/12ml, solution for injection</keyword><repository>ECRIN MDR</repository><study_status>Completed</study_status></additional><is_claimable>false</is_claimable><name>SFOLFOX/SFOLFIRI vs FOLFOX/FOLFIRI</name><description>Primary objectives: The first objective is to evaluate, in terms of Objective Response Rate (ORR), whether the combined infusional Leucovorin Sodium and 5-FU has the potential of being superior to the standard sequential administration of Leucovorin Calcium and 5-FU, both in combination with standard Irinotecan or Oxaliplatin.
Primary endpoints: The primary end-point for efficacy is the Objective Response Rate (using RECIST criteria) during the treatment period.</description><dates><creation>2005-05-15</creation></dates><accession>2516699</accession><cross_references><EU Clinical Trials Register>2004-004901-12</EU Clinical Trials Register></cross_references></HashMap>