<HashMap><database>ecrin-mdr-crc</database><scores/><additional><omics_type>Clinical</omics_type><study_start_year>2006</study_start_year><condition>Previously untreated metastatic colorectal cancer</condition><disease>Previously Untreated Metastatic Colorectal Cancer</disease><study_type>Interventional</study_type><full_dataset_link>https://newmdr.ecrin.org/Study/2518837</full_dataset_link><location>United Kingdom</location><study_start_month>5</study_start_month><keyword>Xeloda</keyword><keyword>Mitomycin-C</keyword><keyword>Avastin</keyword><repository>ECRIN MDR</repository><study_status>Completed</study_status></additional><is_claimable>false</is_claimable><name>The MAX study: A randomised phase II/III study to evaluate the role of Mitomycin C, Avastin and Xeloda in patients with untreated metastatic colorectal cancer</name><description>Primary objectives: Phase II stagePrimary Objective:• To determine the relative toxicity of the combination of capecitabine andbevacizumab and the combination of capecitabine, mitomycin C (MMC) andbevacizumab with that of capecitabine monotherapy.
Phase III stagePrimary Objective:• To compare progression-free survival (PFS) on the three arms
Primary endpoints: Phase II stagePrimary Endpoint: Treatment-related toxicity
Phase III stagePrimary endpoint: Progression free survival (PFS)</description><dates><creation>2006-05-15</creation></dates><accession>2518837</accession><cross_references><EU Clinical Trials Register>2005-005761-11</EU Clinical Trials Register></cross_references></HashMap>