<HashMap><database>ecrin-mdr-crc</database><scores/><additional><omics_type>Clinical</omics_type><study_start_year>2022</study_start_year><data_sharing_plan>IPD Sharing (as of November 2023): No</data_sharing_plan><condition>Metastatic Colorectal Cancer</condition><condition>Colorectal Neoplasms</condition><disease>Metastatic Colorectal Cancer</disease><disease>Colorectal Neoplasms</disease><study_type>Interventional</study_type><full_dataset_link>https://newmdr.ecrin.org/Study/2718914</full_dataset_link><location>Canada</location><location>Puerto Rico</location><location>Belgium</location><location>Hong Kong</location><location>United States</location><location>Italy</location><location>France</location><location>Australia</location><location>Germany</location><location>Spain</location><study_start_month>7</study_start_month><keyword>Magrolimab</keyword><keyword>Irinotecan</keyword><keyword>Leucovorin</keyword><keyword>Fluorouracil</keyword><keyword>Bevacizumab</keyword><repository>ECRIN MDR</repository><study_status>Recruiting</study_status></additional><is_claimable>false</is_claimable><name>Study of Magrolimab Given Together With FOLFIRI/BEV in Patients With Previously Treated Advanced Inoperable Metastatic Colorectal Cancer (mCRC)</name><description>The goals of this clinical study are to learn more about the safety, tolerability and effectiveness of magrolimab in combination with bevacizumab and 5-fluorouracil, irinotecan, and leucovorin (FOLFIRI) in previously treated participants with advanced inoperable metastatic colorectal cancer (mCRC).
The primary objectives of this study are: (safety run-in cohort) to evaluate safety and tolerability, and the recommended Phase 2 dose (RP2D) and (randomized cohort) to evaluate the efficacy of magrolimab in combination with bevacizumab and 5-fluorouracil, irinotecan, and leucovorin (FOLFIRI) in previously treated participants with advanced inoperable metastatic colorectal cancer (mCRC).</description><dates><creation>2022-07-15</creation></dates><accession>2718914</accession><cross_references><ClinicalTrials___gov>NCT05330429</ClinicalTrials___gov><EU Clinical Trials Register>2022-500177-13</EU Clinical Trials Register></cross_references></HashMap>