<HashMap><database>ecrin-mdr-crc</database><scores/><additional><omics_type>Clinical</omics_type><study_start_year>2018</study_start_year><data_sharing_plan>IPD Sharing (as of April 2023): Undecided</data_sharing_plan><condition>Malignant neoplasm of colon, Malignant neoplasm of rectum</condition><condition>Metastatic Colorectal Cancer</condition><condition>Colorectal Neoplasms</condition><condition>C18.9, C20</condition><condition>RAS wild-type Metastatic Colorectal Cancer</condition><disease>Metastatic Colorectal Cancer</disease><disease>Malignant Neoplasm Of Colon, Malignant Neoplasm Of Rectum</disease><disease>Colorectal Neoplasms</disease><disease>C18.9, C20</disease><disease>Ras Wild-type Metastatic Colorectal Cancer</disease><study_type>Interventional</study_type><full_dataset_link>https://newmdr.ecrin.org/Study/2262710</full_dataset_link><location>Iran</location><study_start_month>1</study_start_month><keyword>Irinotecan</keyword><keyword>Leucovorin</keyword><keyword>RAS Wild-type</keyword><keyword>Cetuximab</keyword><keyword>Fluorouracil</keyword><repository>ECRIN MDR</repository><study_status>Recruiting</study_status></additional><is_claimable>false</is_claimable><name>Comparing Efficacy and Safety of Cetuximab (CinnaGen) Versus Erbitux (Merck) in Metastatic Colorectal Cancer</name><description>The study is designed as phase III, randomized, two armed, parallel, double blind (patient and assessor blinded), active controlled, and equivalency clinical trial with primary endpoint of Progression-Free Survival of Cetuximab (produced by CinnaGen) compared with Erbitux (Cetuximab, the reference drug) in patients with RAS wild-type Metastatic Colorectal Cancer with the allocation ratio of 2:1.Patients who met the following criteria could be recruited to receive the mentioned intervention randomly. Inclusion criteria: Male or female older than 18 years old, histologically confirmed adenocarcinoma of the colon or rectum which is metastatic, having one or more bi-dimensionally measurable lesions as defined by RECIST criteria, tumor that could not be resected for curative purposes,ECOG performance status score of 2 or less,life expectancy of longer than 3 months (clinical assessment),evidence of tumor EGFR expression (expanded wild-type RAS),adequate organ and marrow function as defined:
ANC ≥ 1,500/mm3 Plt ≥ 100,000/mm3 Hb ≥ 9 g/dL (may have had blood transfusions) AST/ALT ≤ 2.5 IULN or ≤ 5 IULN with known liver metastases Total bilirubin ≤ 1.5 IULN Serum Creatinine ≤ 1.5 IULN INR ≤ 1.5 and PTT ≤ 1.5 IULN</description><dates><creation>2018-01-15</creation></dates><accession>2262710</accession><cross_references><ClinicalTrials___gov>NCT03391934</ClinicalTrials___gov><Iranian Registry of Clinical Trials>IRCT2017110821315N10</Iranian Registry of Clinical Trials></cross_references></HashMap>