<HashMap><database>ecrin-mdr-crc</database><scores/><additional><omics_type>Clinical</omics_type><study_start_year>2016</study_start_year><data_sharing_plan>IPD Sharing (as of September 2020): No</data_sharing_plan><condition>C18-9</condition><condition>Metastatic Colorectal Cancer</condition><condition>Colorectal Neoplasms</condition><condition>Malignant neoplasm of colon</condition><disease>C18-9</disease><disease>Metastatic Colorectal Cancer</disease><disease>Colorectal Neoplasms</disease><disease>Malignant Neoplasm Of Colon</disease><study_type>Interventional</study_type><full_dataset_link>https://newmdr.ecrin.org/Study/2254808</full_dataset_link><location>Iran</location><location>Aland Islands</location><study_start_month>10</study_start_month><keyword>Irinotecan</keyword><keyword>Leucovorin</keyword><keyword>Fluorouracil</keyword><keyword>Bevacizumab</keyword><repository>ECRIN MDR</repository><study_status>Completed</study_status></additional><is_claimable>false</is_claimable><name>Comparing Efficacy and Safety of Stivant (AryoGen Bevacizumab) Versus Avastin in Metastatic Colorectal Cancer</name><description>This is a Phase III, randomized, two arms, double-blind (patient and assessor blinded), parallel active non inferiority controlled clinical trial with a 2:1 allocation. This trial was conducted to evaluate the efficacy and safety of bevacizumab (produced by AryoGen Pharmed) plus FOLFIRI-3 compared with bevacizumab (Avastin) plus FOLFIRI-3 in patients with metastatic colorectal cancer (mCRC). Patients who met the following criteria could be recruited to receive the mentioned intervention randomly. Inclusion criteria: male or female aged 18-75 years, mCRC verified histologically, Having one or more bi-dimensionally measurable lesions as defined by Response Evaluation Criteria In Solid Tumors (RECIST) criteria, Was not felt to be amenable to curative resection, With an (ECOG) performance status of ≤ 1, Life expectancy of longer than 3 months, Adequate organ and marrow function, May have received adjuvant therapy for primary colorectal cancer provided that at least 6 months have elapsed from the time the adjuvant therapy was concluded and recurrent disease was documented, Patients with history of hypertension must be well-controlled (blood pressure less than/equal to 150/100), on a stable regimen of anti-hypertensive therapy.</description><dates><creation>2016-10-15</creation></dates><accession>2254808</accession><cross_references><ClinicalTrials___gov>NCT03288987</ClinicalTrials___gov><Iranian Registry of Clinical Trials>IRCT2015072517994N2</Iranian Registry of Clinical Trials></cross_references></HashMap>