<HashMap><database>ecrin-mdr-crc</database><scores/><additional><omics_type>Clinical</omics_type><study_start_year>2002</study_start_year><condition>Diarrhea</condition><condition>Colorectal Neoplasms</condition><disease>Diarrhea</disease><disease>Colorectal Neoplasms</disease><study_type>Interventional</study_type><full_dataset_link>https://newmdr.ecrin.org/Study/2007577</full_dataset_link><location>United States</location><study_start_month>2</study_start_month><keyword>Concomitant use</keyword><keyword>CPT-11</keyword><keyword>Oral administration</keyword><keyword>Saltz regimen</keyword><keyword>Leucovorin</keyword><keyword>LV</keyword><keyword>Traditional chinese medicine</keyword><keyword>Reduce</keyword><keyword>Modulate</keyword><keyword>5-fluorouracil</keyword><keyword>Herbal medicine</keyword><keyword>Irinotecan</keyword><keyword>Oral dose</keyword><keyword>Chemotherapy</keyword><keyword>Alleviate</keyword><keyword>Stage III and Stage IV colorectal cancer</keyword><keyword>Botanical drug</keyword><keyword>Chinese herbal medicine</keyword><keyword>5-FU</keyword><keyword>Camptosar</keyword><keyword>Side effect</keyword><keyword>TCM</keyword><repository>ECRIN MDR</repository><study_status>Terminated</study_status></additional><is_claimable>false</is_claimable><name>Safety Study of the Chemotherapy Modulator PHY906 in Patients With Advanced Colorectal Cancer</name><description>The triple combination chemotherapy of irinotecan, 5-fluorouracil and leucovorin (CPT-11/5-FU/LV or Saltz regimen) is the treatment of choice for patients with advanced colorectal cancer. Severe diarrhea, unfortunately, is a side effect of such treatment. Preclinical studies have indicated that the botanical drug PHY906 can reduce such diarrhea without compromising the effectiveness of the chemotherapy. The primary purpose of this clinical study is to evaluate the safety, tolerability and minimum effective dose of PHY906 when administered in conjunction with the Saltz regimen.</description><dates><creation>2002-02-15</creation></dates><accession>2007577</accession><cross_references><ClinicalTrials___gov>NCT00036517</ClinicalTrials___gov></cross_references></HashMap>