<HashMap><database>ecrin-mdr-crc</database><scores/><additional><omics_type>Clinical</omics_type><study_start_year>2018</study_start_year><condition>Gastric Cancer</condition><condition>Colorectal Cancer</condition><condition>Esophageal Cancer</condition><condition>Cholangiocarcinoma</condition><condition>Hepatocellular Carcinoma</condition><disease>Gastric Cancer</disease><disease>Colorectal Cancer</disease><disease>Esophageal Cancer</disease><disease>Cholangiocarcinoma</disease><disease>Hepatocellular Carcinoma</disease><study_type>Interventional</study_type><full_dataset_link>https://newmdr.ecrin.org/Study/2289040</full_dataset_link><location>China</location><study_start_month>11</study_start_month><repository>ECRIN MDR</repository><study_status>Not provided</study_status></additional><is_claimable>false</is_claimable><name>A Phase 1 Study of ZSP1241 in Participants With Advanced Solid Tumors</name><description>The purpose of this study is to evaluate the safety, tolerability and pharmacokinetics, and determine the maximum tolerated dose of ZSP1241 in participants with hepatocellular carcinoma, cholangiocarcinoma, gastric cancer, esophageal cancer, colorectal cancer and other advanced solid tumors.</description><dates><creation>2018-11-15</creation></dates><accession>2289040</accession><cross_references><ClinicalTrials___gov>NCT03734926</ClinicalTrials___gov></cross_references></HashMap>