<HashMap><database>ecrin-mdr-crc</database><scores/><additional><omics_type>Clinical</omics_type><study_start_year>2023</study_start_year><data_sharing_plan>IPD Sharing (as of October 2023): No</data_sharing_plan><condition>Pancreatic cancer</condition><condition>Colorectal cancer</condition><condition>Advanced Solid Tumor</condition><condition>Neoplasms</condition><disease>Colorectal Cancer</disease><disease>Advanced Solid Tumor</disease><disease>Pancreatic Cancer</disease><disease>Neoplasms</disease><study_type>Interventional</study_type><full_dataset_link>https://newmdr.ecrin.org/Study/114258</full_dataset_link><location>China</location><study_start_month>11</study_start_month><keyword>NKG2A</keyword><keyword>Urothelial carcinoma</keyword><keyword>Humanized monoclonal antibody</keyword><repository>ECRIN MDR</repository><study_status>Not yet recruiting</study_status></additional><is_claimable>false</is_claimable><name>A Study of HY-0102 in Patients With Advanced Solid Tumors</name><description>This is a phase 1 open label multicenter study to evaluate the maximum tolerance, safety, tolerance and PK of HY-0102 administered intravenously (IV) once every two weeks in patients with advanced solid tumors, so as to confirm the recommended phase 2 dose of HY-0102 and obtain the preliminary efficacy information of patients with advanced solid tumors.</description><dates><creation>2023-11-15</creation></dates><accession>114258</accession><cross_references><ClinicalTrials___gov>NCT06094777</ClinicalTrials___gov></cross_references></HashMap>