<HashMap><database>ecrin-mdr-crc</database><scores/><additional><omics_type>Clinical</omics_type><study_start_year>2014</study_start_year><data_sharing_plan>IPD Sharing (as of November 2018): No</data_sharing_plan><condition>Ovarian Cancer</condition><condition>HepatoCellular Carcinoma</condition><condition>Lung Cancer</condition><condition>Head and Neck Cancer</condition><condition>Gastric Cancer</condition><condition>Esophageal Cancer</condition><condition>Pancreatic Cancer</condition><condition>ColoRectal Cancer</condition><condition>Pancreatic Neoplasms</condition><condition>Breast Neoplasms</condition><condition>Breast Cancer</condition><condition>Lung Neoplasms</condition><disease>Ovarian Cancer</disease><disease>Lung Cancer</disease><disease>Gastric Cancer</disease><disease>Colorectal Cancer</disease><disease>Esophageal Cancer</disease><disease>Head And Neck Cancer</disease><disease>Pancreatic Cancer</disease><disease>Breast Neoplasms</disease><disease>Pancreatic Neoplasms</disease><disease>Breast Cancer</disease><disease>Lung Neoplasms</disease><disease>Hepatocellular Carcinoma</disease><study_type>Interventional</study_type><full_dataset_link>https://newmdr.ecrin.org/Study/2229591</full_dataset_link><location>United States</location><study_start_month>12</study_start_month><keyword>No Evidence of Disease</keyword><keyword>Post Definitive Surgery</keyword><keyword>High Risk of Relapse</keyword><keyword>Immunotherapy</keyword><keyword>Human Telomerase Reverse Transcriptase (hTERT)</keyword><keyword>Post Adjuvant Therapy</keyword><repository>ECRIN MDR</repository><study_status>Completed</study_status></additional><is_claimable>false</is_claimable><name>hTERT Immunotherapy Alone or in Combination With IL-12 DNA Followed by Electroporation in Adults With Solid Tumors at High Risk of Relapse</name><description>This is a Phase I, open label study to evaluate the safety, tolerability, and immunogenicity of INO-1400 or INO-1401 alone or in combination with INO-9012, delivered by electroporation in subjects with high-risk solid tumor cancer with no evidence of disease after surgery and standard therapy. Subjects will be enrolled into one of ten treatment arms. Subjects will be assessed according to standard of care. Restaging and imaging studies will be performed to assess disease relapse per NCCN guidelines. RECIST will be used to validate the findings in cases of relapse.</description><dates><creation>2014-12-15</creation></dates><accession>2229591</accession><cross_references><ClinicalTrials___gov>NCT02960594</ClinicalTrials___gov></cross_references></HashMap>