<HashMap><database>ecrin-mdr-crc</database><scores/><additional><omics_type>Clinical</omics_type><study_start_year>2020</study_start_year><data_sharing_plan>IPD Sharing (as of September 2023): No</data_sharing_plan><condition>Solid Tumor</condition><condition>Colorectal Neoplasms</condition><condition>Advanced Solid Tumor</condition><condition>Ovarian Neoplasms</condition><condition>Lymphoma</condition><condition>Advanced Lymphoma</condition><disease>Solid Tumor</disease><disease>Colorectal Neoplasms</disease><disease>Advanced Solid Tumor</disease><disease>Ovarian Neoplasms</disease><disease>Lymphoma</disease><disease>Advanced Lymphoma</disease><study_type>Interventional</study_type><full_dataset_link>https://newmdr.ecrin.org/Study/2356224</full_dataset_link><location>United States</location><study_start_month>11</study_start_month><keyword>Pembrolizumab</keyword><keyword>Advanced Tumor</keyword><keyword>Microsatellite stable colorectal</keyword><keyword>STING agonist</keyword><keyword>Stimulator of interferon genes</keyword><keyword>B-Cell Lymphomas</keyword><keyword>Microsatellite instable colorectal</keyword><repository>ECRIN MDR</repository><study_status>Active, not recruiting</study_status></additional><is_claimable>false</is_claimable><name>Study of SNX281 in Subjects With Advanced Solid Tumors and Lymphoma</name><description>This clinical trial is evaluating a drug called SNX281 given by itself and in combination with pembrolizumab in participants with advanced solid tumors and lymphoma. The main goals of this study are to:
* Find the recommended dose of SNX281 that can be given to participants safely alone and in combination with pembrolizumab.
* Learn more about the side effects and safety profile of SNX281 alone and in combination with pembrolizumab
* Learn more about pharmacological characteristics of SNX281 alone and in combination with pembrolizumab
* Learn more about effectiveness of SNX281 alone and in combination with pembrolizumab</description><dates><creation>2020-11-15</creation></dates><accession>2356224</accession><cross_references><ClinicalTrials___gov>NCT04609579</ClinicalTrials___gov></cross_references></HashMap>