<HashMap><database>ecrin-mdr-crc</database><scores/><additional><omics_type>Clinical</omics_type><study_start_year>2019</study_start_year><data_sharing_plan>IPD Sharing (as of February 2022): No</data_sharing_plan><condition>Ovarian Cancer</condition><condition>Leukemia, Myeloid</condition><condition>Triple Negative Breast Neoplasms</condition><condition>Colorectal Cancer</condition><condition>Small Cell Lung Carcinoma</condition><condition>Triple-negative Breast Cancer</condition><condition>Small-cell Lung Cancer</condition><condition>Leukemia, Myeloid, Acute</condition><condition>Acute Myelogenous Leukemia</condition><disease>Ovarian Cancer</disease><disease>Leukemia, Myeloid</disease><disease>Triple Negative Breast Neoplasms</disease><disease>Colorectal Cancer</disease><disease>Small Cell Lung Carcinoma</disease><disease>Triple-negative Breast Cancer</disease><disease>Small-cell Lung Cancer</disease><disease>Leukemia, Myeloid, Acute</disease><disease>Acute Myelogenous Leukemia</disease><study_type>Interventional</study_type><full_dataset_link>https://newmdr.ecrin.org/Study/2291112</full_dataset_link><location>United States</location><study_start_month>6</study_start_month><keyword>Checkpoint inhibitor</keyword><keyword>SLS-001</keyword><keyword>Combination immunotherapy</keyword><keyword>Off-the-shelf vaccine</keyword><keyword>Peptide vaccine</keyword><keyword>Immuno-oncology</keyword><keyword>WT1-expressing tumors</keyword><keyword>Pembrolizumab</keyword><keyword>PD1 inhibitor</keyword><keyword>Galinpepimut-S</keyword><keyword>Multivalent</keyword><keyword>HLA allele</keyword><keyword>Heteroclitic</keyword><keyword>WT1 analog peptide vaccine</keyword><keyword>WT1 vaccine</keyword><repository>ECRIN MDR</repository><study_status>Active, not recruiting</study_status></additional><is_claimable>false</is_claimable><name>Galinpepimut-S in Combination With Pembrolizumab in Patients With Selected Advanced Cancers</name><description>To evaluate the safety and tolerability of galinpepimut-S in combination with pembrolizumab in patients with selected advanced cancers. Patients will be followed long-term for Overall Survival (OS) and safety. The study will enroll approximately 90 patients and maximum study treatment duration is approximately 2.13 years.</description><dates><creation>2019-06-15</creation></dates><accession>2291112</accession><cross_references><ClinicalTrials___gov>NCT03761914</ClinicalTrials___gov></cross_references></HashMap>