<HashMap><database>ecrin-mdr-crc</database><scores/><additional><omics_type>Clinical</omics_type><study_start_year>2015</study_start_year><condition>Neoplasm Metastasis</condition><condition>Melanoma</condition><condition>Solid Tumors</condition><disease>Neoplasm Metastasis</disease><disease>Melanoma</disease><disease>Solid Tumors</disease><study_type>Interventional</study_type><full_dataset_link>https://newmdr.ecrin.org/Study/2179977</full_dataset_link><location>United States</location><location>Australia</location><study_start_month>1</study_start_month><keyword>Metastatic Solid Tumors</keyword><keyword>Maximum Tolerated Dose</keyword><keyword>Relapsed or refractory, BRAFV600 or RAS-mutated solid tumors</keyword><keyword>Thyroid carcinomas</keyword><keyword>Locally Advanced Tumors</keyword><keyword>Non -small cell lung cancer [NSCLC]</keyword><keyword>Pancreatic ductal Adenocarcinomas</keyword><keyword>Colorectal Carcinomas Papillary</keyword><repository>ECRIN MDR</repository><study_status>Terminated</study_status></additional><is_claimable>false</is_claimable><name>Safety and PK Study of CC-90003 in Relapsed/Refractory Solid Tumors</name><description>The CC-90003-ST -001 trial is a first-in-man, open-label study in subjects with locally-advanced or wide spread cancers to determine if CC-90003 (an oral medication) can be adequately tolerated with minimal side effects.</description><dates><creation>2015-01-15</creation></dates><accession>2179977</accession><cross_references><ClinicalTrials___gov>NCT02313012</ClinicalTrials___gov></cross_references></HashMap>