<HashMap><database>ecrin-mdr-crc</database><scores/><additional><omics_type>Clinical</omics_type><study_start_year>2021</study_start_year><condition>EGFRI Induced Acneiform Lesions</condition><disease>Egfri Induced Acneiform Lesions</disease><study_type>Interventional</study_type><full_dataset_link>https://newmdr.ecrin.org/Study/2367764</full_dataset_link><location>United States</location><location>Israel</location><study_start_month>4</study_start_month><keyword>EGFRI, Acneiform, Acneiform lesions, Acneiform rash, EGFRI induced skin toxicities</keyword><keyword>LUT014</keyword><repository>ECRIN MDR</repository><study_status>Recruiting</study_status></additional><is_claimable>false</is_claimable><name>LUT014 for the Reduction of Dose-Limiting Acneiform Lesions Associated With EGFRI Treatment of mCRC</name><description>The study evaluates the efficacy and safety of two strengths of LUT014 Gel topically applied once a day for 4 weeks, compared to placebo, in metastatic colorectal cancer (mCRC) patients who developed Grade 2 or non-infected Grade 3 EGFRI induced acneiform lesions</description><dates><creation>2021-04-15</creation></dates><accession>2367764</accession><cross_references><ClinicalTrials___gov>NCT04759664</ClinicalTrials___gov></cross_references></HashMap>