<HashMap><database>ecrin-mdr-crc</database><scores/><additional><omics_type>Clinical</omics_type><study_start_year>2010</study_start_year><condition>Prostatic Neoplasms</condition><condition>Neoplasm Metastasis</condition><condition>Melanoma</condition><condition>Colorectal Neoplasms</condition><condition>Neoplasms</condition><condition>Head and Neck Neoplasms</condition><disease>Prostatic Neoplasms</disease><disease>Neoplasm Metastasis</disease><disease>Melanoma</disease><disease>Colorectal Neoplasms</disease><disease>Head And Neck Neoplasms</disease><disease>Neoplasms</disease><study_type>Interventional</study_type><full_dataset_link>https://newmdr.ecrin.org/Study/2093934</full_dataset_link><location>United States</location><study_start_month>12</study_start_month><repository>ECRIN MDR</repository><study_status>Completed</study_status></additional><is_claimable>false</is_claimable><name>Exploration of Tumor Accumulation of BAY94-9392 in Patients With Cancer</name><description>The study will be conducted as an open label, single-dose, explorative study with patients with histologically proven cancer and, preferably, tumor positive lesions in previously performed nuclear medicine imaging examinations.
The investigational drug will be given as a single administration in a dose of &lt;/= 0.1 mg BAY94-9392 (300 MBq, +/- 10%). The total duration of the study for each patient will be approximately 8 days.</description><dates><creation>2010-12-15</creation></dates><accession>2093934</accession><cross_references><ClinicalTrials___gov>NCT01186601</ClinicalTrials___gov></cross_references></HashMap>