<HashMap><database>ecrin-mdr-crc</database><scores/><additional><omics_type>Clinical</omics_type><study_start_year>2013</study_start_year><condition>Prostatic Neoplasms</condition><condition>Metastatic Breast Cancer</condition><condition>Colorectal Cancer</condition><condition>Prostate Cancer</condition><disease>Prostatic Neoplasms</disease><disease>Metastatic Breast Cancer</disease><disease>Colorectal Cancer</disease><disease>Prostate Cancer</disease><study_type>Interventional</study_type><full_dataset_link>https://newmdr.ecrin.org/Study/2157558</full_dataset_link><location>Denmark</location><study_start_month>6</study_start_month><keyword>Wnt-5A</keyword><keyword>Foxy-5</keyword><repository>ECRIN MDR</repository><study_status>Completed</study_status></additional><is_claimable>false</is_claimable><name>Phase I Study to Evaluate Safety, Tolerability, Anti-Tumour Activity and PK Profiles of Foxy-5 in Metastatic Breast, Colon or Prostate Cancer</name><description>The Wnt proteins belong to a family of proteins that have been demonstrated to play a role in the formation and dissemination of tumours. The present project focuses on the critical role of the Wnt-5a protein in the pathobiological processes that lead to metastatic cancer disease.
WntResearch has identified a formylated 6 amino acid peptide fragment, named Foxy-5, which mimick the effects of Wnt-5a to impair migration of epithelial cancer cells and thereby acting anti-metastatic. The aim of the present clinical phase 1 trial is to establish the recommended dose for a clinical phase 2 study and thereby further develop Foxy-5 as a first in class anti-metastatic cancer drug. Foxy-5 is designed to inhibit the development of metastasis by reducing the motility of cancer cells and should thereby increase the survival rates of patients with solid malignant tumours.</description><dates><creation>2013-06-15</creation></dates><accession>2157558</accession><cross_references><ClinicalTrials___gov>NCT02020291</ClinicalTrials___gov></cross_references></HashMap>