Press release from Companies
Published: 2014-11-10 09:26:37
WntResearch AB announces that the Phase 1 trial has reached dose levels equivalent to the effective dose level in pre-clinical models with no dose limiting toxicity observed. Therefore, the company has decided to limit the enrollment of patients to those patients with highest likelihood to respond to Foxy-5. This means that we will limit the enrollment to prostate-, colon- and breast cancer patients with no or low level of Wnt-5a expression at our two sites at the Herlev University Hospital and the Rigshospitalet, Phase 1 Unit in Copenhagen. Consequently, the completion of the study is expected to be postponed from Q4 2014 to Q1 2015.