The biodistribution results from Curasight A/S' ("Curasight") testing of uTREAT® for the treatment of glioblastoma are now available. The results are positive and provide "green light" to proceed to the next step. As previously communicated, Curasight's therapeutic technology uTREAT®, a uPAR-targeted radionuclide therapy, entered into preclinical testing in glioblastoma. The first step in testing new targeted radionuclides is the study of biodistribution, where both the binding to the implanted human glioblastoma tumors as well as distribution to organs are tested. The binding to the tumor needs to be sufficiently high to make a therapeutic response likely, and the biodistribution to organs needs to be such that severe side effects are unlikely. uTREAT® has now been tested in a human xenograft glioblastoma tumor model and passed both criteria, which is encouraging and constitutes a "green light" to proceed into further efficacy testing.