Press release from Companies
Publicerat: 2025-08-26 07:05:00
Copenhagen, 26 August 2025 - Curasight A/S ("Curasight" or "the Company" – TICKER: CURAS), a clinical stage radiopharmaceuticals company, today announced the European Medicines Agency (EMA) has approved the company’s clinical trial application (CTA) for the investigation of uTREAT® in a phase 1 trial.
The phase 1 trial is part of Curasight’s theranostic strategy developing more gentle and targeted diagnosis and treatment of certain types of cancer. Dosing the first patient in the trial is expected to occur before the end of the year.
Today’s news means Curasight is now in clinical development with both its diagnostic (uTRACE) and therapeutic (uTREAT) platforms.
“The approval of the CTA underlines the strong progress being made in developing uTREAT as a potential more targeted therapeutic solution for patients with aggressive brain cancer, where there is a strong unmet medical need,” said Curasight’s CEO Ulrich Krasilnikoff and continues, “There has been little progress in treating glioblastoma over the last decades but recently published data from an investigator-initiated Phase II study highlighted the potential of both uTRACE and uTREAT in diagnosing and treating brain cancer where 94% of Grade 4 gliomas -including glioblastomas - were uPAR-positive.”.
For more information regarding Curasight, please contact:
Ulrich Krasilnikoff, CEO
Phone: +45 22 83 01 60
E-mail: uk@curasight.com
Curasight is a clinical development company based in Copenhagen, Denmark. The Company is a pioneer in the field of exploiting a novel Positron Emissions Tomography (PET) imaging (uTRACE®) and Radioligand Therapy (uTREAT®) Theranostic Platform targeting the urokinase-type plasminogen activator receptor ("uPAR"). The technology is expected to improve diagnosis and provide more gentle and efficient treatment of multiple cancer types.