This study focuses on patients with intermediate-risk or high-risk prostate cancer who are planned to receive radiotherapy. The research evaluates the effectiveness of using a special imaging technique called PSMA PET (Prostate-Specific Membrane Antigen Positron Emission Tomography) to guide radiation treatment planning. The study uses Locametz, which contains the active substance gozetotide, as an imaging agent that is given through an intravenous injection.
The purpose of the study is to compare the outcomes of radiation treatment when planned using PSMA PET imaging versus standard imaging methods. The study involves two groups of patients – one group will receive radiation therapy planned using conventional imaging, while the other group will have their treatment planned using PSMA PET scans. Each participant will receive a single dose of the imaging agent before their radiation treatment planning.
During the study, patients will be monitored for several years to track their response to treatment and any changes in their cancer status. The monitoring includes regular check-ups and various tests to assess how well the treatment is working. The study medication (Locametz) is already approved for use in medical imaging and will be given as a single dose of up to 259 MBq (a measure of radioactivity).



Germany