Tīmeklis2024. gada 7. dec. · Since [18F, natGa]rhPSMA-7 is composed of four stereoisomers ([18F, natGa]rhPSMA-7.1, -7.2, -7.3 and -7.4), we initiated a preclinical selection process to identify the isomer with the most favorable pharmacokinetics for further clinical investigation. A synthetic protocol for enantiopure [19F, natGa]rhPSMA-7 … Tīmeklis2024. gada 1. jūn. · Radiohybrid prostate-specific membrane antigen (rhPSMA) ligands allow for labeling with 18F and radiometals for endoradiotherapy. rhPSMA-7.3 has been designated as a lead compound with promising preclinical data for 177Lu-rhPSMA-7.3, which has shown higher tumor uptake than 177Lu-PSMA I&T. In this retrospective …
Detection rate of 18F-rhPSMA-7.3 PET in patients with suspected ...
Tīmeklis2024. gada 22. nov. · [18F]rhPSMA-7.3 showed a tumor uptake with a tumor-to-background-ratio (TBR) = 2.1–2.5, in 15–60 min. PKM (2TCM) confirmed higher K1 … Tīmeklis2024. gada 22. marts · This phase II trial evaluates Fluorine-18 radiohybrid prostate-specific membrane antigen (18F- rhPSMA)-7.3 positron emission tomography (PET)/computed tomography (CT) scans with and without furosemide for the reduction of bladder activity in patients with prostate cancer that has come back (recurrent) … itil training linkedin learning
Pretherapeutic Comparative Dosimetry of 177Lu-rhPSMA-7.3 and …
Tīmeklis2024. gada 3. dec. · [18F]rhPSMA-7.3 can be used for imaging PSMAexpressing tumours, mainly primary and metastatic prostate cancer, but also non-prostate cancers due to PSMA expression in the neovasculature. As a radiohybrid (therefore the "rh" in the name; not to be confused with recombinant human PSMA) Tīmeklis2024. gada 27. jūl. · Patients receive F-18 rhPSMA-7.3 intravenously (IV) and after approximately 60 minutes of uptake time, will undergo PET/MRI over 60 minutes. Patients with evidence of F-18 rhPSMA-7.3 disease in the first PET/MRI scan undergo a second F-18 rhPSMA-7.3 PET/MRI at 6 months after the second dose of standard … TīmeklisBlue Earth Diagnostics, a Bracco company and recognized leader in the development and commercialization of innovative PET radiopharmaceuticals, announces topline results from its Phase 3 LIGHTHOUSE trial that evaluated the diagnostic performance and safety of 18 F-rhPSMA-7.3 in newly diagnosed prostate cancer. 18 F-rhPSMA … negative impacts of technology articles