1. Academic Validation
  2. Flotufolastat F 18: Diagnostic First Approval

Flotufolastat F 18: Diagnostic First Approval

  • Mol Diagn Ther. 2023 Sep;27(5):631-636. doi: 10.1007/s40291-023-00665-y.
Young-A Heo 1
Affiliations

Affiliation

  • 1 Springer Nature, Private Bag 65901, Mairangi Bay, Auckland, 0754, New Zealand. [email protected].
Abstract

Flotufolastat F 18 (POSLUMA®) is an 18F-labelled radiohybrid (rh) prostate-specific membrane antigen (PSMA)-targeted imaging agent being developed by Blue Earth Diagnostics, a subsidiary of Bracco Imaging, for prostate Cancer imaging. In May 2023, flotufolastat F 18 received its first approval in the USA as a radioactive diagnostic agent for positron emission tomography (PET) of PSMA positive lesions in men with prostate Cancer with suspected metastasis who are candidates for initial definitive therapy or with suspected recurrence based on elevated serum prostate-specific antigen (PSA) level. This article summarizes the milestones in the development of flotufolastat F 18 leading to this first approval.

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