Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
18F-TATE is a radiolabeled somatostatin analog developed for the diagnostic imaging of neuroendocrine tumors (NETs) using positron emission tomography (PET). It typically comprises the somatostatin receptor-targeting peptide [Tyr3]octreotate (TATE) conjugated to a chelating agent like NOTA, which is then labeled with the radioisotope fluorine-18, often utilizing the aluminum fluoride ([Al18F]2+) complexation method. The tracer specifically targets somatostatin receptors (primarily SSTR2), which are highly expressed on the surface of NET cells. 18F-TATE is designed to overcome the logistical limitations of 68Ga-labeled tracers, such as 68Ga-DOTATATE, by leveraging the longer half-life (110 minutes) and superior imaging characteristics of fluorine-18, enabling centralized production and potentially higher-resolution imaging.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on 18F-TATE.