Radiolabelled octreotate analogues as PET tracers
US10201625B2 · kind B2 · utility
Assignees
Inventors
Key dates
| Filing date | Mar 1, 2012 |
| Grant date | Feb 12, 2019 |
| Priority date | — |
| Expiry date | Mar 1, 2032 |
Classification
- Technology area (CPC C)Chemistry; Metallurgy
- CPC primaryC07B59/008
- WIPO fieldPharmaceuticals
- WIPO sectorChemistry
Abstract
Novel radiotracer(s) for Positron Emission Tomography (PET) imaging are described. Novel radiotracer(s) for Positron Emission Tomography (PET) imaging of neuorendocrine tumors are described. Specifically the present invention describes novel [18F]Fluoroethyltriazol-[Tyr3]Octreotate analogs; in particular those that target somatostatin receptors found on the cell surface of gastroenteropancreatic neuorendocrine tumors. The present invention also describes intermediate(s), precursor(s), pharmaceutical composition(s), methods of making, and methods of use of the novel radiotracer(s).
Source: USPTO / EPO open patent data. Objective bibliographic and citation counts.