Radiopharmaceutical conjugate of a metabolite and an EPR agent, for targeting tumour cells
US10874753B2 · kind B2 · utility
Assignees
Inventors
Key dates
| Filing date | Sep 25, 2015 |
| Grant date | Dec 29, 2020 |
| Priority date | — |
| Expiry date | Mar 13, 2037 |
Classification
- Technology area (CPC A)Human Necessities
- CPC primaryA61K51/121
- WIPO fieldPharmaceuticals
- WIPO sectorChemistry
Abstract
This invention relates new radiopharmaceutical conjugates for use in improved methods of diagnosis and treatment of cancer. The radiopharmaceutical conjugate comprises, in sequence: a metabolite that targets tumour cells, bound to a chelating agent capable of containing a radionuclide, bound to a linker capable of binding with an EPR agent in vitro or in vivo; or a chelating agent capable of containing a radionuclide, bound to a metabolite that targets tumour cells, bound to a linker capable of binding with an EPR agent in vitro or in vivo. The radiopharmaceutical conjugates of the present invention provide active and passive targeted radio nuclide delivery systems that can help to improve the biodistribution and pharmacological toxicity of the radiopharmaceuticals used for the diagnosis and therapy of cancer.
Source: USPTO / EPO open patent data. Objective bibliographic and citation counts.