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FDA approves nuclide conjugate drugs for prostate cancer diagnosis!

 Last Update: 2021-12-24
 Source: Internet
 Author: User

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On December 20th, Telix Pharmaceuticals announced that the FDA approved Illuccix (TLX591-CDx) for the marketing of prostate cancer diagnostic imaging

TLX591-CDx is a diagnostic positron emission tomography (PET) tracer targeting prostate specific membrane antigen (PSMA) based on radionuclide-antibody coupling technology (RDC), suitable for metastatic prostate cancer And the diagnosis of recurrent prostate cancer

The National Comprehensive Cancer Network (National Comprehensive Cancer Network) prostate cancer guidelines (2020 edition) recommends TLX591-CDx as a new PET tracer.

In November 2020, Grand Pharmaceuticals signed a cooperation agreement with Telix, and obtained a number of first in class tumor diagnostics (TLX250-CDx, TLX599-CDx) and treatments (TLX591, TLX250, TLX101), including TLX591-CDx, in one fell swoop The exclusive commercialization rights of global innovative RDC products in Greater China (including Hong Kong, Macau, Taiwan), and the company with the largest number of therapeutic + diagnostic RDC drugs in China

Prostate cancer is one of the most common male cancers.

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