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Posted 18 April 2024 PM
Melbourne radiopharmaceutical company Telix has landed a Fast Track designation from the FDA, as it progresses what is likely to be its third commercial product.
The designation was awarded to LX101-CDx, branded Pixclara, for the characterisation of progressive or recurrent glioma using positron emission tomography (PET). There is no FDA-approved targeted PET agent for brain cancer imaging in the US, although it's currently included in both the US and European guidelines for the imaging of gliomas.
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