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State: 17.08.2024 | 11PM
Mon, 07.10.2024       Telix Pharmaceuticals
AU000000TLX2

MELBOURNE, Australia, Oct. 8, 2024 /PRNewswire/ -- Telix Pharmaceuticals Limited (ASX: TLX, Telix, the Company) today announces that the Australian Therapeutic Goods Administration (TGA) has approved the use of Illuccix® (kit for the preparation of 68Ga-PSMA-11[1] injection) to select patients for PSMA[2]-targeted radionuclide therapy.

Illuccix remains the only PSMA-PET[3] agent approved in Australia, manufactured to GMP[4] standards, and listed on the Medicare Benefits Schedule (MBS) for imaging patients with prostate cancer. This label expansion means that it is now approved to select patients with metastatic prostate cancer for treatment with the only approved PSMA-targeted radionuclide therapy (Lu 177 vipivotide tetraxetan, or Pluvicto®[5]). To qualify for PSMA-targeted therapy, patients should be identified by PSMA imaging[6].

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