"2024 represents perhaps our biggest year yet in terms of three new drug approval submissions to the United States (U.S.) Food and Drug Administration (FDA) across our diagnostic portfolio: TLX250-CDx (Zircaix®) for kidney cancer, TLX101-CDx (Pixclara™) for glioblastoma and our “second generation” Prostate-specific membrane antigen (PSMA) imaging product for prostate cancer. Subject to regulatory review and approval, we are already preparing to launch and commercialise these products, following the success of Illuccix®. We have also remained steadfast to our goal of international expansion and the approval of Illuccix® and other products in ex-U.S. markets is anticipated."
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