Telix Pharmaceuticals Doses First Patient in Phase III ProstACT GLOBAL Study of TLX591 for Prostate Cancer
• Telix Pharmaceuticals has dosed the first patient in its Phase III ProstACT GLOBAL study evaluating TLX591, a radioantibody-drug conjugate (rADC) candidate. • The ProstACT GLOBAL study aims to build upon existing data for TLX591, potentially offering benefits when combined with standard-of-care treatments like ARPI or taxanes. • TLX591 represents a potential first-in-class radioantibody-drug conjugate being evaluated in a large, mid-stage patient population for prostate cancer. • The Phase III trial will assess the efficacy and safety of TLX591 in patients with prostate cancer, with the goal of providing a new treatment option.

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Telix's Group Chief Medical Officer, Dr Colin Hayward, highlights the milestone of dosing the first patient in the Prost...