MELBOURNE, Australia and INDIANAPOLIS, March 10, 2026 (GLOBE NEWSWIRE) — Telix Pharmaceuticals Limited (ASX: TLX, NASDAQ: TLX, \u201cTelix\u201d) today announces that Part 1 of the ProstACT Global Phase 3 study, the safety and dosimetry lead-in for its therapeutic candidate \u2013 TLX591-Tx (lutetium-177 (177<\/sup>Lu) rosopatamab tetraxetan) \u2013 has achieved its primary objectives, demonstrating an acceptable safety and tolerability profile with no new safety signals observed.<\/p>\n Key findings include:<\/p>\n Part 1 of the study confirmed the safety profile, biodistribution and dosimetry of TLX591-Tx administered in two doses, 14 days apart, in combination with one of three standard of care (SOC) therapies: abiraterone, enzalutamide or docetaxel. The patient population comprised prostate-specific membrane antigen (PSMA) positive metastatic castration resistant prostate cancer (mCRPC) patients previously treated with one androgen receptor pathway inhibitor (ARPI).<\/p>\n ProstACT Global is a differentiated Phase 3 trial comparing PSMA-targeted 177<\/sup>Lu-rADC therapy administered with SOC versus SOC alone, a trial design intended to reflect current global clinical practice1<\/sup>. Telix has already advanced the study into Part 2 \u2013 a 2:1 randomized treatment expansion \u2013 in jurisdictions where the clinical trial has obtained approval from health authorities2<\/sup>. Part 1 data will be presented to the United States (U.S.) Food and Drug Administration (FDA) to seek an Investigational New Drug (IND) amendment to progress Part 2 in the U.S.<\/p>\n Neeraj Agarwal, MD, Professor of Medicine and Presidential Endowed Chair of Cancer Research at Huntsman Cancer Institute, Salt Lake City, and ProstACT Global Principal Investigator and Steering Committee member, commented, \u201cThese results reinforce the feasibility of integrating TLX591-Tx with current standard of care therapies for mCRPC, including ARPIs such as enzalutamide or abiraterone, or docetaxel. Hematologic events align with those typically seen in this patient population and therapeutic class, and these cases resolved quickly. The dosimetry profile, along with the low-grade nature of non-hematologic adverse events, further supports the tolerability profile of this investigational therapy.\u201d<\/p>\n David N. Cade, MD, Group Chief Medical Officer, Telix added, \u201cDespite advances in clinical practice, men with advanced prostate cancer still need improved first and second line treatment options. These results build on prior findings and highlight the potential for TLX591-Tx in combination with contemporary standard of care, to become a new first-line option for patients facing this aggressive disease. We are encouraged by the data and look forward to engaging with the FDA at the earliest opportunity, while continuing to advance enrollment in Part 2 in regions where clinical trial initiation has already been approved.\u201d<\/p>\n Summary results<\/strong><\/p>\n ProstACT Global Part 1 dosed 36 patients, allocated across 3 cohorts:<\/p>\n Safety and tolerability<\/em><\/strong><\/p>\n Dosimetry and biodistribution <\/em><\/strong><\/p>\n About ProstACT Global<\/strong><\/p>\n ProstACT\u00a0Global (ClinicalTrials.gov ID:\u00a0NCT06520345<\/a>) is an international, multicenter trial in two parts: Part 1, safety and dosimetry lead-in with 36 patients (complete); and Part 2, 2:1 randomized global expansion with an overall target enrollment of approximately 490 patients. Eligible patients must have confirmed progressive mCRPC assessed with a\u00a068<\/sup>Ga-PSMA-11 PET4<\/sup>\u00a0imaging agent (such as Illuccix\u00ae, kit for the preparation of gallium-68 (68<\/sup>Ga) gozetotide injection, or Gozellix\u00ae, kit for the preparation of gallium-68 (68<\/sup>Ga) gozetotide injection) following prior treatment with one ARPI.<\/p>\n The antibody approach demonstrates different targeting and pharmacology to that observed in other PSMA-targeted small molecule radioligand therapies (RLT). In contrast to these therapies5<\/sup>, collective long-term follow-up of patients administered with TLX591-Tx has not observed significant acute or delayed kidney toxicity, as the agent is primarily cleared through the liver, a comparatively radioresistant organ, instead of the kidneys6<\/sup>. Due to its large molecular weight, TLX591-Tx also demonstrates minimal salivary and lacrimal gland uptake, reducing dry mouth and dry eyes, common adverse effects of existing PSMA-targeted RLTs7<\/sup>.<\/p>\n Additional information on the Phase 3 ProstACT Global study can be found at:\u00a0https:\/\/telixpharma.com\/prostact\/<\/a><\/p>\n About <\/strong>Telix Pharmaceuticals Limited <\/strong><\/p>\n Telix is a global biopharmaceutical company focused on the development and commercialization of therapeutic and diagnostic radiopharmaceuticals and associated medical technologies, with the goal to address significant unmet medical needs in oncology and rare diseases. With international operations in the United States, United Kingdom, Brazil, Canada, Europe (Belgium and Switzerland), and Japan, Telix is headquartered in Melbourne, Australia. Telix is listed on the Australian Securities Exchange (ASX: TLX) and the Nasdaq Global Select Market (NASDAQ: TLX).<\/p>\n Telix\u2019s Precision Medicine franchise includes llluccix\u00ae, approved in multiple markets globally, and Gozellix\u00ae, approved by the U.S. FDA8<\/sup>. TLX591-Tx has not received a marketing authorization in any jurisdiction.<\/p>\n Visit www.telixpharma.com<\/a> for further information about Telix, including details of the latest share price, ASX and U.S. Securities and Exchange Commission (SEC) filings, investor and analyst presentations, news releases, event details and other publications that may be of interest. You can also follow Telix on LinkedIn<\/a>, X<\/a> and Facebook<\/a>.<\/p>\n\n
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