{"id":983448,"date":"2026-07-21T17:08:12","date_gmt":"2026-07-21T21:08:12","guid":{"rendered":"https:\/\/www.marketnewsdesk.com\/index.php\/tlx591-tx-prostact-select-study-published-in-cancers-journal\/"},"modified":"2026-07-21T17:08:12","modified_gmt":"2026-07-21T21:08:12","slug":"tlx591-tx-prostact-select-study-published-in-cancers-journal","status":"publish","type":"post","link":"https:\/\/www.marketnewsdesk.com\/index.php\/tlx591-tx-prostact-select-study-published-in-cancers-journal\/","title":{"rendered":"TLX591-Tx ProstACT SELECT Study Published in Cancers Journal"},"content":{"rendered":"<div class=\"mw_release\">\n<ul>\n<li style=\"text-align:justify\">Peer-reviewed publication of ProstACT SELECT<sup>1<\/sup> results confirm the utility of <sup>68<\/sup>Ga (gallium)-PSMA-PET imaging to select patients for TLX591-Tx therapy using a theranostic approach<sup>2<\/sup>.<\/li>\n<li style=\"text-align:justify\">Consistent with previously reported results<sup>3<\/sup>, the publication highlights TLX591-Tx\u2019s clinical differentiation and safety profile.<\/li>\n<li style=\"text-align:justify\">TLX591-Tx, Telix\u2019s lead PSMA-targeting rADC therapy candidate, is currently being evaluated in ProstACT Global Phase 3 study<sup>4<\/sup> for advanced metastatic prostate cancer.\n<\/li>\n<\/ul>\n<p align=\"justify\">MELBOURNE, Australia and INDIANAPOLIS , July  22, 2026  (GLOBE NEWSWIRE) &#8212; Telix Pharmaceuticals Limited (ASX: TLX, NASDAQ: TLX, \u201cTelix\u201d) today announced publication of results from the ProstACT SELECT study in <em>Cancers<\/em>, a peer-reviewed journal. The Phase 1 study evaluated TLX591-Tx (lutetium-177 (<sup>177<\/sup>Lu) rosopatamab tetraxetan), Telix\u2019s first-in-class prostate-specific membrane antigen (PSMA) targeting radio antibody-drug conjugate (rADC) therapy candidate. The study\u2019s scientific purpose was to evaluate lesion concordance between <sup>68<\/sup>Ga-PSMA-PET<sup>5<\/sup> and multi-time point SPECT<sup>6<\/sup> imaging for patient selection using a \u201ctheranostic\u201d approach.<\/p>\n<p align=\"justify\">The publication highlights TLX591-Tx\u2019s differentiated clinical profile, including an intensified dosing schedule, prolonged tumor retention and low exocrine (salivary) gland irradiation. The authors also concluded that in a heterogeneous population representative of a real-world setting, TLX591-Tx therapy in combination with standard of care (SOC) demonstrated a manageable and predictable safety profile, and indicative efficacy with a median radiographic progression-free survival (rPFS) of 8.8 months reported in evaluable patients.<\/p>\n<p align=\"justify\">Nat Lenzo, MD, Nuclear Medicine Oncologist and Principal Investigator on the ProstACT SELECT study commented, \u201cA key objective of ProstACT SELECT was to determine whether PSMA-PET imaging could reliably identify patients suitable for TLX591-Tx therapy, and the results clearly support this approach. The results provide compelling evidence that the PSMA-PET imaging agent and TLX591-Tx are targeting the same disease sites, supporting the ongoing ProstACT Global trial for mCRPC<sup>7<\/sup>, where there remains significant unmet need for additional treatment options.\u201d<\/p>\n<p align=\"justify\">David N. Cade, MD, Group Chief Medical Officer, Telix, said, \u201cThe publication of ProstACT SELECT data further strengthens the scientific foundation for Telix\u2019s lead therapeutic candidate, TLX591-Tx. The peer-reviewed results support our patient-selection strategy and demonstrate a differentiated pharmacologic profile characterized by durable tumor targeting, hepatobiliary clearance, and a manageable safety profile. Telix is further evaluating TLX591-Tx in the international multi-center Phase 3 ProstACT Global study, where we aim to meaningfully improve outcomes for patients living with advanced prostate cancer.\u201d<\/p>\n<p align=\"justify\">The full paper is available at: <a href=\"https:\/\/www.globenewswire.com\/Tracker?data=AyvVbmNRoXAQ93uEQLOD7tsD6wPWvX8QyU78giDxqOvtnjBt6CWD7np0FFcC54G60T4olzvL3FGRQYGSMnK1nfS4ZVwRdHVf__5al_8uP1uUMC5o5h65H7aY1XkgTU9u\" rel=\"nofollow\" target=\"_blank\">https:\/\/www.mdpi.com\/3989748<\/a><\/p>\n<p align=\"justify\">\n        <strong>About ProstACT SELECT <\/strong>\n      <\/p>\n<p align=\"justify\">The purpose of the ProstACT SELECT trial was to evaluate the utility of <sup>68<\/sup>Ga-PSMA-PET imaging (Illuccix) to select patients for TLX591-Tx rADC therapy. The primary objectives were to determine whole body biodistribution and organ radiation dosimetry and assess the safety and tolerability of TLX591-Tx in patients with advanced mCRPC. rPFS was a secondary study objective.<\/p>\n<p align=\"justify\">\n        <strong>About <\/strong><br \/>\n        <strong>Telix Pharmaceuticals Limited <\/strong>\n      <\/p>\n<p align=\"justify\">Telix Pharmaceuticals (ASX: TLX, NASDAQ: TLX) is a commercial-stage global radiopharmaceutical company, advancing targeted theranostics to improve outcomes for people with cancer across the patient journey. Theranostics pairs a precision diagnostic with a targeted therapy to both diagnose and treat disease.<\/p>\n<p align=\"justify\">Telix&#8217;s commercial franchise is anchored by its prostate cancer imaging portfolio: Illuccix\u00ae (kit for the preparation of gallium-68 gozetotide injection), commercially available in 22 countries including the U.S. and Gozellix\u00ae (kit for the preparation of gallium-68 gozetotide injection), approved by the U.S. Food and Drug Administration (FDA). The Company&#8217;s late-stage therapeutic pipeline includes three assets in pivotal-stage trials: TLX591-Tx (lutetium-177 (<sup>177<\/sup>Lu) rosopatamab tetraxetan) in prostate cancer, TLX101-Tx (<sup>131<\/sup>I-iodofalan) in recurrent glioblastoma, and TLX250-Tx (lutetium (<sup>177<\/sup>Lu) girentuximab tetraxetan) in kidney cancer, additionally complemented by a deep pipeline of next generation assets. TLX591-Tx has not received a marketing authorization in any jurisdiction.<\/p>\n<p align=\"justify\">Telix is headquartered in Melbourne, Australia, with operations across North America, Europe, Latin America and Asia-Pacific. For more information, visit <a href=\"https:\/\/www.globenewswire.com\/Tracker?data=9VR2vaQI5ilyIiJ0zMSuy7CkQTeknszPDHy8qhlwtMfbntYtRhTCVjTVQZnKfnIfR6tr-sPNvhKAASig_islYlr3tlBQQHyOCTGUnAZAc0Y=\" rel=\"nofollow\" target=\"_blank\">www.telixpharma.com<\/a> or follow Telix on <a href=\"https:\/\/www.globenewswire.com\/Tracker?data=nZq0o-9GQp07KaIHM5TXlELg9cN8sZlt5Afj51DVfiVHDCjlDppHEcv_aom6L4v2Yil1srdV6es53-OvKU0c3uh4XOimf8R9gU8sCWklU5ofj_YEMMr3TPVz7BEv1VX6\" rel=\"nofollow\" target=\"_blank\">LinkedIn<\/a>, <a href=\"https:\/\/www.globenewswire.com\/Tracker?data=UnxxpHErG7U94uPj9vQ2DwoPFcb3wD67w63sTWkE3wqDSMbFiV6Q7PSzKIs9h3u52upcKi_IgedQp9N1evu0zA==\" rel=\"nofollow\" target=\"_blank\">X<\/a> and <a href=\"https:\/\/www.globenewswire.com\/Tracker?data=ZPsSduKy1Q8AJn5XYYBS7SYtYaG-uRKBoz11qdyLAVydsCzkXQTLBmBzR1jJxzfpeboJm5nzQQlEk2EHhFe25rMEg-jV19xt1okfNbcV-Hs=\" rel=\"nofollow\" target=\"_blank\">Facebook<\/a>.<\/p>\n<p align=\"justify\">\n        <strong>Telix Contacts<\/strong>\n      <\/p>\n<table style=\"border-collapse: collapse;width:100%;border-collapse:collapse\">\n<tr>\n<td style=\"max-width:40%;width:40%;min-width:40%\">\n            <strong>Investor Relations<\/strong>\n          <\/td>\n<td style=\"max-width:60%;width:60%;min-width:60%\">\n            <strong>Media<\/strong>\n          <\/td>\n<\/tr>\n<tr>\n<td>\n            <strong>Annie Kasparian<\/strong>\n          <\/td>\n<td>\n            <strong>Eliza Schleifstein<\/strong>\n          <\/td>\n<\/tr>\n<tr>\n<td>\n            <a href=\"mailto:Annie.kasparian@telixpharma.com\" rel=\"nofollow\" target=\"_blank\">Annie.kasparian@telixpharma.com<\/a>\n          <\/td>\n<td>\n            <a href=\"mailto:Eliza@schleifsteinpr.com\" rel=\"nofollow\" target=\"_blank\">Eliza@schleifsteinpr.com<\/a>\n          <\/td>\n<\/tr>\n<tr>\n<td>\u00a0<\/td>\n<td>\u00a0<\/td>\n<\/tr>\n<tr>\n<td>\n            <strong>Charlene Jaw<\/strong>\n          <\/td>\n<td>\u00a0<\/td>\n<\/tr>\n<tr>\n<td>\n            <a href=\"mailto:Charlene.jaw@telixpharma.com\" rel=\"nofollow\" target=\"_blank\">Charlene.jaw@telixpharma.com<\/a>\n          <\/td>\n<td>\u00a0<\/td>\n<\/tr>\n<tr>\n<td>\u00a0<\/td>\n<td>\u00a0<\/td>\n<\/tr>\n<\/table>\n<p align=\"center\">Legal Notices<\/p>\n<p align=\"center\">\n        <em>Cautionary Statement Regarding Forward-Looking Statements.\u00a0 <\/em><br \/>\n        \n      <\/p>\n<p align=\"justify\">\n        <em>You should read this announcement together with our risk factors, as disclosed in our most recently filed reports with the Australian Securities Exchange (ASX), U.S. Securities and Exchange Commission (SEC), including our Annual Report on Form 20-F filed with the SEC, or on our website.<\/em>\n      <\/p>\n<p align=\"justify\">\n        <em>The information contained in this announcement is not intended to be an offer for subscription, invitation or recommendation with respect to securities of Telix Pharmaceuticals Limited (Telix) in any jurisdiction, including the United States. The information and opinions contained in this announcement are subject to change without notification. \u202fTo the maximum extent permitted by law, Telix disclaims any obligation or undertaking to update or revise any information or opinions contained in this announcement, including any forward-looking statements (as referred to below), whether as a result of new information, future developments, a change in expectations or assumptions, or otherwise. No representation or warranty, express or implied, is made in relation to the accuracy or completeness of the information contained or opinions expressed in the course of this announcement.<\/em>\n      <\/p>\n<p align=\"justify\">\n        <em>This announcement may contain forward-looking statements, including within the meaning of the U.S. Private Securities Litigation Reform Act of 1995, that relate to anticipated future events, financial performance, plans, strategies or business developments. Forward-looking statements can generally be identified by the use of words such as \u201cmay\u201d, \u201cexpect\u201d, \u201cintend\u201d, \u201cplan\u201d, \u201cestimate\u201d, \u201canticipate\u201d, \u201cbelieve\u201d, \u201coutlook\u201d, \u201cforecast\u201d and \u201cguidance\u201d, or the negative of these words or other similar terms or expressions. Forward-looking statements involve known and unknown risks, uncertainties and other factors that may cause our actual results, levels of activity, performance or achievements to differ materially from any future results, levels of activity, performance or achievements expressed or implied by these forward-looking statements. Forward-looking statements are based on Telix\u2019s good-faith assumptions as to the financial, market, regulatory and other risks and considerations that exist and affect Telix\u2019s business and operations in the future and there can be no assurance that any of the assumptions will prove to be correct. In the context of Telix\u2019s business, forward-looking statements may include, but are not limited to, statements about: the initiation, timing, progress, completion and results of Telix\u2019s preclinical and clinical trials, and Telix\u2019s research and development programs; Telix\u2019s ability to advance product candidates into, enroll and successfully complete, clinical studies, including multi-national clinical trials; the timing or likelihood of regulatory filings and approvals for Telix\u2019s product candidates, manufacturing activities and product marketing activities; Telix\u2019s sales, marketing and distribution and manufacturing capabilities and strategies; the commercialization of Telix\u2019s product candidates, if or when they have been approved; Telix\u2019s ability to obtain an adequate supply of raw materials at reasonable costs for its products and product candidates; estimates of Telix\u2019s expenses, future revenues and capital requirements; Telix\u2019s financial performance; developments relating to Telix\u2019s competitors and industry; the anticipated impact of U.S. and foreign tariffs and other macroeconomic conditions on Telix\u2019s business, including as a result of war or other geopolitical conflicts; and the pricing and reimbursement of Telix\u2019s product candidates, if and after they have been approved. Telix\u2019s actual results, performance or achievements may be materially different from those which may be expressed or implied by such statements, and the differences may be adverse. Accordingly, you should not place undue reliance on these forward-looking statements.<\/em>\n      <\/p>\n<p align=\"justify\">\n        <em>Trademarks and Trade Names. All trademarks and trade names referenced in this press release are the property of Telix Pharmaceuticals Limited (Telix) or, where applicable, the property of their respective owners. For convenience, trademarks and trade names may appear without the \u00ae or \u2122 symbols. Such omissions are not intended to indicate any waiver of rights by Telix or the respective owners. Trademark registration status may vary from country to country. Telix does not intend the use or display of any third-party trademarks or trade names to imply any affiliation with, endorsement by, or sponsorship from those third parties.<\/em>\n      <\/p>\n<p align=\"justify\">\n        <em>\u00a92026 Telix Pharmaceuticals Limited. All rights reserved.<\/em>\n      <\/p>\n<p align=\"justify\">___________________________<\/p>\n<p>\n        <sup>1<\/sup> ClinicalTrials.gov ID: <a href=\"https:\/\/www.globenewswire.com\/Tracker?data=Ld2PjwMPB716JzAQr1lHX0e81C3-gMXhbiUCPM1-nGYVxUX4tS3ZXsivJ1hOInkVhPMm5clmzgqkQNCSEIOZ6Cl1gpmCLRYtI4FsALkOh-wVDkAFIJtbqogLPPzgsRTt\" rel=\"nofollow\" target=\"_blank\">NCT04786847<\/a>.<br \/><sup>2<\/sup> Lenzo et al. <em>Cancers.<\/em> 2026.<br \/><sup>3<\/sup> Telix ASX disclosures October 19, 2023 and May 31, 2024.<br \/><sup>4<\/sup> ClinicalTrials.gov ID:\u00a0<a href=\"https:\/\/www.globenewswire.com\/Tracker?data=KUp08a3MR10kAOjt00NfzhTPRVD7eQe4jFkzzOZmxHxEMtR44k51-MI7t6GNrNjUZK1hRrQ_sexW10eOE_41leUYFwlkAnSABxzOiT2HS7FvcJilHS9E1QnsxjlPGHdy\" rel=\"nofollow\" target=\"_blank\">NCT06520345<\/a>.<br \/><sup>5<\/sup> Imaging of prostate-specific membrane antigen with positron emission tomography.<br \/><sup>6<\/sup> Single-photon emission computed tomography.<br \/><sup>7<\/sup> Metastatic castration-resistant prostate cancer.<\/p>\n<p>      <img decoding=\"async\" alt=\"\" class=\"__GNW8366DE3E__IMG\" src=\"https:\/\/www.globenewswire.com\/newsroom\/ti?nf=OTc2NTQyMiM3NzE1NDgwIzIwODMyNDI=\" \/><br \/>\n      <br \/>\n      <img decoding=\"async\" alt=\"\" src=\"https:\/\/ml.globenewswire.com\/media\/N2Q4ZmNmMmEtMDc5Yi00ZjJhLWE5ZjktOGRmZWJlMDdiMDM1LTEwOTQ4MTMtMjAyNi0wNy0yMS1lbg==\/tiny\/Telix-Pharmaceuticals-Limited.png\" \/>\n    <\/div>\n<div class=\"mw_contactinfo\"><\/div>\n","protected":false},"excerpt":{"rendered":"<p>Peer-reviewed publication of ProstACT SELECT1 results confirm the utility of 68Ga (gallium)-PSMA-PET imaging to select patients for TLX591-Tx therapy using a theranostic approach2. Consistent with previously reported results3, the publication highlights TLX591-Tx\u2019s clinical differentiation and safety profile. TLX591-Tx, Telix\u2019s lead PSMA-targeting rADC therapy candidate, is currently being evaluated in ProstACT Global Phase 3 study4 for advanced metastatic prostate cancer. MELBOURNE, Australia and INDIANAPOLIS , July 22, 2026 (GLOBE NEWSWIRE) &#8212; Telix Pharmaceuticals Limited (ASX: TLX, NASDAQ: TLX, \u201cTelix\u201d) today announced publication of results from the ProstACT SELECT study in Cancers, a peer-reviewed journal. The Phase 1 study evaluated TLX591-Tx (lutetium-177 (177Lu) rosopatamab tetraxetan), Telix\u2019s first-in-class prostate-specific membrane antigen (PSMA) targeting radio antibody-drug conjugate (rADC) therapy candidate. The study\u2019s scientific purpose &hellip; <\/p>\n<p class=\"link-more\"><a href=\"https:\/\/www.marketnewsdesk.com\/index.php\/tlx591-tx-prostact-select-study-published-in-cancers-journal\/\" class=\"more-link\">Continue reading<span class=\"screen-reader-text\"> &#8220;TLX591-Tx ProstACT SELECT Study Published in Cancers Journal&#8221;<\/span><\/a><\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[],"tags":[],"class_list":["post-983448","post","type-post","status-publish","format-standard","hentry"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v28.1 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>TLX591-Tx ProstACT SELECT Study Published in Cancers Journal - Market Newsdesk<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.marketnewsdesk.com\/index.php\/tlx591-tx-prostact-select-study-published-in-cancers-journal\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"TLX591-Tx ProstACT SELECT Study Published in Cancers Journal - Market Newsdesk\" \/>\n<meta property=\"og:description\" content=\"Peer-reviewed publication of ProstACT SELECT1 results confirm the utility of 68Ga (gallium)-PSMA-PET imaging to select patients for TLX591-Tx therapy using a theranostic approach2. Consistent with previously reported results3, the publication highlights TLX591-Tx\u2019s clinical differentiation and safety profile. TLX591-Tx, Telix\u2019s lead PSMA-targeting rADC therapy candidate, is currently being evaluated in ProstACT Global Phase 3 study4 for advanced metastatic prostate cancer. MELBOURNE, Australia and INDIANAPOLIS , July 22, 2026 (GLOBE NEWSWIRE) &#8212; Telix Pharmaceuticals Limited (ASX: TLX, NASDAQ: TLX, \u201cTelix\u201d) today announced publication of results from the ProstACT SELECT study in Cancers, a peer-reviewed journal. The Phase 1 study evaluated TLX591-Tx (lutetium-177 (177Lu) rosopatamab tetraxetan), Telix\u2019s first-in-class prostate-specific membrane antigen (PSMA) targeting radio antibody-drug conjugate (rADC) therapy candidate. The study\u2019s scientific purpose &hellip; Continue reading &quot;TLX591-Tx ProstACT SELECT Study Published in Cancers Journal&quot;\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.marketnewsdesk.com\/index.php\/tlx591-tx-prostact-select-study-published-in-cancers-journal\/\" \/>\n<meta property=\"og:site_name\" content=\"Market Newsdesk\" \/>\n<meta property=\"article:published_time\" content=\"2026-07-21T21:08:12+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/www.globenewswire.com\/newsroom\/ti?nf=OTc2NTQyMiM3NzE1NDgwIzIwODMyNDI=\" \/>\n<meta name=\"author\" content=\"Newsdesk\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Written by\" \/>\n\t<meta name=\"twitter:data1\" content=\"Newsdesk\" \/>\n\t<meta name=\"twitter:label2\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data2\" content=\"7 minutes\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\\\/\\\/schema.org\",\"@graph\":[{\"@type\":\"Article\",\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/tlx591-tx-prostact-select-study-published-in-cancers-journal\\\/#article\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/tlx591-tx-prostact-select-study-published-in-cancers-journal\\\/\"},\"author\":{\"name\":\"Newsdesk\",\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/#\\\/schema\\\/person\\\/482f27a394d4fda80ecb5499e519d979\"},\"headline\":\"TLX591-Tx ProstACT SELECT Study Published in Cancers Journal\",\"datePublished\":\"2026-07-21T21:08:12+00:00\",\"mainEntityOfPage\":{\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/tlx591-tx-prostact-select-study-published-in-cancers-journal\\\/\"},\"wordCount\":1362,\"image\":{\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/tlx591-tx-prostact-select-study-published-in-cancers-journal\\\/#primaryimage\"},\"thumbnailUrl\":\"https:\\\/\\\/www.globenewswire.com\\\/newsroom\\\/ti?nf=OTc2NTQyMiM3NzE1NDgwIzIwODMyNDI=\",\"inLanguage\":\"en-US\"},{\"@type\":\"WebPage\",\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/tlx591-tx-prostact-select-study-published-in-cancers-journal\\\/\",\"url\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/tlx591-tx-prostact-select-study-published-in-cancers-journal\\\/\",\"name\":\"TLX591-Tx ProstACT SELECT Study Published in Cancers Journal - 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Market Newsdesk","robots":{"index":"index","follow":"follow","max-snippet":"max-snippet:-1","max-image-preview":"max-image-preview:large","max-video-preview":"max-video-preview:-1"},"canonical":"https:\/\/www.marketnewsdesk.com\/index.php\/tlx591-tx-prostact-select-study-published-in-cancers-journal\/","og_locale":"en_US","og_type":"article","og_title":"TLX591-Tx ProstACT SELECT Study Published in Cancers Journal - Market Newsdesk","og_description":"Peer-reviewed publication of ProstACT SELECT1 results confirm the utility of 68Ga (gallium)-PSMA-PET imaging to select patients for TLX591-Tx therapy using a theranostic approach2. Consistent with previously reported results3, the publication highlights TLX591-Tx\u2019s clinical differentiation and safety profile. TLX591-Tx, Telix\u2019s lead PSMA-targeting rADC therapy candidate, is currently being evaluated in ProstACT Global Phase 3 study4 for advanced metastatic prostate cancer. MELBOURNE, Australia and INDIANAPOLIS , July 22, 2026 (GLOBE NEWSWIRE) &#8212; Telix Pharmaceuticals Limited (ASX: TLX, NASDAQ: TLX, \u201cTelix\u201d) today announced publication of results from the ProstACT SELECT study in Cancers, a peer-reviewed journal. The Phase 1 study evaluated TLX591-Tx (lutetium-177 (177Lu) rosopatamab tetraxetan), Telix\u2019s first-in-class prostate-specific membrane antigen (PSMA) targeting radio antibody-drug conjugate (rADC) therapy candidate. 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