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   <title>Form  6-K        Telix Pharmaceuticals     For: Mar 09</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++6-K++++++++Telix+Pharmaceuticals+++++For%3A+Mar+09/26140390.html</link>
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   <title>Form  6-K        Telix Pharmaceuticals     For: Mar 09</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++6-K++++++++Telix+Pharmaceuticals+++++For%3A+Mar+09/26140390.html</link>
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   <title>Form  6-K        Telix Pharmaceuticals     For: Mar 09</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++6-K++++++++Telix+Pharmaceuticals+++++For%3A+Mar+09/26140390.html</link>
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   <title>Telix reports positive Phase 3 Part 1 results for prostate cancer drug</title>
   <link>http://www.streetinsider.com/FDA/Telix+reports+positive+Phase+3+Part+1+results+for+prostate+cancer+drug/26133792.html</link>
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&lt;p&gt;Telix Pharmaceuticals Limited (ASX: TLX, NASDAQ: TLX) announced that Part 1 of its ProstACT Global Phase 3 study for TLX591-Tx achieved primary objectives, demonstrating acceptable safety and tolerability for the prostate cancer treatment.&lt;/p&gt;

&lt;p&gt;The study tested TLX591-Tx, a lutetium-177 radio antibody-drug conjugate therapy, in 36 patients with metastatic castration resistant prostate cancer. Patients received the drug in combination with standard treatments including abiraterone, enzalutamide, or docetaxel.&lt;/p&gt;

&lt;p&gt;Key findings showed no new safety signals, with all patients completing both doses as planned. The most common side effects were fatigue affecting 53% of patients, nausea in 28%, and dry mouth in 25%. Blood-related side</description>
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   <title>Telix reports positive Phase 3 Part 1 results for prostate cancer drug</title>
   <link>http://www.streetinsider.com/FDA/Telix+reports+positive+Phase+3+Part+1+results+for+prostate+cancer+drug/26133792.html</link>
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&lt;p&gt;Telix Pharmaceuticals Limited (ASX: TLX, NASDAQ: TLX) announced that Part 1 of its ProstACT Global Phase 3 study for TLX591-Tx achieved primary objectives, demonstrating acceptable safety and tolerability for the prostate cancer treatment.&lt;/p&gt;

&lt;p&gt;The study tested TLX591-Tx, a lutetium-177 radio antibody-drug conjugate therapy, in 36 patients with metastatic castration resistant prostate cancer. Patients received the drug in combination with standard treatments including abiraterone, enzalutamide, or docetaxel.&lt;/p&gt;

&lt;p&gt;Key findings showed no new safety signals, with all patients completing both doses as planned. The most common side effects were fatigue affecting 53% of patients, nausea in 28%, and dry mouth in 25%. Blood-related side</description>
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   <title>Telix reports positive Phase 3 Part 1 results for prostate cancer drug</title>
   <link>http://www.streetinsider.com/FDA/Telix+reports+positive+Phase+3+Part+1+results+for+prostate+cancer+drug/26133792.html</link>
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&lt;p&gt;Telix Pharmaceuticals Limited (ASX: TLX, NASDAQ: TLX) announced that Part 1 of its ProstACT Global Phase 3 study for TLX591-Tx achieved primary objectives, demonstrating acceptable safety and tolerability for the prostate cancer treatment.&lt;/p&gt;

&lt;p&gt;The study tested TLX591-Tx, a lutetium-177 radio antibody-drug conjugate therapy, in 36 patients with metastatic castration resistant prostate cancer. Patients received the drug in combination with standard treatments including abiraterone, enzalutamide, or docetaxel.&lt;/p&gt;

&lt;p&gt;Key findings showed no new safety signals, with all patients completing both doses as planned. The most common side effects were fatigue affecting 53% of patients, nausea in 28%, and dry mouth in 25%. Blood-related side</description>
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   <title>Telix reports positive Phase 3 Part 1 results for prostate cancer drug</title>
   <link>http://www.streetinsider.com/FDA/Telix+reports+positive+Phase+3+Part+1+results+for+prostate+cancer+drug/26133792.html</link>
   <description>

&lt;p&gt;Telix Pharmaceuticals Limited (ASX: TLX, NASDAQ: TLX) announced that Part 1 of its ProstACT Global Phase 3 study for TLX591-Tx achieved primary objectives, demonstrating acceptable safety and tolerability for the prostate cancer treatment.&lt;/p&gt;

&lt;p&gt;The study tested TLX591-Tx, a lutetium-177 radio antibody-drug conjugate therapy, in 36 patients with metastatic castration resistant prostate cancer. Patients received the drug in combination with standard treatments including abiraterone, enzalutamide, or docetaxel.&lt;/p&gt;

&lt;p&gt;Key findings showed no new safety signals, with all patients completing both doses as planned. The most common side effects were fatigue affecting 53% of patients, nausea in 28%, and dry mouth in 25%. Blood-related side</description>
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   <title>Telix reports positive Phase 3 Part 1 results for prostate cancer drug</title>
   <link>http://www.streetinsider.com/FDA/Telix+reports+positive+Phase+3+Part+1+results+for+prostate+cancer+drug/26133792.html</link>
   <description>

&lt;p&gt;Telix Pharmaceuticals Limited (ASX: TLX, NASDAQ: TLX) announced that Part 1 of its ProstACT Global Phase 3 study for TLX591-Tx achieved primary objectives, demonstrating acceptable safety and tolerability for the prostate cancer treatment.&lt;/p&gt;

&lt;p&gt;The study tested TLX591-Tx, a lutetium-177 radio antibody-drug conjugate therapy, in 36 patients with metastatic castration resistant prostate cancer. Patients received the drug in combination with standard treatments including abiraterone, enzalutamide, or docetaxel.&lt;/p&gt;

&lt;p&gt;Key findings showed no new safety signals, with all patients completing both doses as planned. The most common side effects were fatigue affecting 53% of patients, nausea in 28%, and dry mouth in 25%. Blood-related side</description>
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   <title>Telix reports positive Phase 3 Part 1 results for prostate cancer drug</title>
   <link>http://www.streetinsider.com/FDA/Telix+reports+positive+Phase+3+Part+1+results+for+prostate+cancer+drug/26133792.html</link>
   <description>

&lt;p&gt;Telix Pharmaceuticals Limited (ASX: TLX, NASDAQ: TLX) announced that Part 1 of its ProstACT Global Phase 3 study for TLX591-Tx achieved primary objectives, demonstrating acceptable safety and tolerability for the prostate cancer treatment.&lt;/p&gt;

&lt;p&gt;The study tested TLX591-Tx, a lutetium-177 radio antibody-drug conjugate therapy, in 36 patients with metastatic castration resistant prostate cancer. Patients received the drug in combination with standard treatments including abiraterone, enzalutamide, or docetaxel.&lt;/p&gt;

&lt;p&gt;Key findings showed no new safety signals, with all patients completing both doses as planned. The most common side effects were fatigue affecting 53% of patients, nausea in 28%, and dry mouth in 25%. Blood-related side</description>
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   <title>Telix reports positive Phase 3 Part 1 results for prostate cancer drug</title>
   <link>http://www.streetinsider.com/FDA/Telix+reports+positive+Phase+3+Part+1+results+for+prostate+cancer+drug/26133792.html</link>
   <description>

&lt;p&gt;Telix Pharmaceuticals Limited (ASX: TLX, NASDAQ: TLX) announced that Part 1 of its ProstACT Global Phase 3 study for TLX591-Tx achieved primary objectives, demonstrating acceptable safety and tolerability for the prostate cancer treatment.&lt;/p&gt;

&lt;p&gt;The study tested TLX591-Tx, a lutetium-177 radio antibody-drug conjugate therapy, in 36 patients with metastatic castration resistant prostate cancer. Patients received the drug in combination with standard treatments including abiraterone, enzalutamide, or docetaxel.&lt;/p&gt;

&lt;p&gt;Key findings showed no new safety signals, with all patients completing both doses as planned. The most common side effects were fatigue affecting 53% of patients, nausea in 28%, and dry mouth in 25%. Blood-related side</description>
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   <title>Telix reports positive Phase 3 Part 1 results for prostate cancer drug</title>
   <link>http://www.streetinsider.com/FDA/Telix+reports+positive+Phase+3+Part+1+results+for+prostate+cancer+drug/26133792.html</link>
   <description>

&lt;p&gt;Telix Pharmaceuticals Limited (ASX: TLX, NASDAQ: TLX) announced that Part 1 of its ProstACT Global Phase 3 study for TLX591-Tx achieved primary objectives, demonstrating acceptable safety and tolerability for the prostate cancer treatment.&lt;/p&gt;

&lt;p&gt;The study tested TLX591-Tx, a lutetium-177 radio antibody-drug conjugate therapy, in 36 patients with metastatic castration resistant prostate cancer. Patients received the drug in combination with standard treatments including abiraterone, enzalutamide, or docetaxel.&lt;/p&gt;

&lt;p&gt;Key findings showed no new safety signals, with all patients completing both doses as planned. The most common side effects were fatigue affecting 53% of patients, nausea in 28%, and dry mouth in 25%. Blood-related side</description>
   <guid isPermaLink="true">http://www.streetinsider.com/FDA/Telix+reports+positive+Phase+3+Part+1+results+for+prostate+cancer+drug/26133792.html</guid>
   <pubDate>Mon, 09 Mar 2026 19:20:14 -0400</pubDate>
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   <title>ProstACT Global Phase 3 Study (Part 1) Achieves Primary Objectives</title>
   <link>http://www.streetinsider.com/Press+Releases/ProstACT+Global+Phase+3+Study+%28Part+1%29+Achieves+Primary+Objectives/26133787.html</link>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;Webcast and conference call to be held today, Tuesday March 10 at 9:30 a.m. AEDT (Monday March 9 at 6:30 p.m. EDT). Investors can register at the following link: &lt;a target=&quot;_blank&quot; href=&quot;https://s1.c-conf.com/diamondpass/10053620-ju7y6t.html&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;https://s1.c-conf.com/diamondpass/10053620-ju7y6t.html&lt;/a&gt;&lt;br/&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p align=&quot;justify&quot;&gt;MELBOURNE, Australia and INDIANAPOLIS, March  10, 2026  (GLOBE NEWSWIRE) --  Telix Pharmaceuticals Limited (ASX: TLX, NASDAQ: TLX, “Telix”) today announces that Part 1 of the ProstACT Global Phase 3 study, the safety and dosimetry lead-in for its therapeutic candidate – TLX591-Tx (lutetium-177 (177Lu) rosopatamab tetraxetan) – has achieved its primary objectives, demonstrating an acceptable safety and tolerability profile with</description>
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   <pubDate>Mon, 09 Mar 2026 19:19:00 -0400</pubDate>
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   <title>ProstACT Global Phase 3 Study (Part 1) Achieves Primary Objectives</title>
   <link>http://www.streetinsider.com/Press+Releases/ProstACT+Global+Phase+3+Study+%28Part+1%29+Achieves+Primary+Objectives/26133787.html</link>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;Webcast and conference call to be held today, Tuesday March 10 at 9:30 a.m. AEDT (Monday March 9 at 6:30 p.m. EDT). Investors can register at the following link: &lt;a target=&quot;_blank&quot; href=&quot;https://s1.c-conf.com/diamondpass/10053620-ju7y6t.html&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;https://s1.c-conf.com/diamondpass/10053620-ju7y6t.html&lt;/a&gt;&lt;br/&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p align=&quot;justify&quot;&gt;MELBOURNE, Australia and INDIANAPOLIS, March  10, 2026  (GLOBE NEWSWIRE) --  Telix Pharmaceuticals Limited (ASX: TLX, NASDAQ: TLX, “Telix”) today announces that Part 1 of the ProstACT Global Phase 3 study, the safety and dosimetry lead-in for its therapeutic candidate – TLX591-Tx (lutetium-177 (177Lu) rosopatamab tetraxetan) – has achieved its primary objectives, demonstrating an acceptable safety and tolerability profile with</description>
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   <title>ProstACT Global Phase 3 Study (Part 1) Achieves Primary Objectives</title>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;Webcast and conference call to be held today, Tuesday March 10 at 9:30 a.m. AEDT (Monday March 9 at 6:30 p.m. EDT). Investors can register at the following link: &lt;a target=&quot;_blank&quot; href=&quot;https://s1.c-conf.com/diamondpass/10053620-ju7y6t.html&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;https://s1.c-conf.com/diamondpass/10053620-ju7y6t.html&lt;/a&gt;&lt;br/&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p align=&quot;justify&quot;&gt;MELBOURNE, Australia and INDIANAPOLIS, March  10, 2026  (GLOBE NEWSWIRE) --  Telix Pharmaceuticals Limited (ASX: TLX, NASDAQ: TLX, “Telix”) today announces that Part 1 of the ProstACT Global Phase 3 study, the safety and dosimetry lead-in for its therapeutic candidate – TLX591-Tx (lutetium-177 (177Lu) rosopatamab tetraxetan) – has achieved its primary objectives, demonstrating an acceptable safety and tolerability profile with</description>
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   <title>ProstACT Global Phase 3 Study (Part 1) Achieves Primary Objectives</title>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;Webcast and conference call to be held today, Tuesday March 10 at 9:30 a.m. AEDT (Monday March 9 at 6:30 p.m. EDT). Investors can register at the following link: &lt;a target=&quot;_blank&quot; href=&quot;https://s1.c-conf.com/diamondpass/10053620-ju7y6t.html&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;https://s1.c-conf.com/diamondpass/10053620-ju7y6t.html&lt;/a&gt;&lt;br/&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p align=&quot;justify&quot;&gt;MELBOURNE, Australia and INDIANAPOLIS, March  10, 2026  (GLOBE NEWSWIRE) --  Telix Pharmaceuticals Limited (ASX: TLX, NASDAQ: TLX, “Telix”) today announces that Part 1 of the ProstACT Global Phase 3 study, the safety and dosimetry lead-in for its therapeutic candidate – TLX591-Tx (lutetium-177 (177Lu) rosopatamab tetraxetan) – has achieved its primary objectives, demonstrating an acceptable safety and tolerability profile with</description>
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   <title>ProstACT Global Phase 3 Study (Part 1) Achieves Primary Objectives</title>
   <link>http://www.streetinsider.com/Press+Releases/ProstACT+Global+Phase+3+Study+%28Part+1%29+Achieves+Primary+Objectives/26133787.html</link>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;Webcast and conference call to be held today, Tuesday March 10 at 9:30 a.m. AEDT (Monday March 9 at 6:30 p.m. EDT). Investors can register at the following link: &lt;a target=&quot;_blank&quot; href=&quot;https://s1.c-conf.com/diamondpass/10053620-ju7y6t.html&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;https://s1.c-conf.com/diamondpass/10053620-ju7y6t.html&lt;/a&gt;&lt;br/&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p align=&quot;justify&quot;&gt;MELBOURNE, Australia and INDIANAPOLIS, March  10, 2026  (GLOBE NEWSWIRE) --  Telix Pharmaceuticals Limited (ASX: TLX, NASDAQ: TLX, “Telix”) today announces that Part 1 of the ProstACT Global Phase 3 study, the safety and dosimetry lead-in for its therapeutic candidate – TLX591-Tx (lutetium-177 (177Lu) rosopatamab tetraxetan) – has achieved its primary objectives, demonstrating an acceptable safety and tolerability profile with</description>
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   <title>ProstACT Global Phase 3 Study (Part 1) Achieves Primary Objectives</title>
   <link>http://www.streetinsider.com/Press+Releases/ProstACT+Global+Phase+3+Study+%28Part+1%29+Achieves+Primary+Objectives/26133787.html</link>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;Webcast and conference call to be held today, Tuesday March 10 at 9:30 a.m. AEDT (Monday March 9 at 6:30 p.m. EDT). Investors can register at the following link: &lt;a target=&quot;_blank&quot; href=&quot;https://s1.c-conf.com/diamondpass/10053620-ju7y6t.html&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;https://s1.c-conf.com/diamondpass/10053620-ju7y6t.html&lt;/a&gt;&lt;br/&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p align=&quot;justify&quot;&gt;MELBOURNE, Australia and INDIANAPOLIS, March  10, 2026  (GLOBE NEWSWIRE) --  Telix Pharmaceuticals Limited (ASX: TLX, NASDAQ: TLX, “Telix”) today announces that Part 1 of the ProstACT Global Phase 3 study, the safety and dosimetry lead-in for its therapeutic candidate – TLX591-Tx (lutetium-177 (177Lu) rosopatamab tetraxetan) – has achieved its primary objectives, demonstrating an acceptable safety and tolerability profile with</description>
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   <title>ProstACT Global Phase 3 Study (Part 1) Achieves Primary Objectives</title>
   <link>http://www.streetinsider.com/Press+Releases/ProstACT+Global+Phase+3+Study+%28Part+1%29+Achieves+Primary+Objectives/26133787.html</link>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;Webcast and conference call to be held today, Tuesday March 10 at 9:30 a.m. AEDT (Monday March 9 at 6:30 p.m. EDT). Investors can register at the following link: &lt;a target=&quot;_blank&quot; href=&quot;https://s1.c-conf.com/diamondpass/10053620-ju7y6t.html&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;https://s1.c-conf.com/diamondpass/10053620-ju7y6t.html&lt;/a&gt;&lt;br/&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p align=&quot;justify&quot;&gt;MELBOURNE, Australia and INDIANAPOLIS, March  10, 2026  (GLOBE NEWSWIRE) --  Telix Pharmaceuticals Limited (ASX: TLX, NASDAQ: TLX, “Telix”) today announces that Part 1 of the ProstACT Global Phase 3 study, the safety and dosimetry lead-in for its therapeutic candidate – TLX591-Tx (lutetium-177 (177Lu) rosopatamab tetraxetan) – has achieved its primary objectives, demonstrating an acceptable safety and tolerability profile with</description>
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   <title>ProstACT Global Phase 3 Study (Part 1) Achieves Primary Objectives</title>
   <link>http://www.streetinsider.com/Press+Releases/ProstACT+Global+Phase+3+Study+%28Part+1%29+Achieves+Primary+Objectives/26133787.html</link>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;Webcast and conference call to be held today, Tuesday March 10 at 9:30 a.m. AEDT (Monday March 9 at 6:30 p.m. EDT). Investors can register at the following link: &lt;a target=&quot;_blank&quot; href=&quot;https://s1.c-conf.com/diamondpass/10053620-ju7y6t.html&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;https://s1.c-conf.com/diamondpass/10053620-ju7y6t.html&lt;/a&gt;&lt;br/&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p align=&quot;justify&quot;&gt;MELBOURNE, Australia and INDIANAPOLIS, March  10, 2026  (GLOBE NEWSWIRE) --  Telix Pharmaceuticals Limited (ASX: TLX, NASDAQ: TLX, “Telix”) today announces that Part 1 of the ProstACT Global Phase 3 study, the safety and dosimetry lead-in for its therapeutic candidate – TLX591-Tx (lutetium-177 (177Lu) rosopatamab tetraxetan) – has achieved its primary objectives, demonstrating an acceptable safety and tolerability profile with</description>
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   <title>ProstACT Global Phase 3 Study (Part 1) Achieves Primary Objectives</title>
   <link>http://www.streetinsider.com/Press+Releases/ProstACT+Global+Phase+3+Study+%28Part+1%29+Achieves+Primary+Objectives/26133787.html</link>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;Webcast and conference call to be held today, Tuesday March 10 at 9:30 a.m. AEDT (Monday March 9 at 6:30 p.m. EDT). Investors can register at the following link: &lt;a target=&quot;_blank&quot; href=&quot;https://s1.c-conf.com/diamondpass/10053620-ju7y6t.html&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;https://s1.c-conf.com/diamondpass/10053620-ju7y6t.html&lt;/a&gt;&lt;br/&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p align=&quot;justify&quot;&gt;MELBOURNE, Australia and INDIANAPOLIS, March  10, 2026  (GLOBE NEWSWIRE) --  Telix Pharmaceuticals Limited (ASX: TLX, NASDAQ: TLX, “Telix”) today announces that Part 1 of the ProstACT Global Phase 3 study, the safety and dosimetry lead-in for its therapeutic candidate – TLX591-Tx (lutetium-177 (177Lu) rosopatamab tetraxetan) – has achieved its primary objectives, demonstrating an acceptable safety and tolerability profile with</description>
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   <title>ProstACT Global Phase 3 Study (Part 1) Achieves Primary Objectives</title>
   <link>http://www.streetinsider.com/Globe+Newswire/ProstACT+Global+Phase+3+Study+%28Part+1%29+Achieves+Primary+Objectives/26133787.html</link>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;Webcast and conference call to be held today, Tuesday March 10 at 9:30 a.m. AEDT (Monday March 9 at 6:30 p.m. EDT). Investors can register at the following link: &lt;a target=&quot;_blank&quot; href=&quot;https://s1.c-conf.com/diamondpass/10053620-ju7y6t.html&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;https://s1.c-conf.com/diamondpass/10053620-ju7y6t.html&lt;/a&gt;&lt;br/&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p align=&quot;justify&quot;&gt;MELBOURNE, Australia and INDIANAPOLIS, March  10, 2026  (GLOBE NEWSWIRE) --  Telix Pharmaceuticals Limited (ASX: TLX, NASDAQ: TLX, “Telix”) today announces that Part 1 of the ProstACT Global Phase 3 study, the safety and dosimetry lead-in for its therapeutic candidate – TLX591-Tx (lutetium-177 (177Lu) rosopatamab tetraxetan) – has achieved its primary objectives, demonstrating an acceptable safety and tolerability profile with</description>
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   <title>ProstACT Global Phase 3 Study (Part 1) Achieves Primary Objectives</title>
   <link>http://www.streetinsider.com/Globe+Newswire/ProstACT+Global+Phase+3+Study+%28Part+1%29+Achieves+Primary+Objectives/26133787.html</link>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;Webcast and conference call to be held today, Tuesday March 10 at 9:30 a.m. AEDT (Monday March 9 at 6:30 p.m. EDT). Investors can register at the following link: &lt;a target=&quot;_blank&quot; href=&quot;https://s1.c-conf.com/diamondpass/10053620-ju7y6t.html&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;https://s1.c-conf.com/diamondpass/10053620-ju7y6t.html&lt;/a&gt;&lt;br/&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p align=&quot;justify&quot;&gt;MELBOURNE, Australia and INDIANAPOLIS, March  10, 2026  (GLOBE NEWSWIRE) --  Telix Pharmaceuticals Limited (ASX: TLX, NASDAQ: TLX, “Telix”) today announces that Part 1 of the ProstACT Global Phase 3 study, the safety and dosimetry lead-in for its therapeutic candidate – TLX591-Tx (lutetium-177 (177Lu) rosopatamab tetraxetan) – has achieved its primary objectives, demonstrating an acceptable safety and tolerability profile with</description>
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   <title>ProstACT Global Phase 3 Study (Part 1) Achieves Primary Objectives</title>
   <link>http://www.streetinsider.com/Globe+Newswire/ProstACT+Global+Phase+3+Study+%28Part+1%29+Achieves+Primary+Objectives/26133787.html</link>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;Webcast and conference call to be held today, Tuesday March 10 at 9:30 a.m. AEDT (Monday March 9 at 6:30 p.m. EDT). Investors can register at the following link: &lt;a target=&quot;_blank&quot; href=&quot;https://s1.c-conf.com/diamondpass/10053620-ju7y6t.html&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;https://s1.c-conf.com/diamondpass/10053620-ju7y6t.html&lt;/a&gt;&lt;br/&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p align=&quot;justify&quot;&gt;MELBOURNE, Australia and INDIANAPOLIS, March  10, 2026  (GLOBE NEWSWIRE) --  Telix Pharmaceuticals Limited (ASX: TLX, NASDAQ: TLX, “Telix”) today announces that Part 1 of the ProstACT Global Phase 3 study, the safety and dosimetry lead-in for its therapeutic candidate – TLX591-Tx (lutetium-177 (177Lu) rosopatamab tetraxetan) – has achieved its primary objectives, demonstrating an acceptable safety and tolerability profile with</description>
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   <title>ProstACT Global Phase 3 Study (Part 1) Achieves Primary Objectives</title>
   <link>http://www.streetinsider.com/Globe+Newswire/ProstACT+Global+Phase+3+Study+%28Part+1%29+Achieves+Primary+Objectives/26133787.html</link>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;Webcast and conference call to be held today, Tuesday March 10 at 9:30 a.m. AEDT (Monday March 9 at 6:30 p.m. EDT). Investors can register at the following link: &lt;a target=&quot;_blank&quot; href=&quot;https://s1.c-conf.com/diamondpass/10053620-ju7y6t.html&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;https://s1.c-conf.com/diamondpass/10053620-ju7y6t.html&lt;/a&gt;&lt;br/&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p align=&quot;justify&quot;&gt;MELBOURNE, Australia and INDIANAPOLIS, March  10, 2026  (GLOBE NEWSWIRE) --  Telix Pharmaceuticals Limited (ASX: TLX, NASDAQ: TLX, “Telix”) today announces that Part 1 of the ProstACT Global Phase 3 study, the safety and dosimetry lead-in for its therapeutic candidate – TLX591-Tx (lutetium-177 (177Lu) rosopatamab tetraxetan) – has achieved its primary objectives, demonstrating an acceptable safety and tolerability profile with</description>
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   <pubDate>Mon, 09 Mar 2026 19:19:00 -0400</pubDate>
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  <item>
   <title>ProstACT Global Phase 3 Study (Part 1) Achieves Primary Objectives</title>
   <link>http://www.streetinsider.com/Globe+Newswire/ProstACT+Global+Phase+3+Study+%28Part+1%29+Achieves+Primary+Objectives/26133787.html</link>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;Webcast and conference call to be held today, Tuesday March 10 at 9:30 a.m. AEDT (Monday March 9 at 6:30 p.m. EDT). Investors can register at the following link: &lt;a target=&quot;_blank&quot; href=&quot;https://s1.c-conf.com/diamondpass/10053620-ju7y6t.html&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;https://s1.c-conf.com/diamondpass/10053620-ju7y6t.html&lt;/a&gt;&lt;br/&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p align=&quot;justify&quot;&gt;MELBOURNE, Australia and INDIANAPOLIS, March  10, 2026  (GLOBE NEWSWIRE) --  Telix Pharmaceuticals Limited (ASX: TLX, NASDAQ: TLX, “Telix”) today announces that Part 1 of the ProstACT Global Phase 3 study, the safety and dosimetry lead-in for its therapeutic candidate – TLX591-Tx (lutetium-177 (177Lu) rosopatamab tetraxetan) – has achieved its primary objectives, demonstrating an acceptable safety and tolerability profile with</description>
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