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   <title>Beacon Therapeutics Announces Positive Phase 2 Interim 6-Month Data from DAWN Trial of Laru-zova in Patients with X-linked Retinitis Pigmentosa (XLRP) at ARVO 2025</title>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;Data showed improvements across several key measures of visual function, including low luminance visual acuity and microperimetry&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Laru-zova was generally well-tolerated by DAWN participants at 6 months&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;LONDON and CAMBRIDGE, Mass., May  06, 2025  (GLOBE NEWSWIRE) -- Beacon Therapeutics Holdings Limited (‘Beacon Therapeutics’ or ‘the Company’), a leading clinical-stage biotechnology company with a mission to save and restore the vision of patients with blinding retinal diseases, today announced 6-month interim safety and efficacy results from the Phase 2 DAWN trial of the Company’s lead program, laru-zova (laruparetigene zovaparvovec), in patients with X-linked retinitis</description>
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   <title>Beacon Therapeutics Announces Positive Phase 2 Interim 6-Month Data from DAWN Trial of Laru-zova in Patients with X-linked Retinitis Pigmentosa (XLRP) at ARVO 2025</title>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;Data showed improvements across several key measures of visual function, including low luminance visual acuity and microperimetry&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Laru-zova was generally well-tolerated by DAWN participants at 6 months&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;LONDON and CAMBRIDGE, Mass., May  06, 2025  (GLOBE NEWSWIRE) -- Beacon Therapeutics Holdings Limited (‘Beacon Therapeutics’ or ‘the Company’), a leading clinical-stage biotechnology company with a mission to save and restore the vision of patients with blinding retinal diseases, today announced 6-month interim safety and efficacy results from the Phase 2 DAWN trial of the Company’s lead program, laru-zova (laruparetigene zovaparvovec), in patients with X-linked retinitis</description>
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   <title>Beacon Therapeutics Announces Positive Phase 2 Interim 6-Month Data from DAWN Trial of Laru-zova in Patients with X-linked Retinitis Pigmentosa (XLRP) at ARVO 2025</title>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;Data showed improvements across several key measures of visual function, including low luminance visual acuity and microperimetry&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Laru-zova was generally well-tolerated by DAWN participants at 6 months&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;LONDON and CAMBRIDGE, Mass., May  06, 2025  (GLOBE NEWSWIRE) -- Beacon Therapeutics Holdings Limited (‘Beacon Therapeutics’ or ‘the Company’), a leading clinical-stage biotechnology company with a mission to save and restore the vision of patients with blinding retinal diseases, today announced 6-month interim safety and efficacy results from the Phase 2 DAWN trial of the Company’s lead program, laru-zova (laruparetigene zovaparvovec), in patients with X-linked retinitis</description>
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   <title>Beacon Therapeutics Announces Positive Phase 2 Interim 6-Month Data from DAWN Trial of Laru-zova in Patients with X-linked Retinitis Pigmentosa (XLRP) at ARVO 2025</title>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;Data showed improvements across several key measures of visual function, including low luminance visual acuity and microperimetry&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Laru-zova was generally well-tolerated by DAWN participants at 6 months&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;LONDON and CAMBRIDGE, Mass., May  06, 2025  (GLOBE NEWSWIRE) -- Beacon Therapeutics Holdings Limited (‘Beacon Therapeutics’ or ‘the Company’), a leading clinical-stage biotechnology company with a mission to save and restore the vision of patients with blinding retinal diseases, today announced 6-month interim safety and efficacy results from the Phase 2 DAWN trial of the Company’s lead program, laru-zova (laruparetigene zovaparvovec), in patients with X-linked retinitis</description>
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   <title>Beacon Therapeutics Announces Positive Phase 2 Interim 6-Month Data from DAWN Trial of Laru-zova in Patients with X-linked Retinitis Pigmentosa (XLRP) at ARVO 2025</title>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;Data showed improvements across several key measures of visual function, including low luminance visual acuity and microperimetry&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Laru-zova was generally well-tolerated by DAWN participants at 6 months&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;LONDON and CAMBRIDGE, Mass., May  06, 2025  (GLOBE NEWSWIRE) -- Beacon Therapeutics Holdings Limited (‘Beacon Therapeutics’ or ‘the Company’), a leading clinical-stage biotechnology company with a mission to save and restore the vision of patients with blinding retinal diseases, today announced 6-month interim safety and efficacy results from the Phase 2 DAWN trial of the Company’s lead program, laru-zova (laruparetigene zovaparvovec), in patients with X-linked retinitis</description>
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   <title>Beacon Therapeutics Announces Positive Phase 2 Interim 6-Month Data from DAWN Trial of Laru-zova in Patients with X-linked Retinitis Pigmentosa (XLRP) at ARVO 2025</title>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;Data showed improvements across several key measures of visual function, including low luminance visual acuity and microperimetry&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Laru-zova was generally well-tolerated by DAWN participants at 6 months&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;LONDON and CAMBRIDGE, Mass., May  06, 2025  (GLOBE NEWSWIRE) -- Beacon Therapeutics Holdings Limited (‘Beacon Therapeutics’ or ‘the Company’), a leading clinical-stage biotechnology company with a mission to save and restore the vision of patients with blinding retinal diseases, today announced 6-month interim safety and efficacy results from the Phase 2 DAWN trial of the Company’s lead program, laru-zova (laruparetigene zovaparvovec), in patients with X-linked retinitis</description>
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   <title>Beacon Therapeutics Announces Positive Phase 2 Interim 6-Month Data from DAWN Trial of Laru-zova in Patients with X-linked Retinitis Pigmentosa (XLRP) at ARVO 2025</title>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;Data showed improvements across several key measures of visual function, including low luminance visual acuity and microperimetry&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Laru-zova was generally well-tolerated by DAWN participants at 6 months&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;LONDON and CAMBRIDGE, Mass., May  06, 2025  (GLOBE NEWSWIRE) -- Beacon Therapeutics Holdings Limited (‘Beacon Therapeutics’ or ‘the Company’), a leading clinical-stage biotechnology company with a mission to save and restore the vision of patients with blinding retinal diseases, today announced 6-month interim safety and efficacy results from the Phase 2 DAWN trial of the Company’s lead program, laru-zova (laruparetigene zovaparvovec), in patients with X-linked retinitis</description>
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   <title>Beacon Therapeutics Announces Positive Phase 2 Interim 6-Month Data from DAWN Trial of Laru-zova in Patients with X-linked Retinitis Pigmentosa (XLRP) at ARVO 2025</title>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;Data showed improvements across several key measures of visual function, including low luminance visual acuity and microperimetry&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Laru-zova was generally well-tolerated by DAWN participants at 6 months&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;LONDON and CAMBRIDGE, Mass., May  06, 2025  (GLOBE NEWSWIRE) -- Beacon Therapeutics Holdings Limited (‘Beacon Therapeutics’ or ‘the Company’), a leading clinical-stage biotechnology company with a mission to save and restore the vision of patients with blinding retinal diseases, today announced 6-month interim safety and efficacy results from the Phase 2 DAWN trial of the Company’s lead program, laru-zova (laruparetigene zovaparvovec), in patients with X-linked retinitis</description>
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   <title>Beacon Therapeutics Announces Positive Phase 2 Interim 6-Month Data from DAWN Trial of Laru-zova in Patients with X-linked Retinitis Pigmentosa (XLRP) at ARVO 2025</title>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;Data showed improvements across several key measures of visual function, including low luminance visual acuity and microperimetry&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Laru-zova was generally well-tolerated by DAWN participants at 6 months&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;LONDON and CAMBRIDGE, Mass., May  06, 2025  (GLOBE NEWSWIRE) -- Beacon Therapeutics Holdings Limited (‘Beacon Therapeutics’ or ‘the Company’), a leading clinical-stage biotechnology company with a mission to save and restore the vision of patients with blinding retinal diseases, today announced 6-month interim safety and efficacy results from the Phase 2 DAWN trial of the Company’s lead program, laru-zova (laruparetigene zovaparvovec), in patients with X-linked retinitis</description>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;Data showed improvements across several key measures of visual function, including low luminance visual acuity and microperimetry&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;center&quot;&gt;&lt;em&gt;Laru-zova was generally well-tolerated by DAWN participants at 6 months&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;LONDON and CAMBRIDGE, Mass., May  06, 2025  (GLOBE NEWSWIRE) -- Beacon Therapeutics Holdings Limited (‘Beacon Therapeutics’ or ‘the Company’), a leading clinical-stage biotechnology company with a mission to save and restore the vision of patients with blinding retinal diseases, today announced 6-month interim safety and efficacy results from the Phase 2 DAWN trial of the Company’s lead program, laru-zova (laruparetigene zovaparvovec), in patients with X-linked retinitis</description>
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   <title>Beacon Therapeutics Announces Positive Phase 2 Interim 6-Month Data from DAWN Trial of Laru-zova in Patients with X-linked Retinitis Pigmentosa (XLRP) at ARVO 2025</title>
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