<turbo-stream action="append" target="news"><template>  <div class="row mb-4 py-2 news-box">
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/en/stock/REGENXBIO-Inc-US75901B1070">REGENXBIO, Inc.</a></div>
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        <div class="me-2 text-gray">PRNewsWire</div>
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        <div class="me-2 text-gray">about 2 months ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.prnewswire.com/news-releases/regenxbio-reports-second-quarter-2026-financial-results-and-operational-highlights-302844662.html">REGENXBIO Reports Second Quarter 2026 Financial Results and Operational Highlights</a>
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        RGX-202 BLA submission for Duchenne muscular dystrophy on track for Q3 2026 initiation, with potential accelerated approval in 2H 2027 Long-term surabgene lomparvovec (sura-vec, ABBV-RGX-314) data highlight durable safety and efficacy profile ahead of key catalyst Topline data from pivotal subretinal wet AMD studies, ATMOSPHERE ® and ASCENT ®**, expected in Q4 2026 Phase IIb/III NAAVIGATE trial...
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/en/stock/REGENXBIO-Inc-US75901B1070">REGENXBIO, Inc.</a></div>
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        <div class="me-2 text-gray">2 months ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.prnewswire.com/news-releases/regenxbio-presents-positive-long-term-data-for-surabgene-lomparvovec-in-wet-amd-and-diabetic-retinopathy-at-american-society-of-retina-specialists-annual-meeting-302828998.html">REGENXBIO Presents Positive Long-Term Data for Surabgene Lomparvovec in Wet AMD and Diabetic Retinopathy at American Society of Retina Specialists Annual Meeting</a>
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        One-time gene therapy treatment with sura-vec demonstrated long-term efficacy at similar doses to those being evaluated in ongoing late-stage studies: Stable to improved vision through 5 years in wet AMD patients who required frequent anti-VEGF injections prior to one-time sura-vec; no drug-related IOI observed in a setting of no prophylactic steroids Prevention of vision-threatening events wit...
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/en/stock/REGENXBIO-Inc-US75901B1070">REGENXBIO, Inc.</a></div>
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        <div class="me-2 text-gray">2 months ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.prnewswire.com/news-releases/regenxbio-announces-pricing-of-public-offering-of-common-stock-and-pre-funded-warrants-302828273.html">REGENXBIO Announces Pricing of Public Offering of Common Stock and Pre-funded Warrants</a>
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        ROCKVILLE, Md., July 17, 2026 /PRNewswire/ -- REGENXBIO Inc. (Nasdaq: RGNX) today announced the pricing of an underwritten public offering of 10,003,889 shares of its common stock at the price of $9.00 per share and 1,111,111 pre-funded warrants at a price of $8.9999 per warrant, in each case before underwriting discounts and commissions.
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/en/stock/REGENXBIO-Inc-US75901B1070">REGENXBIO, Inc.</a></div>
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        <div class="me-2 text-gray">2 months ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.prnewswire.com/news-releases/regenxbio-announces-proposed-public-offering-of-common-stock-302827988.html">REGENXBIO Announces Proposed Public Offering of Common Stock</a>
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        ROCKVILLE, Md., July 16, 2026 /PRNewswire/ -- REGENXBIO Inc. (Nasdaq: RGNX) today announced that it intends to offer and sell, subject to market conditions, $100 million of its common stock in an underwritten public offering.
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/en/stock/REGENXBIO-Inc-US75901B1070">REGENXBIO, Inc.</a></div>
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        <div class="me-2 text-gray">3 months ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.prnewswire.com/news-releases/regenxbio-announces-first-patient-dosed-in-phase-iibiii-naavigate-trial-of-surabgene-lomparvovec-in-diabetic-retinopathy-company-to-receive-100-million-milestone-302812721.html">REGENXBIO Announces First Patient Dosed in Phase IIb/III NAAVIGATE Trial of Surabgene Lomparvovec in Diabetic Retinopathy; Company to Receive $100 Million Milestone</a>
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        New long-term data from diabetic retinopathy and wet AMD programs to be presented at American Society of Retina Specialists (ASRS) 2026 ROCKVILLE, Md., June 29, 2026 /PRNewswire/ -- REGENXBIO Inc. (Nasdaq: RGNX) today announced the first patient has been dosed in the Phase IIb/III NAAVIGATE clinical trial of investigational surabgene lomparvovec (sura-vec, ABBV-RGX-314) in diabetic retinopathy ...
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/en/stock/REGENXBIO-Inc-US75901B1070">REGENXBIO, Inc.</a></div>
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        <div class="me-2 text-gray text-size-10">●</div>
        <div class="me-2 text-gray">3 months ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.prnewswire.com/news-releases/regenxbio-completes-dosing-in-confirmatory-study-of-rgx-202-marking-completion-of-registrational-development-program-and-supporting-planned-bla-submission-in-q3-2026-302808616.html">REGENXBIO Completes Dosing in Confirmatory Study of RGX-202, Marking Completion of Registrational Development Program and Supporting Planned BLA Submission in Q3 2026</a>
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        Confirmatory study completed ahead of schedule due to strong patient demand and robust investigator interest On track to initiate BLA in Q3 2026 under the accelerated approval pathway supporting potential approval in 2H 2027 ROCKVILLE, Md., June 24, 2026 /PRNewswire/ -- REGENXBIO Inc. (Nasdaq: RGNX) today announced the successful completion of dosing in the confirmatory study of RGX-202, a pote...
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/en/stock/REGENXBIO-Inc-US75901B1070">REGENXBIO, Inc.</a></div>
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        <div class="me-2 text-gray text-size-10">●</div>
        <div class="me-2 text-gray">3 months ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.prnewswire.com/news-releases/regenxbio-announces-alignment-with-fda-on-path-forward-for-navsunli-bla-resubmission-for-accelerated-approval-first-potential-gene-therapy-for-mps-ii-302806010.html">REGENXBIO Announces Alignment with FDA on Path Forward for NAVSUNLI™ BLA Resubmission for Accelerated Approval; First Potential Gene Therapy for MPS II</a>
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        FDA confirmed no additional studies required, existing longer-term data from the CAMPSIITE ® study will be reviewed on an expedited basis for approval via the accelerated approval pathway The Company expects to resubmit the BLA in Q3 2026 ROCKVILLE, Md., June 22, 2026 /PRNewswire/ -- REGENXBIO Inc. (Nasdaq: RGNX) today announced it has aligned with the U.S. Food and Drug Administration (FDA) re...
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/en/stock/REGENXBIO-Inc-US75901B1070">REGENXBIO, Inc.</a></div>
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        <div class="me-2 text-gray">3 months ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.reuters.com/business/healthcare-pharmaceuticals/fda-reverse-rejection-regenxbios-rare-disease-drug-wsj-reports-2026-06-22/">FDA to reverse rejection of Regenxbio&#39;s rare-disease drug, WSJ reports</a>
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        The ​U.S. Food ‌and Drug ​Administration ​will reverse ⁠its ​earlier ​rejection of a ​rare-disease ​therapy from Regenxbio , ‌the ⁠Wall Street ​Journal ​reported ⁠on Monday.
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