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Benitec Biopharma Announces Acceptance of Late- Breaking Abstract for the BB-301 Phase 1b/2a Clinical Treatment Study at the Muscular Dystrophy Association Clinical & Scientific Conference
23 Feb 2026 12:00 GMT
… presentation at the 2026 Muscular Dystrophy Association Clinical & … Treatment Study ongoing in Oculopharyngeal Muscular Dystrophy Patients (OPMD) with … threatening human conditions including Oculopharyngeal Muscular Dystrophy (OPMD). A comprehensive …
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Battling pneumonia, muscular dystrophy, gritty Chandigarh teen arrives on stretcher to take Class 12 exam
21 Feb 2026 04:14 GMT
… Bisht, a student living with muscular dystrophy since birth, showed extraordinary grit … , Manimajra, on Friday. (HT Photo)
Muscular dystrophy is a genetic disorder that …
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Battling pneumonia, muscular dystrophy, student arrives on stretcher to take exam
20 Feb 2026 13:31 GMT
… Bisht, a student living with muscular dystrophy since birth, arrived at her … , 17, a student living with muscular dystrophy since birth, arrived at her …
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Firefighters braving freezing temperatures to raise money for Muscular Dystrophy Canada
19 Feb 2026 22:13 GMT
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CITGO Refinery Raises $234,000 for Muscular Dystrophy Association
19 Feb 2026 08:09 GMT
… recently hosted its 15th Annual Muscular Dystrophy Association (MDA) bowling event, raising … fuel MDA’s mission.
“The Muscular Dystrophy Association deeply values our longstanding …
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Sarepta Hits Fresh Hurdle As Court Revives Patent Lawsuit With Regenxbio Over Muscular Disorder Therapy
21 Feb 2026 01:55 GMT
… ) regarding the latter’s Duchenne muscular dystrophy (DMD) treatment.
According to a … developed treatments for DMD. Duchenne muscular dystrophy (DMD) is a severe, progressive …
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REGENXBIO Secures Legal Win in Gene Therapy Patent Battle vs. Sarepta
23 Feb 2026 14:12 GMT
… latter used for its Duchenne muscular dystrophy gene therapy.
The decision overturns … in June 2023 for Duchenne muscular dystrophy.
In January 2024, a Delaware …
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Wave Life Sciences to Present at Oppenheimer 36th Annual Healthcare Life Sciences Conference
23 Feb 2026 13:30 GMT
… includes clinical programs in Duchenne muscular dystrophy and Huntington’s disease, as …
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People with rare genetic conditions are ‘systematically ignored’ by NHS
23 Feb 2026 13:07 GMT
… as Williams syndrome and Duchenne muscular dystrophy, affect more than 3.5 …
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The New England Journal of Medicine Publishes Results from Phase 1/2 MARINA® Trial of Delpacibart Etedesiran (del-desiran) for Treatment of Myotonic Dystrophy Type 1
18 Feb 2026 22:38 GMT
… Oligonucleotide Conjugate for Myotonic Dystrophy Type 1."
DM1 … NCT05027269.
About Myotonic Dystrophy Type 1
Myotonic dystrophy type 1 (DM1) … 1 (DM1), Duchenne muscular dystrophy (DMD) and facioscapulohumeral muscular dystrophy (FSHD). Avidity is …