Tag: Duchenne muscular dystrophy

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Recent Related Articles to Duchenne muscular dystrophy

Sarepta Stock Slumps After EU Regulator Recommends Refusing Approval To Its ... - Stocktwits

Added to Collection on: 2025-07-26 20:21:13

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Biotechnology
Corvallis, Oregon
Sarepta Therapeutics
Muscular dystrophy
Delandistrogene moxeparvovec
Applied genetics
Duchenne muscular dystrophy
Gene therapy
StockTwits
Duchenne
Dystrophy
Roche
United States

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FDA allows Sarepta to resume some Elevidys shipments - BioPharma Dive

Added to Collection on: 2025-07-29 09:38:40

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Biotechnology
Muscular dystrophy
Corvallis, Oregon
Sarepta Therapeutics
Rare diseases
Delandistrogene moxeparvovec
Duchenne muscular dystrophy
Genetic engineering
Gene therapy
Duchenne

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Sarepta Shares Surge 10.46% on Record Q2 Revenue Despite Safety Scrutiny Trading ...

Added to Collection on: 2025-08-07 23:06:05

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Biotechnology
Molecular biology
Corvallis, Oregon
Sarepta Therapeutics
Delandistrogene moxeparvovec
Applied genetics
Gene therapy
Duchenne muscular dystrophy
Roche
Small interfering RNA

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Sarepta Soars on Q2 Earnings & Sales Beat, Resumes Elevidys Deliveries - TradingView

Added to Collection on: 2025-08-07 14:44:38

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Muscular dystrophy
Biotechnology
Rare diseases
Antisense RNA
Morpholines
Sarepta Therapeutics
Delandistrogene moxeparvovec
Duchenne muscular dystrophy
Gene therapy
Limb–girdle muscular dystrophy
Roche
Casimersen
Sarepta Therapeutics Inc.

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Elevidys sales weaken; Neumora gets into obesity - BioPharma Dive

Added to Collection on: 2025-08-09 01:11:47

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Biotechnology
Novo Nordisk
Applied genetics
Corvallis, Oregon
Sarepta Therapeutics
Delandistrogene moxeparvovec
Gene therapy
Duchenne muscular dystrophy
Pfizer
Familial amyloid polyneuropathy

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Vinay Prasad, in surprise reversal, to rejoin FDA after abrupt departure | BioPharma Dive

Added to Collection on: 2025-08-09 18:52:18

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Biotechnology
Marty Makary
Center for Biologics Evaluation and Research
Delandistrogene moxeparvovec
Peter Marks
Sarepta Therapeutics
Vinay Prasad
Food and Drug Administration
Laura Loomer
Duchenne muscular dystrophy
Gene therapy
Biopharmaceutical

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Avidity Biosciences Completes $690 Million Share Offering - AInvest

Added to Collection on: 2025-09-15 20:24:34

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Muscular dystrophy
Rare diseases
Nucleic acids
Dystrophy
Medical terminology
DM1
Duchenne muscular dystrophy
Oligonucleotide
Facioscapulohumeral muscular dystrophy
Biotechnology
Duchenne
Avidity Biosciences Inc.

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Health Canada approves Santhera's Agamree for DMD treatment

Added to Collection on: 2025-10-06 07:39:34

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Muscular dystrophy
Rare diseases
Duchenne muscular dystrophy
Vamorolone
Catalyst Pharmaceuticals
DMD
Priority review
Dystrophin
Prosensa

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$AISP stock is up 16% today. Here's what we see in our data.

Added to Collection on: 2025-10-06 15:13:12

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Rare diseases
Myotonia
Myotonic dystrophy
Muscular dystrophy
Dystrophy
Duchenne muscular dystrophy
DM1
Myotonin-protein kinase
Glycogen storage disease type II

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Immix Biopharma, Inc. to Present NXC-201 Abstract at ASH 67th Annual Meeting

Added to Collection on: 2025-10-06 20:46:43

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Rare diseases
Myotonia
Myotonic dystrophy
Muscular dystrophy
Dystrophy
Duchenne muscular dystrophy
DM1
Myotonin-protein kinase
Glycogen storage disease type II

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