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We do not want children to die from a disease that can be cured. We want to give hope to families and ensure that all children with DMD are treated and regain their health.

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Avidity Biosciences Prepares for Three Rare Muscle Disease Programs’ 2025 BLA Submission and Commercialization

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A biopharmaceutical firm dedicated to developing a novel class...

What is Agamree (vamorolone)? What is Agamree Used For?

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We will answer your questions such as what is...

Turkish DMD Patients Who are Eligible for Exon 51 Skipping Treatment Request Their Medications from the Ministry of Health

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The DMD Dayanisma Community, founded by families of children...

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Frequently Asked Questions About Elevidys Used for Duchenne Muscular Dystrophy

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A genetic condition known as Duchenne muscular dystrophy (DMD)...

Capricor Therapeutics Submits Application for Treatment of DMD Cardiomyopathy

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Capricor Therapeutics, a biotechnology company developing transformative cell and...

Cures of Duchenne (List of All Researches)

Research 2
Dystrophin Gene Therapy MechanismCompanyDrugStatus Micro-dystrophin Gene Replacement Sarepta TherapeuticsElevidys/SRP-9001ApprovedMicro-dystrophin Gene ReplacementPfizerPF-06939926DiscontinuedMicro-dystrophin Gene...

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