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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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GNR-097: Duchenne Gene Therapy Phase 1/2 Study Started by Generium

Research 0
Generium is a Russian innovative biotechnology company has received...

How Does My Child Participate in Clinical Trials for Duchenne?

DMD 0
If your child has been diagnosed with Duchenne muscular...

SQY Therapeutics Receives Orphan Drug Designation from the European Medicines Agency for Exon 51 Skipping Therapy SQY51 for Treatment of Duchenne Muscular Dystrophy

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SQY51 had already obtained Orphan Drug Designation from the...

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Frequently Asked Questions About Elevidys Used for Duchenne Muscular Dystrophy

Approved Treatments 5
A genetic condition known as Duchenne muscular dystrophy (DMD)...

Potential Upcoming New Gene Therapies for Duchenne Muscular Dystrophy

Research 7
The results of new gene therapy studies for Duchenne...

Duchenne Muscular Dystrophy: Treatment & Cost

Editorials 1
The excitement you feel until your child is born...

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