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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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INS1201 Gene Therapy Phase 1 Clinical Trial Begins

Research 0
Insmed was announced on the page published on ClinicalTrials.gov...

Sarepta to Lay Off About 500 Employees After Duchenne Gene Therapy Setbacks

Press Releases 0
Sarepta stated that company intends to halt development on...

Precision BioSciences Highlights New Preclinical Data for PBGENE-DMD for the Treatment of Duchenne Muscular Dystrophy

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Precision BioSciences a clinical stage gene editing company utilizing...

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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 5
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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