News

A major trial of a promising gene therapy for Duchenne muscular dystrophy has fallen short, but researchers say the lessons learned could pave the way for better, more effective treatments.
Global Duchenne Muscular Dystrophy Drugs Market value attained USD 3.9 Billion in 2025. The market will achieve USD 6.5 ...
Health Secretary Neil Gray has been criticised for posting about football and traffic lights on social media while failing to ...
A new article argues dystrophin immunogenicity is an under-examined issue in the treatment of Duchenne muscular dystrophy.
Kye Pharmaceuticals, Inc. ("Kye") announced today it has submitted a New Drug Submission (NDS) to Health Canada for the ...
Suneel Ram's caregivers share some of the lessons they have learned while caring for the 28-year-old who was diagnosed with ...
DMD was first described by French neurologist Guillaume Benjamin Amand Duchenne in the 1860s. However, until the 1980s, ...
None of the eteplirsen-treated patients reached a left ventricular ejection fraction below 50% compared with 22.1% of ...
Doing more to incorporate caregiver burden into value assessments and cost-effectiveness research of Duchene muscular dystrophy treatments was the focus of a recent International Society for ...
Zydus Lifesciences has secured final approval from the US Food and Drug Administration (USFDA) to manufacture Jaythari (Deflazacort) tablets in four strengths - 6 mg, 18 mg, 30 mg, and 36 mg.
Patients in Scotland can't get the treatment - which is available in England - despite manufacturers giving it away for free ...
Suneel Ram is a spiritual seeker, sings in a band and was the subject of a comic novel two years ago about living with Duchenne muscular dystrophy, a rare genetic ...