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News for Healthier Living
Breakthrough Gene Therapy Shows Hope for Treating Fatal Childhood Leukodystrophy
Myrtelle Inc. ("Myrtelle"), a pioneering clinical-stage gene therapy company developing transformative treatments for neurodegenerative diseases, today announced the publication of interim results in Nature Medicine from a pioneering clinical study , reporting by researchers the first-in-human application of a gene therapy designed to restore myelin in the brains of children affected by Canavan Disease (CD), a rare and fatal pediatric leukodystrophy. The investigational treatment, known as MYR-101, uses a novel viral vector (rAAV-Olig001) with unique tropism for oligodendrocytes, the brain's myelin- producing cells.
September 16, 2025
September 16 2025September 15 2025 - CRF and the Jon DeHaan Foundation to Launch TCT AI Lab at TCT 2025
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- Texas A&M expands scientific access to biodiversity data
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- First-of-Its-Kind Study Links Gut Hormone GLP-1 to Brain Inflammation in Neurological Disorder
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Miss Out on Specialist Care During Pregnancy, Study Finds
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September 14 2025September 13 2025September 12 2025September 11 2025September 10 2025September 9 2025September 8 2025September 7 2025September 6 2025September 5 2025September 4 2025 - MSU Study Finds Accessible Wireless Ultrasounds Are Accurate
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September 3 2025 - Rutgers and RWJBarnabas Health Study Finds Pocket Ultrasound Reduces Hospital Stays for Patients with Shortness of Breath
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- Kathy Coleman Commits Additional $3.5 Million to Fuel the Future of Clinical Trials at University Hospitals Seidman Cancer Center
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September 2 2025 - Researchers Find Medicaid Is Crucial to Access Treatment for Opioid Addiction
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