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Neuromuscular Disease News
Top neuro stories of December: Sunlight may lower MS risk in kids, FDA approves Vyvgart
Healio Neurology’s five most-viewed stories in December highlight a study on increased sun exposure lowering children’s MS risk, FDA approval of a treatment for myasthenia gravis and research on a self-administered examination that may quickly identify mild cognitive impairment conversion to dementia.
Merck to acquire rights to develop cladribine for myasthenia gravis, NMOSD
Merck announced it has entered an agreement to acquire Chord Therapeutics, a biotech company that focuses on rare neuroinflammatory diseases, to expand its neurology pipeline.
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FDA approves Vyvgart for treatment of myasthenia gravis
The FDA announced the approval of Vyvgart for treatment of the chronic autoimmune, neuromuscular disease myasthenia gravis in adults who are positive for acetylcholine receptor antibody.
Rituximab may not significantly reduce steroid use in form of myasthenia gravis
Although rituximab was safe and well tolerated in acetylcholine receptor antibody-positive generalized myasthenia gravis, researchers noted low probability of it significantly reducing steroid use at 1 year.
Kids who get more sunlight may have lower risk for MS
Increased sunlight exposure may offer significant protection against development of pediatric MS, according to study results published in Neurology.
Blackrock Neurotech gets FDA breakthrough designation for immobility intervention
The FDA has granted breakthrough device designation to Blackrock Neurotech for its MoveAgain Brain Computer Interface System, according to a company press release.
Limited mobility, activity typically seen with limb girdle muscular dystrophy
Survey data provided insight into the symptomatic burden of limb girdle muscular dystrophy, according to study results published in Neuromuscular Disorders.
Among activity types, moderate exercise provides best ALS protection
Lifetime physical activity did not appear to increase risk for ALS, whereas occupational physical activity seemed to be a risk factor for the disease, according to study results published in Neurology.
Biogen to launch study of higher Spinraza dose in patients with later onset SMA
Biogen announced it intends to initiate a global phase 3b study to investigate clinical outcomes and safety of a higher dose of Spinraza in patients with later onset spinal muscular atrophy previously treated with Evrysdi.
Translarna delays ambulation loss in boys with Duchenne muscular dystrophy
PTC Therapeutics Inc. released results showing that treatment with Translarna delayed loss of ambulation by more than 5 years among boys with nonsense mutation Duchenne muscular dystrophy vs. standard of care alone.
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Headline News
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Headline News
A potential new paradigm for treating acute migraine: Timolol nasal spray
November 15, 20245 min read -
Headline News
AI-enabled video of skin on face, hands may detect high blood pressure, diabetes
November 15, 20242 min read -
Headline News
‘Troubling’ data show lack of awareness about lung cancer screening
November 15, 20242 min read