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Neurorehabilitation News
FDA approves injectable for subcutaneous use in adults with generalized myasthenia gravis
Halozyme Therapeutics announced that argenx received FDA approval for Vyvgart Hytrulo with Enhanze for subcutaneous use in adults with generalized myasthenia gravis who are anti-acetylcholine receptor antibody positive.
Venous manometry could aid idiopathic intracranial hypertension diagnosis
AUSTIN, Texas — Venous manometry and neuroimaging may provide additional value when diagnosing patients who do not meet criteria for idiopathic intracranial hypertension, according to a poster presented here.
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FDA grants orphan drug designation to RNA therapy for Charcot-Marie-Tooth disease type 1A
The FDA has granted orphan drug designation to DTx-1252, an investigational small interfering RNA therapeutic to treat Charcot-Marie-Tooth disease type 1A.
Ketamine may be effective modulator for suicide-related cognition in adults
MIAMI BEACH, Fla. — Treatment with ketamine may be an effective augmenter of risk mitigation for suicidality and effective modulator for suicide-related cognitive processing in adults, according to data presented here.
AAN submits formal coverage reconsideration request to CMS for Alzheimer’s treatment
The American Academy of Neurology has submitted a formal national coverage determination reconsideration request to CMS regarding current coverage of amyloid-targeting monoclonal antibodies for Alzheimer’s disease, including Leqembi.
FDA clears OCD motor threshold cap for transcranial magnetic stimulation system
The FDA has granted 510(k) clearance to Neuronetics Inc. for its obsessive-compulsive disorder motor threshold cap technology for NeuroStar Advanced Therapy for Mental Health.
Phase 2 study of systemic pegcetacoplan for ALS fails to meet efficacy endpoints
Apellis Pharmaceuticals Inc. announced that its phase 2 MERIDIAN study investigating systemic pegcetacoplan as a treatment for ALS failed to meet efficacy measures of overall function, survival, lung function and muscle strength.
FDA grants MRI conditional use for implantable sleep apnea therapy
The FDA has granted conditional use with MRI to an implantable transvenous phrenic nerve stimulation therapy for adults with moderate to severe central sleep apnea.
VIDEO: BrainPath device reduced hematomas in most patients with intracerebral hemorrhages
BOSTON — The BrainPath device successfully surgically evacuated intracerebral hemorrhages in most patients enrolled in the ENRICH trial, Andrew Russman, DO, said in a Healio video during the American Academy of Neurology Annual Meeting.
Valbenazine well-tolerated, improved chorea associated with Huntington’s disease
Treatment with valbenazine at doses up to 80 mg once daily was generally well-tolerated and significantly improved chorea compared with placebo in adults with Huntington’s disease, according to research in The Lancet Neurology.
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Headline News
CDC confirms pediatric case of bird flu in California, first in US child
November 22, 20242 min read -
Headline News
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November 22, 20242 min read -
Headline News
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