GM1 Treatment PBGM91 Shows Positive Interim Data in Phase 1/2, Additional Cohorts Planned
December 22nd 2021Two patients with late infantile GM1 gangliosidosis in Cohort 1 received a low dose of the treatment, reporting no serious adverse events. Passage Bio noted it plans to move forward with 2 additional cohorts.
DAPT Approach With Ticagrelor, Clopidogrel Demonstrate Efficacy Over Aspirin Alone
December 21st 2021Although similar in reducing the risk of recurrent stroke, the use dual antiplatelet therapy with clopidogrel and aspirin was associated with a decreased risk of functional disability compared with ticagrelor and aspirin.
Biogen Announces 50% Drop in Aducanumab Pricing Amid Feedback on Costs
December 20th 2021After months of concern raised by the Alzheimer disease community about the list price for aducanumab (Aduhelm) of $56,000 yearly, Biogen has announced that the maintenance dose cost will be reduced to $28,200.
Treatment Optimization of Antiseizure Medications, Holding Higher Standards: William Rosenfeld, MD
December 19th 2021The neurologist from the Comprehensive Epilepsy Care Center for Children and Adults, in St. Louis, Missouri, provided context on improving our use of current antiseizure medications as the top priority for patients with epilepsy. [WATCH TIME: 2 minutes]
Outlining the Clinical and Radiological Features of NMOSD, MOGAD
December 18th 2021Amy Kunchok, MD, staff neurologist at the Mellen Center for Multiple Sclerosis and Research at Cleveland Clinic, discussed a recent talk she gave that highlighted the different phenotypes of AQP-IgG NMOSD and MOGAD.
Clinical, Radiological Features of NMOSD and MOGAD: Amy Kunchok, MD
December 16th 2021The staff neurologist at the Cleveland Clinic Mellen Center for Multiple Sclerosis outlined key findings from her talk at a recent Institutional Perspectives in Neurology: Multiple Sclerosis event. [WATCH TIME: 3 minutes]
Biogen and Eisai Offer Update on Phase 4 Post-Marketing Aducanumab Study
December 16th 2021The post-marketing study of aducanumab (Aduhelm) is expected to enroll 1300 patients with early Alzheimer, with the final protocol to be submitted to the FDA in March 2022, and plans to initiate patient screening in May 2022.