Approval of iohexol injection 350 mg iodine/mL in 50 mL, 75 mL and 100 mL vials, and 300 mg iodine/mL in 50 mL vial, significantly expands Amneal’s injectable contrast portfolioPortfolio now ...
The FDA has placed a partial clinical hold on Novartis’ recently-approved gene therapy Zolgensma for spinal muscular atrophy (SMA), after animal studies pointed to a possible risk with the drug. In a ...
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First participant dosed in Ionis’ Phase I-II ASCEND study
The open-label trial enrolled patients aged between two and 12 years who have a clinical diagnosis of Dravet syndrome.
Study examines Qalsody safety after approval “This study is the first to systematically conduct a post-marketing [safety] ...
Blood-brain barrier drug delivery reached a landmark: the FDA’s March 2026 accelerated approval of Denali Therapeutics’ ...
Investor's Business Daily on MSN
Biogen slumps as Alzheimer's study leaves 'more questions than answers'
Biogen and Ionis said Tuesday their tau-targeting Alzheimer's treatment slowed cognitive decline by 26% over the course of 18 months.
Ionis Pharmaceuticals, Inc. (Nasdaq: IONS) today announced that the first participant has been dosed in the Phase 1-2 ASCEND study of ION337, an investigational RNA-targeted medicine for people living ...
Biogen Inc. (NASDAQ:BIIB) traded higher after releasing encouraging Phase 2 data for its experimental Alzheimer’s treatment, ...
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Biogen backs Alzheimer's tau drug for phase 3 despite trial miss
MarketBeat Week in Review – 05/18 - 05/22 Biogen (NASDAQ:BIIB) said data from its Phase 2 CELIA study of diranersen in early ...
Alzheimer's Association International Conference (AAIC Meeting) 2026 July 12, 2026 11:15 AM EDTCompany ParticipantsTim Power - Head ...
The Phase I/II trial will enroll pediatric patients with the seizure-causing condition who will be dosed every six months.
Researchers are exploring delivering super-specific AAVs through the brain's natural waste disposal system, which can carry ...
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