Biogen beat Q4 estimates with a 17% EPS rise and $2.46 billion in sales. The company expects revenue declines in 2025 as multiple sclerosis drug sales drop.
AB-1002 is an investigational gene therapy for the treatment of adults with non-ischemic cardiomyopathy and New York Heart Association (NYHA) Class III heart failure symptoms GenePHIT is a clinical ...
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Hosted on MSNLundbeck gains FDA fast track designation for MSA therapy amlenetugThe designation will provide Lundbeck with the possibility of rolling reviews and detailed guidance to streamline the drug ...
AB-1002 is an investigational gene therapy for the treatment of adults with non-ischemic cardiomyopathy and New York Heart Association (NYHA) ...
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Hosted on MSNBiogen's Q4 Earnings & Sales Beat, 2025 EPS Guidance DisappointsBiogen BIIB reported fourth-quarter 2024 adjusted earnings per share (EPS) of $3.44, which beat the Zacks Consensus Estimate of $3.42. Earnings rose 17% year over year on a reported basis, boosted by ...
The 5 mg risdiplam tablet provides the same efficacy and safety for spinal muscular atrophy as the currently available oral ...
We've all experienced it: you're in the middle of a conversation, searching for a word, a name, or a title, and… nothing. You know you know it—you can almost feel it—but it just won't come. This ...
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A team of researchers from the Sant Pau Research Institute (IR Sant Pau) has published a study in the Journal of ...
More than one million people are receiving between £28.70 and £184.30 each week through PIP or Adult Disability Payment for ...
Over the past nine years, patients with spinal muscular atrophy have seen the number of FDA-approved treatment options for ...
FDA Approves Genentech’s Evrysdi Tablet as First and Only Tablet for Spinal Muscular Atrophy (SMA)
SOUTH SAN FRANCISCO, CA, USA I 12, 2025 I Genentech, a member of the Roche Group (SIX: RO, ROG; OTCQX: RHHBY), announced today that the U.S. Food and Drug Administration (FDA) has approved a New Drug ...
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