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FDA approves higher dose of Catalyst's LEMS drug By Investing.com
Investing.com· 13 hours agoCatalyst Pharmaceuticals, Inc. (NASDAQ: CPRX), a commercial-stage biopharmaceutical company,...
FDA Conditionally Approves Eli Lilly's Thyroid Cancer Drug For Pediatric Patients With Certain...
Benzinga via Yahoo Finance· 1 day agoWednesday, the FDA granted accelerated approval to Eli Lilly And Co’s (NYSE:LLY) selpercatinib...
FDA approves Teva Pharmaceuticals’ AUSTEDO XR for TD and HD chorea
Pharmaceutical Technology via Yahoo Finance· 21 hours agoThe US Food and Drug Administration (FDA) has approved Teva Pharmaceuticals’ AUSTEDO XR...
FDA approves Beckman Coulter’s assay to assess heart failure
Medical Device Network via Yahoo Finance· 20 hours agoThe US Food and Drug Administration (FDA) has approved clinical diagnostics company Beckman...
FDA Approves Nonstimulant Liquid Onyda XR for ADHD
Medscape· 1 day agoThe centrally acting alpha2-adrenergic agonist allows for nighttime dosing and can be used with stimulants, the drug's manufacturer says.
Is Compounded Ozempic Safe For Weight Loss? What You Need To Know
Forbes· 3 days agoWeight-loss treatments like semaglutide (Ozempic) and tirzepatide (Mounjaro) have been life changing...
Small Business - The Brewton Standard | The Brewton Standard
The Brewton Standard· 3 hours agoU.S. FDA ACKNOWLEDGES ASTELLAS' RESUBMISSION OF BIOLOGICS LICENSE APPLICATION FOR ZOLBETUXIMAB AND SETS NEW ACTION DATE PR Newswire TOKYO, May 30, 2024 If approved ...
FDA grants IND clearance for Spinogenix’s ALS treatment trial
Clinical Trials Arena via Yahoo Finance· 20 hours agoSPG302 has also been recognised by the FDA as an orphan drug for ALS treatment. It previously...
FDA approves Amgen’s interchangeable biosimilar Bkemv
Pharmaceutical Technology via Yahoo Finance· 2 days agoThe US Food and Drug Administration (FDA) has approved Amgen's Bkemv (eculizumab-aeeb) as the first...
Small Business - The Roanoke-Chowan News-Herald | The Roanoke-Chowan News-Herald
Roanoke-Chowan News-Herald· 2 hours agoThe US Food and Drug Administration (FDA) has extended by three months the target action date of its priority review of the supplemental Biologics License ...