FDA lifts clinical hold on Intellia's CRISPR Phase 3 trial
Intellia Therapeutics (NASDAQ:NTLA) announced today that the U.S. Food and Drug Administration (FDA) has removed the clinical hold on its MAGNITUDE-2 Phase 3 clinical trial.
Intellia Therapeutics (NASDAQ:NTLA) announced today that the U.S. Food and Drug Administration (FDA) has removed the clinical hold on its MAGNITUDE-2 Phase 3 clinical trial.
HCA Healthcare (NYSE:HCA) delivered a powerful finish to 2025, reporting a 30.6% surge in fourth-quarter net income as the largest U.S. hospital operator capitalized on rising patient demand and stabilized labor costs.
UnitedHealth Group (NYSE:UNH) announced its full-year 2025 results on Tuesday, reporting consolidated revenues of $447.6 billion—a 12% increase year-over-year.
Neurocrine Biosciences (NASDAQ:NBIX) announced on January 26, 2026, the initiation of its Phase 2 clinical study for NBI-1065890, an investigational compound targeting tardive dyskinesia (TD).
Milestone Pharmaceuticals (NASDAQ:MIST) has officially moved into the commercial stage with the U.S. retail launch of Cardamyst™ (etripamil).
SciSparc (NASDAQ:SPRC), a company traditionally focused on cannabinoid-based pharmaceuticals, has officially pivoted into the medical device sector.
Mirum Pharmaceuticals (NASDAQ:MIRM) announced the successful closing of its acquisition of Bluejay Therapeutics, a move that significantly broadens its rare disease pipeline with a potential first-in-class therapy for chronic hepatitis delta virus (HDV).
United Therapeutics (NASDAQ:UTHR) has cleared a primary safety hurdle in its ambitious effort to manufacture biological alternatives to human organs, reporting that its bioengineered external liver supported critically ill patients without serious adverse effects.
MannKind (NASDAQ:MNKD) received U.S. Food and Drug Administration approval on Monday for a critical update to the prescribing information for Afrezza, its inhaled mealtime insulin.
Biogen (NASDAQ:BIIB) and Eisai have cleared a significant regulatory hurdle as the U.S. Food and Drug Administration (FDA) accepted their supplemental Biologics License Application for a subcutaneous version of the Alzheimer’s treatment Leqembi.
Bausch Health Companies (NYSE:BHC) today announced results from its global Phase 3 RED-C clinical program evaluating amorphous-rifaximin SSD for the primary prevention of hepatic encephalopathy (HE) in adults with liver cirrhosis.
Sanara MedTech (NASDAQ:SMTI) announced preliminary unaudited financial results for the fourth quarter and full year ended December 31, 2025, along with initial guidance for 2026.