FDA adds strongest warning to Sarepta gene therapy linked to 2 patient deaths

The Food and Drug Administration is adding a new warning to a gene therapy linked to two patient deaths earlier this year.

As infant botulism cases climb to 31, recalled ByHeart baby formula is still on some store shelves

At least 31 babies in 15 states who drank ByHeart formula have been hospitalized and treated for infantile botulism since ...

The FDA removes a long-standing warning from hormone-based menopause drugs

The Food and Drug Administration says it will remove a long-standing warning from hormone-based drugs used to treat menopause symptoms in women ...

NIH funding cuts have affected over 74,000 people enrolled in experiments, a new report says

NEW YORK (AP) — Over 74,000 people enrolled in experiments have been affected by the National Institutes of Health’s funding ...
Zacks Small Cap Research on MSN

ARWR: REDEMPLO® Approved by FDA for the Treatment of FCS…

ARWR READ THE FULL ARWR RESEARCH REPORT Business Update REDEMPLO® Approved by FDA On November 18, 2025, Arrowhead Pharmaceuticals, Inc. (NASDAQ:ARWR) announced that the U.S. Food and Drug ...
Australian Associated Press

icotec Receives FDA Clearance for the CMORE® CT System, Expanding its BlackArmor® Engineered Carbon/PEEK Technology to the Posterior Cervicothoracic Spine

icotec is excited for the upcoming commercial launch of the CMORE ® CT System in the United States. This system will expand icotec's portfolio of BlackArmor ® Engineered Carbon/PEEK implants designed ...