WASHINGTON (AP) — Shortly before he was forced to resign, the nation’s top vaccine regulator says he refused to grant Health ...

With its FDA approval for specific mutations in the RPE65 gene ... LUXTURNA uses an adeno-associated viral type 2 (AAV2) vector to deliver the RPE65 gene. The vector includes a cytomegalovirus (CMV) ...

As an unintended benefit, extending the use of nitisinone as a vector control tool could consequently increase drug ...

But the Food and Drug Administration is phasing in bans on compounded copies of the brand names, with the latest step taking effect Wednesday. Jessica Baylis, 44, of Greenlawn, who has lost nearly ...

The drug, tested on mice, restored these gamma oscillations, and in turn reconnected neurons to essentially heal the brain damage without arduous physical rehabilitation.

The U.S. Food and Drug Administration unveiled the Chemical Contaminants Transparency Tool (CCT Tool), an online searchable database providing a consolidated list of contaminant levels (e.g., ...

The FDA has again refused to provide information about the deadly 2024 E. coli O157 outbreak traced to romaine lettuce. Although the Food and Drug Administration knew what grower and distributor ...

Court documents released Tuesday offered few glimpses into Prince Harry's entrance to the U.S., as federal officials argued that the royal would suffer needless "harm" and "harassment" if detailed ...

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The team found that the U.S. Food and Drug Administration (FDA)-approved drug sevelamer, typically prescribed to help bind excess phosphorus in the blood of people with chronic kidney disease ...