Alzheimer’s disease affects more than 30m people worldwide, mostly the elderly. After the age of 65, the chance of developing ...
Thousands of web pages have been scrubbed from government websites, but nothing on the internet is truly ever gone.
The FDA on Tuesday signed off on Supernus Pharmaceuticals’ apomorphine hydrochloride injection—to be marketed under the brand ...
Acrivon Therapeutics said the Food and Drug Administration has granted Breakthrough Device designation for its ACR-368 OncoSignature assay, an immunofluorescence assay for the identification of ...
Acrivon Therapeutics (ACRV) announced the U.S. Food and Drug Administration, FDA, has granted Breakthrough Device designation, BDD, for the ...
The company has recalled the two-pound bags of its Natural Mix that were sold in eight states after a sample tested positive ...
Vertex Pharmaceuticals ( VRTX 2.53%) has long been known as the company to turn to for life-saving cystic fibrosis (CF) drugs ...
Robert F. Kennedy, Jr. has no training in health care, public health, global health issues, or drug and vaccine safety, writes. He does have lots of opinions, however, and these opinions could shape ...
The Food and Drug Administration has upgraded its classification of a broccoli recall initially reported in late December, ...
Wong, Founder and CEO of HCW Biologics, commented, “The FDA’s clearance to initiate our first-in-human clinical trial for HCW9302 brings us one step closer to advancing a potentially transformative ...
The Food and Drug Administration announced it would decide ... but many include ingredients that can release formaldehyde when heated, the FDA said in 2024. Over the years, an increasing number ...
The U.S. Food and Drug Administration (FDA) approved suzetrigine under the brand name Journavx on Jan. 30, 2025. Journavx is a first-in-class non-opioid painkiller that acts on sodium channels in the ...