AccurKardia has gained the US Food and Drug Administration's (FDA) breakthrough device designation for its AI-powered ‘AK+ ...

Blue Ridge Beef is recalling 1,350 pounds of its raw cat food sold across the Northeast and mid-Atlantic after the product ...

WATERTOWN, Mass., Jan. 08, 2025 (GLOBE NEWSWIRE) -- Vigil Neuroscience, Inc. (Nasdaq: VIGL), a clinical-stage biotechnology ...

Text message-based programming and the drug varenicline were the only 2 strategies that were shown to be effective for quitting vaping.

Investigational new drug (IND) applications for initiating first-in-human studies for ZW220 and ZW251 in solid tumors anticipated in 2025IND applications for initiating first-in-human studies for ZW20 ...

“The proposed rule, Tobacco Product Standard for Nicotine Level of Certain Tobacco Products, is displaying in the Office of ...

A database of medical device reports shows a patient enrolled in a Varipulse study had a stroke shortly after treatment. Read ...

LUMRYZ, is an extended-release sodium oxybate medication approved by the FDA on May 1, 2023, as the first and only once-at-bedtime treatment for cataplexy or excessive daytime sleepiness (EDS) in ...

Democratic lawmakers in Washington are pushing this year to ban flavored tobacco products, with the support of the state ...

The temporary halt to investigate reported neurovascular events comes two months after Johnson & Johnson won FDA approval for ...

The FDA is adding a warning about Guillain-Barré syndrome to the respiratory syncytial virus vaccines manufactured by GSK and ...

DBV Technologies Announces Positive 3-Year Results from EPITOPE Phase 3 Open-Label Extension Study EPITOPE OLE data ...