LAS VEGAS, NV / ACCESS Newswire / July 18, 2025 / ALT5 Sigma Corporation (NASDAQ:ALTS)(FRA:5AR1) (“ALT5 or the “Company”), a ...

Sarepta Therapeutics Inc. has refused to pause all shipments of its Elevidys treatment after three deaths were linked to the ...

The U.S. Food and Drug Administration (FDA) announced on July 14, 2025, that it is extending the public comment period on its ...

Texas has pledged public money to research ibogaine, hoping for FDA approval to aid veterans with PTSD and addiction.

As mothers of children with this disease, we have wept helplessly in recent months as friends — fellow members of a club we ...

Tayler said the FDA’s own research has highlighted that fact. “In the last National Youth Tobacco Survey, they asked youths if they used mint or menthol flavored and nearly 60% of them did,” she said.

The FDA issued a complete response letter to Genentech indicating it cannot approve the company’s biologic license ...

Unlike expensive positron emission tomography (PET) scans or invasive lumbar punctures, the new blood test measures the ratio of two proteins, pTau217 and ß-Amyloid 1-42, which are implicated in ...

The panel voted 10-1 to say the available data does not establish the efficacy of the drug, brexpiprazole, in combination ...

A California couple that had 21 children via surrogacy has been charged with felony child endangerment and neglect.

In a significant reversal and a major boost for the embattled vaping company, the U.S. Food and Drug Administration (FDA) on ...