Over the past 14 years, the two sites in Wyoming have collected more than 8,000 pounds of drugs. (April 26, 2025) ...

Officers in Flint and around the country partnered with the U.S. Drug Enforcement Administration on Saturday for national ...

The U.S. Food and Drug Administration announced earlier this month that it will be phasing out animal testing for some new ...

Over my forty years or so in and around dealing rooms and financial markets, I have heard many theories as to how to approach that problem and have settled on a process that has worked for me.

SDA4Drug is a semi-supervised, few-shot transfer learning method that improves single-cell drug response predictions by transferring knowledge from bulk-level data. It accurately identifies drug ...

Xia’s company—named Akeso, after a Greek goddess of healing—licensed the drug to U.S.-based Summit Therapeutics, which is testing it in the U.S. and will sell it there and in several other ...

BOSTON - The U.S. Food and Drug Administration (FDA) has awarded Fast Track designation to Verve Therapeutics' (NASDAQ:VERV) VERVE-102, a gene-editing treatment aimed at patients with hyperlipidemia ...

Drug major Cipla on Friday said it has received approval from the US health regulator to market a generic cancer treatment drug. The company has received the final approval from the US Food and ...

The drug, called BP16, is a biosimilar of an existing medicine called denosumab. The company tested the drug on 204 healthy volunteers. It compared the results with Prolia, being the original ...

Image: Professor Nicholas Turner wants urgent genetic testing of patients with advanced breast cancers to see if they could benefit The new drug is suitable for patients' tumours with mutations or ...

BOSTON - The U.S. Food and Drug Administration (FDA ... and a high lifetime risk of cardiovascular disease. The biotech company, currently valued at $271 million, has seen its stock trading ...