The U.S. Food and Drug Administration has approved AbbVie's drug to treat adults with a type of lung cancer who have received ...

Gain exclusive insights into Nyxoah's Q1 2025 earnings highlights, FDA progress, and U.S. launch strategy for their Genio system.

Merck (MRK) stock in focus as the FDA approves its anticancer agent Welireg for two rare neuroendocrine tumors, expanding its ...

Peter Gillooly, CEO of The Wellness Company, made a formal complaint to HHS' Office of the Special Counsel and other agencies ...

Reuters, the news and media division of Thomson Reuters, is the world’s largest multimedia news provider, reaching billions ...

The FDA reinstated the employees who run the proficiency testing program. After this story was published, Vianca N. Rodriguez ...

This stark regulatory rejection, which contradicted Aldeyra’s repeated assurances of imminent approval ... the FDA’s CRL. Aldeyra revealed that: “the FDA stated in the letter that the ...

today announced the U.S. Food and Drug Administration (FDA) has approved RINVOQ ® (upadacitinib), 15 mg, once daily, for the treatment of adults with giant cell arteritis (GCA). 1 This comes ...

Novavax said Monday that the Food and Drug Administration was asking the company to run a new clinical trial of its vaccine after the agency grants full approval. The company said it had responded ...

“The agreement with the FDA on proteinuria as an appropriate primary endpoint for full marketing approval for DMX-200 in our phase 3 trial is an exceptional outcome, particularly given that DMX ...