For decades, the FDA has long been thought of as a steady hand of gold-standard regulatory work for the most innovative drugs in the world.
This year, the agency has looked more like a reality …
Sarepta Therapeutics’ long-awaited confirmatory study of two of its ‘exon-skipping’ therapies for forms of Duchenne muscular dystrophy failed to meet its primary endpoint, the company
One day after stepping down as CDER Director, George Tidmarsh has said he will fight the investigations into his conduct and is reconsidering his decision.
Two federal district courts have reached opposite conclusions in cases challenging states’ authority to regulate how drugmakers distribute 340B discounts. An Oklahoma federal judge on
uniQure has revealed that the FDA has said it is not prepared to review its Huntington’s gene therapy in what seems to be a change
Eli Lilly plans to build another facility to make its oral GLP-1 drug orforglipron. The $3 billion site will be located in Katwijk, the Netherlands.
															For decades, the FDA has long been thought of as a steady hand of gold-standard regulatory work for the most innovative drugs in the world.
This year, the agency has looked more like a reality …