George Tidmarsh, who leads the FDA’s powerful drugs office known as CDER, has been placed on leave from the agency, according to reports.
According to the New York Times, Tidmarsh had raised concerns about a …
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.
															George Tidmarsh, who leads the FDA’s powerful drugs office known as CDER, has been placed on leave from the agency, according to reports.
According to the New York Times, Tidmarsh had raised concerns about a …