An investigation concluded that Biogen and the Food and Drug Administration ignored internal concerns from the company and skirted the agency's own written guidance to allow the Alzheimer's treatment Aduhelm to receive accelerated approval and hit the market at a cost to patients of $56,000 a year. The "unusual" collaboration unfolded through at least 115 meetings, calls and email exchanges between the company and the FDA in a year, said the report released Thursday by the Committees on Oversight and Reform, and Energy and Commerce. |
No comments:
Post a Comment