Leaders of two congressional committees probing the approval of Biogen Inc.’s new Alzheimer’s drug pressed the Food and Drug Administration for more information on “apparent anomalies” in the agency’s review of the $56,000-a-year therapy.
Leaders of two congressional committees probing the approval of Biogen Inc.’s new Alzheimer’s drug pressed the Food and Drug Administration for more information on “apparent anomalies” in the agency’s review of the $56,000-a-year therapy.
