Director of NCI Nominated as New FDA Commissioner

Publication
Article
Oncology NEWS InternationalOncology NEWS International Vol 15 No 4
Volume 15
Issue 4

President Bush has nominated NCI director Andrew C. von Eschenbach, MD, as commissioner of the Food and Drug Administration (FDA).

WASHINGTON—President Bush has nominated NCI director Andrew C. von Eschenbach, MD, as commissioner of the Food and Drug Administration (FDA). Dr. von Eschenbach has served as acting FDA commissioner since the resignation of Lester M. Crawford, DVM, PhD, in September 2005. Mike Leavitt, secretary of Health and Human Services, called his nomination an "inspired" choice. "His career has been defined by his vision for progress in research and passion for the care of patients—two qualities which will serve the agency and the American public well," he said.

Plan B Controversy

If confirmed by the Senate, Dr. von Eschenbach will become the third FDA commissioner under President Bush. His confirmation immediately became embroiled in a political fight. Sen. Hillary Rodham Clinton (D-NY) and Sen. Patty Murray (D-Wash) announced that they would put a hold on Dr. von Eschenbach's nomination, a Senate procedure that would prevent his confirmation, "until the FDA issues a decision on Plan B, yes or no." Plan B is the controversial "morning after pill." An FDA advisory board and FDA medical reviewers have recommended approving the drug for over-the-counter sale, which social and religious conservatives oppose because they contend it could cause early abortions and encourage promiscuity.

Dr. von Eschenbach joined NCI in January 2002 after a distinguished career as a urologic surgeon and cancer advocate at the M.D. Anderson Cancer Center. Since his appointment as acting FDA commissioner, the day-to-day management of NCI has been overseen by chief operating officer John Niederhuber, MD, an arrangement that will continue until Dr. von Eschenbach is confirmed as FDA commissioner.

Recent Videos
Being able to treat patients with cevostamab who have multiple myeloma after 1 to 3 prior lines of therapy vs 4 lines may allow for better outcomes.
Using the monitoring of symptoms and quality of life platform may provide a quick and efficient system for patients to submit outcome data.
2 experts are featured in this series.
With many treatments emerging in the EGFR-mutated lung cancer landscape, sequencing therapy has emerged as a key consideration for these patients.
Although a greater risk of CNS relapse may emerge with immunotherapy-based backbones, toxicities associated with chemotherapy are avoided.
Current FDA expectations may allow patients to return to their community physicians at 2 weeks after administration of anitocabtagene autoleucel.
Based on its mechanism of action, anito-cel may cause fewer instances of cytokine release syndrome and delayed toxicities vs other therapies.
2 experts are featured in this series.
Related Content