Steven Lemery named acting associate director of Tissue Agnostic Drug Development at FDA’s OCE

Share on facebook
Share on twitter
Share on linkedin
Share on email
Share on print

Steven Lemery was named acting associate director of Tissue Agnostic Drug Development within FDA’s Oncology Center of Excellence.

Lemery will continue as division director for the Division of Oncology 3.

Lemery joined FDA in 2006 as a clinical reviewer in the Division of Biological Oncology Products, which ultimately re-organized into the Division of Oncology Products 2. He served as team lead on the Gastrointestinal Malignancies team in the Division of Oncology Products 2 where he supervised the review of multiple original and supplemental applications.

Subsequently, he assumed the role of the supervisory associate division director in DOP2, primarily leading activities for the melanoma/sarcoma and pediatrics/rare malignancies teams.

More recently, he has assumed the role of acting director of DO3 and is a member of the Medical Policy and Program Review Council. In various roles, he has contributed to Office- and OCE-led regulatory or policy initiatives. These have included both biosimilar development and tissue agnostic development.

In his new role in the OCE, Lemery will focus on scientific and policy efforts related to tissue agnostic drug development and lead outreach and education in this topic.

Table of Contents

YOU MAY BE INTERESTED IN

On Feb. 19, GRAIL Inc. announced that its pivotal NHS-Galleri trial failed to meet its primary endpoint of reduction in advanced stage cancers. The media and the market reacted as one would expect: GRAIL’s stock price halved the day after the announcement and at least three law firms said that they are conducting investigations in preparation for filing investor suits.
If you listen to GRAIL executives discuss the results of the long-awaited trial of the company’s multicancer detection test, you might be led to conclude that the company’s pivotal NHS-Galleri study had an overwhelmingly positive result.
Undeterred by the negative topline result of its pivotal trial of Galleri, a multicancer detection test, the test’s sponsor, GRAIL, said it’s forging ahead with its plan to get FDA approval and reimbursement from CMS and private insurers.
Philip E. Castle, director of the NCI Division of Cancer Prevention, said he was disappointed to hear that GRAIL’s NHS-Galleri trial did not meet its primary endpoint of reduction in late-stage cancers.

Never miss an issue!

Get alerts for our award-winning coverage in your inbox.

Login