Jean-Yves Douillard appointed chief medical officer of ESMO

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

JEAN-YVES DOUILLARD was appointed the first chief medical officer of the European Society for Medical Oncology. A senior staff position based at the Society’s headquarters in Lugano, Switzerland for a fixed two-year term, the CMO will lead the development of ESMO’s scientific strategy and activities.

Douillard’s appointment follows a six-month selection process open to all ESMO members with the necessary high-level qualifications and experience for the role. Candidates were also required to have held senior ESMO leadership positions.

In a career spanning more than 30 years, Douillard has achieved international recognition as a leading expert in lung cancer and gastrointestinal oncology, holding a number of leadership positions.

At the University of Nantes, he was professor in medical oncology, while at the Integrated Centers of Oncology Rene Gauducheau, also in Nantes, he was head of the Medical Oncology Department and later director of clinical and translational research. In addition, he spent a total of four years working in the U.S., initially at the NCI and later at the FDA Center for Drug Evaluation and Research.

Douillard has led clinical trials in relation to lung cancer and GI tumors and investigated targeted therapies, publishing his work in leading scientific journals. He has also served as chair of the ESMO Educational Committee and as a member of the society’s executive board.

YOU MAY BE INTERESTED IN

Recently, HHS Secretary Robert F. Kennedy Jr. posted a video montage featuring himself shirtless in jeans, working out with Kid Rock. The duo is in a blue-lit grotto with a cold plunge and sauna. Set to Kid Rock’s “Bawitdaba” and intercut with a selection of patriotic imagery, the video ends with the two men in a hot tub, chugging what appears to be milk.
In January, FDA released a draft guidance entitled “Minimal Residual Disease and Complete Response in Multiple Myeloma: Use as Endpoints to Support Accelerated Approval.” This release came roughly 20 months after the Oncologic Drugs Advisory Committee (ODAC) voted unanimously that minimal residual disease (MRD) negativity, in combination with complete response (CR), is an acceptable primary endpoint to support accelerated approval for multiple myeloma (MM) therapies. 

Never miss an issue!

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

Login