The advent of the age of immuno-oncology has led to a dramatic shift in our conception of how to treat cancer patients. The approval of six checkpoint inhibitors in the United States has transformed clinical management and patient outcomes in some tumor types, but in other indications the clinical benefit has been more modest or even negligible.
With the two leading checkpoint inhibitors (Merck’s Keytruda and BMS’ Opdivo) leading the way here, with some 1,400 combination trials ongoing, a diverse array of approaches, targets, and modalities are being combined with checkpoint inhibitors.
The need to increase patient responsiveness to treatment and extend duration of remissions across all cancers has resulted in an intensive clinical development push around combinations, generating debate about which types of tumors make better targets for these therapies and what point in a patient’s course of treatment is the optimal time to administer them.
This webinar, with esteemed colleagues from Merck, MD Anderson, f-star, eFFECTOR, and Cancer Research Institute, is intended to be a lively discussion of the pros and cons, challenges, and opportunities that these various clinical development strategies entail.
Vanessa M. Lucey, Ph.D., MBA, director of CRI Clinical Accelerator and Venture Fund, discusses the immuno-onocology landscape in this webinar for the biotechnology industry.
This webinar is organized by Cello Health BioConsulting.
Vanessa M. Lucey, Ph.D., MBA, director of CRI Clinical Accelerator and Venture Fund, will also speak on a panel at Cancer Progress on May 6, 2020, at Convene in New York City. Cancer Progress is organized by Cello Health BioConsulting.
Photo by Andras Vas on Unsplash