Vivek Subbiah posted on LinkedIn

“Excited to announce my latest venture!

Hosting an interview with Dr. Tobias Janowitz & Karen Winkfield authors of ‘Analysis & Optimization of Equitable US Cancer Clinical Trial Center Access by Travel Time’ published in JAMA Oncology.

Tune in to the podcast for insights into equitable access to cancer clinical trials

Link.”

Source: Vivek Subbiah/LinkedIn

Vivek Subbiah is the Chief of Early-Phase Drug Development at the Sarah Cannon Research Institute (USA). He is the former Executive Director of Oncology Research at the MD Anderson Cancer Network and a former Associate Professor in the Department of Investigational Cancer Therapeutics at The University of Texas MD Anderson Cancer Center. Dr. Vivek Subbiah has served as the principal investigator in over 100 phase I/II trials and co-investigator in over 200 clinical trials and is known for his leadership in several first-in-human and practice-changing studies that directly led to approvals from the FDA, European Medicines Agency, and other agencies across the world. He is an expert in tumor agnostic precision oncology and leads the BRAF and RET tissue agnostic studies to FDA approval.