Re-Thinking Clinical Trials in Oncology
 Assessing the landscape of novel trial design for cancer therapies to improve data collection, enhance patient access, and drive clinical outcomes for breakthrough therapies

October 28, 2020 | Live Virtual Forum (EST)

Marcel Rozencweig

CMO NeoTX Therapeutics

Dr. Rozencweig is a medical oncologist with more than 40 years of experience in clinical trials and anti-cancer drug development at the National Cancer Institute and in the pharmaceutical industry. Dr. Rozencweig has served in various global drug development leadership positions at Bristol-Myers Squibb in worldwide clinical R&D, strategic marketing, portfolio management, and portfolio development. He built and led the BMS clinical research group that developed all NCE’s brought to market in the field of cancer from 1983 to 2001. Dr. Rozencweig has held senior management positions at several small US and international biotechnology companies.

WEDNESDAY, OCTOBER 28

11:15 AM Early Development & Regulatory Strategy in Oncology :What’s Important to Get New Products Approved?

What do you need to think about early in development to get new products approve? In a very condensed time frame for oncology products, understand why you need think “end game” early on.