Session Goals
Currently, there is no doubt that biologic drugs stand for a real revolution in the global therapeutic market. According to the most recent data from the Antibody Society, there are 113 mAbs already approved by the FDA, 22 in review, and close to 600 in clinical trials. With more than 70% biologics in the top ten pharma drugs by sales and a global therapeutic monoclonal antibody market revenue forecast of $300 billion by 2025, the discovery of new biologic drugs, and especially new antibody formats, is the highest priority in major pharma and biotech companies. One of the main drivers of these trends imply the evolution from conventional naked whole length antibodies to the engineering of new antibody fragments, formats, conjugates, bi- and multispecifics, CAR-T cells, etc., and new biologic production processes.
The session will address and review some of the front-edge technologies and approaches that are being currently used by the industry, academia, and at the clinical level, with leading experts in this exciting therapeutic area.