Focus oncology development on the patient, manage trial complexity, and increase predictability and speed.
Combination therapies are reshaping the future of oncology, but optimizing their dosing remains one of the field’s most complex challenges. This panel discussion explores how biotech and pharma teams can move beyond the traditional maximum tolerated dose (MTD) paradigm to embrace innovative, model-informed strategies that align with FDA’s Project Optimus.
Attendees will gain insights into designing effective combination trials, leveraging biomarkers and pharmacologic data and applying simulation tools to streamline the development process. Whether planning a first-in-human study or expanding a global trial, this session will equip attendees with the knowledge to navigate regulatory expectations and deliver better outcomes for patients.
Register now to explore how innovative trials are shaping the future of clinical research and enhancing patient outcomes.
Jeff Hodge, MS, Vice President Early Phase Oncology, Hematology-Oncology Center of Excellence, IQVIA
Michael Brave, Vice President, Therapeutic Strategy, IQVIA
Howard “Skip” Burris, MD, President, Sarah Cannon Research Institute
Zheng Liu, Director of Quantitative Clinical Pharmacology, IQVIA
For more information and to register, click here.
Focus oncology development on the patient, manage trial complexity, and increase predictability and speed.
Specialized expertise and customized solutions across 14 therapeutic centers of excellence, including oncology, GI/NASH, pediatrics, neurology and rare diseases.