This webinar is a livestream of the Institute’s pre-ESMO symposium in Madrid and is a non-commercial event open to the public at no cost. Attendance at ESMO is not required. This discussion is designed for a broad oncology audience and will provide relevant insights for patients, clinicians, healthcare providers, non-profits, health economists, and professionals across the pharmaceutical and life sciences sectors.
Phase I oncology trials are evolving rapidly, driven by advances in precision medicine, immunotherapy, and cell and gene therapies. At the same time, China is emerging as a major hub for early oncology development, reshaping global research and regulatory strategies.
This multi-stakeholder symposium will examine how Phase I trials can generate stronger evidence, improve decision-making, and deliver greater value across the oncology development continuum. Topics include:- The evolving role of Phase I trials: Beyond safety to dose optimization, biomarker-driven development, and early efficacy signals.
- Global shifts in oncology innovation: The impact of China’s growing role and increasingly global development strategies.
- Execution under increasing complexity: Balancing speed, scientific advancement, operational demands, and patient value.
EVP, Head of Clinical Development and Chief Medical Officer, Immunocore
Director, Clinical Research START Madrid-FJD
Chief Scientific Officer / CEO / Director of Clinical Research / Virginia Cancer Specialist Co-director of Clinical Research, NEXT Oncology
Head of Clinical Programs and Study Operations, Early Oncology, AstraZeneca
Research and Patient Engagement Director Cancer Patients Europe
Chief Medical Officer Jiangsu Hansoh Pharmaceutical Group Co., Ltd.
Solid Tumor Head & Senior Medical Director, IQVIA Oncology Center of Excellence
Executive Director, IQVIA Institute for Human Data Science
