Interactive workshop with participants from academia, industry, and the regulators exploring the opportunities and challenges in tumour agnostic cancer drug development.
Sessions will discuss the successes and failures of previous trials in this area, explore trial design, and discuss biomarker development for patient stratification.
- To understand the current landscape of tumour agnostic drug development
- To be able to discuss suitable trial designs to deliver such studies
- To develop an understanding of biomarker development and the need for agnostic tumour registrations
- To understand the regulatory environment around these registrations
The target is a multidisciplinary audience of academia representatives, EU and US regulatory bodies (EMA, FDA, National Agencies), the pharmaceutical industry, HTAs, and patient advocates.