On May 12, 2022, the Pediatric Oncology Subcommittee of the Oncologic Drug Advisory Committee (ODAC) consider and discuss the potential utility and steps to validation of an intermediate clinical endpoint, response to induction therapy, in the development of new drugs for the first-line treatment of patients with high-risk neuroblastoma.

The European Medicines Agency (EMA) has also been invited to present on both days.