FDA approves eflornithine for adult and paediatric patients with high-risk neuroblastoma

FDA

13 December 2023 - Today, the FDA approved eflornithine (Iwilfin) to reduce the risk of relapse in adult and paediatric patients with high risk neuroblastoma who have demonstrated at least a partial response to prior multi-agent, multimodality therapy including anti-GD2 immunotherapy.

This represents the first FDA approval of a therapy intended to reduce the risk of relapse in paediatric patients with high risk neuroblastoma.

Read FDA News

Michael Wonder

Posted by:

Michael Wonder

Posted in:

Cancer , Outcome , Medicine , US