Norgine submits marketing authorisation application to the EMA for eflornithine (difluoromethylornithine) in high risk neuroblastoma

Norgine

6 January 2025 - Norgine today announced that it completed its marketing authorisation application filing to the EMA for eflornithine in high-risk neuroblastoma. 

This follows the submissions in April 2024, via Project Orbis, in Australia, Switzerland and the United Kingdom.

Read Norgine press release

Michael Wonder

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Michael Wonder

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Medicine , Europe , Paediatrics , Dossier