Ark receives approval EMEA for Cerepro
London, UK-based group Ark Therapeutics has received approval from the European Medicines Agency (EMEA) for Cerepro, its high-grade glioma treatment for pediatric patients.
The EMEA has approved the development of Cerepro for children from one month to 18 years of age with operable high-grade glioma. The treatment will be used to prevent tumors from recurring once they have been removed.
As from July 26, 2008, the European Pediatric Use Regulation requires the EMEA to ensure all new products have a suitable pediatric development plan.
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