Mid-size French drugmaker Ipsen (Euronext: IPN) and California’s Day One Biopharmaceuticals (Nasdaq: DAWN) have announced a global partnership, outside the USA, for tovorafenib.
Ipsen has secured rights in these countries for the oral, once-weekly, type II RAF inhibitor for pediatric low grade glioma (pLGG), the most common form of childhood brain cancer, i and any future indications developed by Day One.
Tovorafenib was granted Orphan Drug Designation and received US Food and Drug Administration (FDA) approval in April 2024 as a monotherapy treatment for patients six months and older with relapsed or refractory pLGG harboring a BRAF fusion or rearrangement, or BRAF V600 mutation. It is marketed as Ojemda in the USA.
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