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Day One takes on Novartis with FDA nod for Ojemda in broader common childhood brain tumor use

Day One takes on Novartis with FDA nod for Ojemda in broader common childhood brain tumor use
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Day One s OJEMDA™ (tovorafenib) Receives US FDA Accelerated

Day One s OJEMDA™ (tovorafenib) Receives US FDA Accelerated Approval for Relapsed or Refractory BRAF-altered Pediatric Low-Grade Glioma (pLGG), the Most Common Form of Childhood Brain Tumor

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