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Ojemda (tovorafenib) – New orphan drug approval

April 23, 2024 - The FDA announced the approval of Day One Pharmaceuticals’ Ojemda (tovorafenib), for the treatment of patients 6 months of age and older with relapsed or refractory pediatric low-grade glioma (pLGG) harboring a BRAF fusion or rearrangement, or BRAF V600 mutation.

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