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Sam Blackman: US FDA approved the first targeted medicine for the treatment of patients with relapsed or refractory pediatric low-grade glioma
Apr 28, 2024, 13:23

Sam Blackman: US FDA approved the first targeted medicine for the treatment of patients with relapsed or refractory pediatric low-grade glioma

Sam Blackman, Co-founder and Chief Medical Officer of Day One Biopharmaceuticals, shared a post by Day One Biopharmaceuticals, on X:

“Proud of the hard work from the Day One Biopharmaceuticals teams and the broader pediatric oncology community to make this achievement possible! We did it!”

Quoting Day One Biopharmaceuticals‘s post:

We are proud to share the accelerated approval by the US FDA of the first targeted medicine for the treatment of patients with relapsed or refractory pediatric low-grade glioma (pLGG) with a BRAF fusion or rearrangement, or BRAF V600 mutation.

Source: Sam Blackman/X and Day One Biopharmaceuticals/X