European Commission Approves VORANIGO® (vorasidenib) for Grade 2 IDH-Mutant Glioma
“Today’s EU approval of VORANIGO is a landmark moment for people in the EU living with IDH-mutated glioma who have been waiting more than two decades for new treatment options. VORANIGO is the first EMA-approved therapy specifically designed to target mutant IDH enzymes in Grade 2 glioma and represents a long-awaited shift in the treatment paradigm. As a leader in precision medicine, we’re grateful to the researchers, patients and advocates who have helped expand our understanding of IDH inhibition and bring this breakthrough to the EU,” said Islam Hassan, Global Head of Development-Neuro-Oncology & Senior Director, LS/LCM at Servier.
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