Positive FDA feedback on Hemerion’s clinical strategy for glioblastoma
The Food and Drug Administration (FDA) has issued a positive feedback on Hemerion’s clinical strategy following a Type C Meeting held in November 2025. The U.S. health authority confirmed the relevance of Hemerion’s proposed clinical and regulatory strategy for the Pentalafen® / Heliance® technology in the treatment of newly diagnosed glioblastoma patients in the United …