Fast Track designation awarded by the FDA serves as an external validation of the potential of NOX-A12 for unmet need in glioblastoma and could support an accelerated pathway to US regulatory approval
Fast Track designation for NOX-A12 follows recently announced FDA clearance of Investigational New Drug application for Phase 2 study in glioblastoma
Capitalizing on unprecedented NOX-A12 median Overall Survival of 19.9 months in chemotherapy resistant patients with residual tumor after surgery, TME Pharma actively pursues multiple sources of financing for NOX-A12 further clinical development, with a focus on non-dilutive financing
Fast Track designation is an important step in materializing discussions with potential wgdpvmlkcw rrs ueqxoksna gdxvhckj
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