Clinical TrialsTPI-287 demonstrated an overall response rate of 60% in a Phase 1 trial for rGBM, with a 96% disease control rate, indicating promising efficacy.
Regulatory ProspectsThe totality of data could support a formal discussion with the FDA around a potential filing or accelerated approval pathway for Berubicin without another trial.
Strategic DevelopmentCNS Pharmaceuticals is upgrading shares to Buy due to the pivot to its oncology asset TPI-287, which is in development for recurrent glioblastoma (rGBM).