Clinical DataCervoMed's latest data from the open label extension (OLE) study is boosting investor confidence, and a more risk-on approach is seen heading into the next steps for neflamapimod in dementia with Lewy bodies (DLB) patients.
Product ImprovementNewly manufactured capsules of neflamapimod have meaningfully improved CDR-SB scores compared to old capsules in the initial 16 weeks, indicating significant cognitive benefits.
Regulatory ProspectsManagement has indicated a potential meeting with the FDA after complete OLE 32 week data and data from the French study at a higher dose, which may allow CervoMed to proceed directly to a Phase 3 trial.