The failure of CervoMed’s much-anticipated RewinD-LB Phase IIb study of neflamapimodin in patients with dementia with Lewy bodies (DLB) has left investors disappointed and the company scratching its head.
Topline data show the product, CervoMed’s lead candidate, missed the primary endpoint of change in the clinical dementia rating sum of boxes and all of the trial’s key secondary goals.
Key Takeaways
CervoMed's lead product has unexpectedly failed in a Phase IIb study in Lewy body dementia.
The reasons for the failure are not clear,...
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