CervoMed reports initial biomarker data from Phase 2a neflamapimod trial
Results show reduced neurofilament light levels over 12 weeks in nfvPPA patients at the ISFTD meeting. Further data is expected later this year.
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Clinical-stage biotechnology company developing treatments for age-related brain disorders
cervomed.comLast updated
In short: CervoMed reported nfvPPA biomarker data and advanced neflamapimod toward Phase 3 for DLB.
Results show reduced neurofilament light levels over 12 weeks in nfvPPA patients at the ISFTD meeting. Further data is expected later this year.
The company introduces a 50 mg oral tablet for neflamapimod, securing FDA removal of exposure limits to enable a twice-daily dosing regimen.
The twelve-week biomarker findings will be presented at the ISFTD Annual Meeting in October to support ongoing neurodegenerative disease development.
The company is prioritizing a strategic partnership to advance neflamapimod into Phase 3 for DLB, and presented new analyses at AAIC 2026.
On October 12, 2026, CervoMed reported initial 12-week biomarker data from the open-label portion of its Phase 2a trial of neflamapimod in nonfluent variant primary...
Prioritizing strategic partnership to advance neflamapimod into Phase 3 for the treatment of dementia with Lewy bodies (DLB) ...
CervoMed Inc. (NASDAQ:CRVO) earns a place on our top 10 stocks under $5 that could triple. On March...
FDA feedback enables CervoMed to proceed with proposed endpoints, patient enrichment strategy, and other key aspects of Phase 3 trial design to support potential New...
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