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Our Approach

Targeting Synaptic Dysfunction to Treat Neurodegenerative Disease

CervoMed is pursuing a new mechanism that is based on our understanding of how stress to the neuron, including inflammation, amyloid plaques, tau pathology or alpha synuclein deposits (i.e., Lewy bodies), drives the neurodegenerative process.

Scientific evidence has shown that the enzyme p38 alpha is a driver of neurological disease progression. Chronic activation of p38 alpha in the brain interferes with how neurons signal to one another – this is called synaptic dysfunction. Synaptic dysfunction leads to memory loss, executive function defects, deficits in motor function and other cognitive deficits, and if left untreated will result in neuron death over time.

We are developing an oral therapy, neflamapimod, that inhibits the enzyme p38 alpha. We believe that if neflamapimod is given in the early stages of neurological disease, it may reverse synaptic dysfunction, improve neuron health, and slow or prevent disease progression. CervoMed is investigating neflamapimod in our Phase 2b RewinD-LB clinical trial in patients with dementia with Lewy bodies.

CervoMed

Medicines for the Brain

Scientific data for neflamapimod has been published in certain medical journals and presented to the medical and scientific community at various medical meetings. Click below to access the data presentations.

Presentations and Publications

“The data from the trial of neflamapimod in DLB are very encouraging, setting the stage for more extensive testing. There are no approved treatments for DLB, the second most common cause of neurodegenerative dementia, and there is an urgent need to find therapies for this severe and progressive disorder.”

Jeffrey L. Cummings, MD, ScD, Joy Chambers-Grundy Professor of Brain Science and Director of the Chambers-Grundy Center for Transformative Science, UNLV School of Integrated Health Sciences