Zervimesine: A Long-Needed Approach to Addressing DLB
Preclinical and early clinical studies of zervimesine (CT1812), our investigational, small-molecule oral therapy, have demonstrated its ability to block harmful α-synuclein oligomers from binding to neurons, which may slow or prevent DLB progression.
Only a few symptomatic treatments (to control agitation) for dementia with Lewy bodies are approved today, and at present, no disease-modifying therapeutics exist for these patients. Cognition Therapeutics conducted the Phase 2 SHIMMER study to investigate whether zervimesine has a beneficial effect in adults diagnosed with mild to moderate DLB. The study was supported by a grant awarded by the National Institute of Aging (part of the National Institutes of Health).
SYMPTOMS OF DLB
- Fluctuating alertness and attention levels
- Psychosis and behavioral symptoms:
- Vivid visual and auditory hallucinations
- Delusions
- Agitation and anxiety
- Motor symptoms resembling Parkinson’s disease:
- Resting tremors
- Muscle stiffness
- Shuffling gait
- REM sleep disorder (acting out dreams while sleeping)
Understanding DLB Psychosis
Approximately 80% of people with DLB experience some combination of neuropsychiatric symptoms, which can vary in presentation and severity but include delusions, hallucinations, agitation, aggression and depression.
The early onset of psychosis symptoms is a critical factor that helps distinguish DLB from other dementias, particularly Alzheimer’s disease.
The unpredictability and complexity of these symptoms place a considerable burden on patients and caregivers. They don’t just disrupt everyday life; they also lead to considerable emotional strain, as well as earlier institutionalization for patients, leading to increased healthcare needs and costs.
Antipsychotic medications that are used in other diseases are not approved for the treatment of DLB, due to the high risk of severe, and sometimes fatal, adverse reactions including severe parkinsonism, sedation, and immobility.
Our Commitment to the DLB Community
Phase 2 SHIMMER study:
- Complete with results: 130 adults with mild-to-moderate dementia with Lewy bodies (DLB) were randomized to receive one of two doses of zervimesine or placebo for six months.
- Supported by a $30 million grant from the National Institute on Aging (NIA) of the National Institutes of Health (NIH).
- On December 18, 2024, a webcast was held to review topline results from the SHIMMER study. Click here for the archive.
- For more information, please visit clinicaltrials.gov and reference study ID NCT05225415.
