Experimental drug zervimesine made available to patients with lewy body dementia
NCT ID NCT06961760
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This expanded access program offers the experimental drug zervimesine (CT1812) to people aged 50 to 86 with mild-to-moderate dementia with Lewy bodies. Participants take one 100 mg pill daily for up to a year. The goal is to provide access to the drug and collect long-term safety information.
What this could mean
Our plain-language read of the trial. This is informational only — not medical advice or a prediction.
- Active substance
- zervimesine (CT1812)
- What this could lead to
- If this program shows that zervimesine is safe and well-tolerated over a year, it could support further research into a treatment for dementia with Lewy bodies.
- What could go wrong
- This is an expanded access program, not a formal trial, so it provides limited evidence of effectiveness. The drug is still experimental, and long-term risks are not fully known.
This is an AI summary of the original study and may miss details. Read our disclaimer.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Banner Sun Health Research Institute
Sun City, Arizona, 85351, United States
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Columbia University Medical Center
New York, New York, 10032, United States
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Mayo Clinic - Rochester
Rochester, Minnesota, 55905, United States
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Ohio State University Wexner Medical Center (OSUWMC)
Columbus, Ohio, 43210, United States
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Stanford Neuroscience Heath Center
Palo Alto, California, 94304, United States
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Summit Headlands LLC
Portland, Oregon, 97210, United States
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University of Colorado Denver - Anschutz Medical Campus
Aurora, Colorado, 80045, United States
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University of Miami - Department of Neurology
Boca Raton, Florida, 33433, United States
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