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

  • Banner Sun Health Research Institute

    Sun City, Arizona, 85351, United States

  • Columbia University Medical Center

    New York, New York, 10032, United States

  • Mayo Clinic - Rochester

    Rochester, Minnesota, 55905, United States

  • Ohio State University Wexner Medical Center (OSUWMC)

    Columbus, Ohio, 43210, United States

  • Stanford Neuroscience Heath Center

    Palo Alto, California, 94304, United States

  • Summit Headlands LLC

    Portland, Oregon, 97210, United States

  • University of Colorado Denver - Anschutz Medical Campus

    Aurora, Colorado, 80045, United States

  • University of Miami - Department of Neurology

    Boca Raton, Florida, 33433, United States

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