New hope for Alzheimer's psychosis: Long-Term drug trial underway
NCT ID NCT07459660
First seen Jun 25, 2026 · Last updated Aug 07, 2026 · Updated 4 times
Summary
This study is testing the long-term safety of a drug called ML007C-MA for people with Alzheimer's disease who also have hallucinations and delusions. About 210 adults who completed a previous study will take the drug twice daily for up to 52 weeks. The goal is to see if the drug remains safe and tolerable over time.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- ML007C-MA (a combination drug taken twice daily)
- What this could lead to
- If it works, this could provide a safe, long-term option to ease hallucinations and delusions in people with Alzheimer's disease.
- What could go wrong
- This is an early-phase, open-label study with no placebo group, so results may not confirm effectiveness. Side effects or lack of benefit could still occur.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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About 210 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Mar 2026
- Expected to finish
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Mar 2029
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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55 to 91 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria 1. Willing and able to provide written informed consent, or, if deemed lacking in the capacity to provide informed consent, the following requirements for consent must be met: 1. The participant's LAR must provide written informed consent. AND 2. The participant will provide informed assent. 2. Has completed the Double-Blind Treatment Period of an antecedent study with ML-007C-MA (ie, ML-007C-MA-221). 3. May benefit from long-term therapy with open-label ML-007C-MA treatment, in the judgment of the investigator. 4. Has a designated study care partner who is in contact with the participant frequently enough to accurately report on the participant's symptoms and adherence to study drug. 5. Resides in a stable living environment (eg, home, residential assisted living, or nursing home facility) and is expected to remain in the living situation throughout the study. Exclusion Criteria 1. Under the care of hospice, bed-bound, or receiving end-of-life palliative care. 2. Requires treatment with protocol-defined prohibited medications. 3. Has developed a new or worsening medical comorbidity during or since the antecedent study that, in the opinion of the investigator and/or medical monitor, would compromise participant safety, interfere with the participant's ability to comply with study procedures, would preclude obtaining voluntary consent/assent, and/or would substantially impair the evaluation of study assessments. 4. Has or had a clinically significant abnormal physical examination, vital sign, ECG or clinical laboratory safety result during or since the antecedent study that would compromise participant safety, interfere with the participant's ability to comply with study procedures, and/or would confound the interpretation of the outcome measures in the study in the opinion of the investigator. 5. Has developed an allergy or other intolerance to ML-007C-MA, its active ingredients or their excipients since the antecedent study. 6. Has an elevated risk of suicidal behavior.
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
8 sites in 3 countries. The list below names each one and where it is.
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The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Clinical Site
Anaheim, California, 92805, United States
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Clinical Site
Doral, Florida, 33122, United States
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Clinical Site
Miami, Florida, 33155, United States
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Clinical Site
Miami, Florida, 33173, United States
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Clinical Site
Miami Gardens, Florida, 33014, United States
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Clinical Site
Orlando, Florida, 32807, United States
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Clinical Site
Pernik, Pernik, 2304, Bulgaria
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Clinical Site
Toulouse, 31059, France
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