Could fat stem cells fight Alzheimer's? new trial tests repeat brain injections
NCT ID NCT07373067
First seen Jun 26, 2026 · Last updated Aug 27, 2026 · Updated 3 times
Summary
This early-stage trial tests whether repeated injections of a patient's own fat-derived stem cells into the brain are safe for people with mild to moderate Alzheimer's. Nine participants who previously received a single dose will now get up to six injections every two months. Researchers will monitor side effects and check for changes in brain proteins linked to Alzheimer's.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- autologous adipose-derived stem cells (RB-ADSC)
- What this could lead to
- If safe and effective, this approach could slow Alzheimer's progression by reducing harmful tau proteins in the brain.
- What could go wrong
- This is a very early, small trial (9 people) focused on safety, not proof of benefit. Stem cell injections into the brain carry risks like infection or inflammation.
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 1
The first testing in people. Mainly checks safety and dose, usually in a small group.
- Participants
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About 9 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Sep 2028
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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45 years and older
- 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Successful completion of the Phase 1 single dose administration study of RB-ADSC, Protocol RB-ADSC-02. 2. Written informed consent to participate in this Phase 1b Extension Study either provided by the participant or a legal representative 3. The participant must have a relative/caregiver who is alert for possible side effects. 4. The caregiver must separately meet the specified inclusion/exclusion criteria for caregivers for this Phase 1b Extension Study. Exclusion Criteria: 1. Participant experienced treatment related SAE or DLT in Protocol RB-ADSC-02 2. Participants who, in the opinion of the Investigator, are unsuitable for this Phase 1 Extension Study
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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 official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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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.
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