Allogeneic Stem Cells for Mild to Moderate Alzheimer's
Allogeneic Adipose Tissue Derived-stem Cells in Alzheimer Disease
Recruiting
Phase 1Phase 2Interventional Study
Alzheimer Disease
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Prior Safety Data
This treatment has already been tested in at least one earlier human trial.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
50 – 85
Sex
Any
Trial phase
Phase 1/2
Study type
Interventional
Purpose
Treatment
Participants needed
9 (estimated)
Sponsor
University Hospital, Toulouse · Other
Who this trial is looking for
This trial is looking for patients aged 50 to 85 with mild to moderate Alzheimer's disease. Participants will receive stem cells through an IV to see if it is safe.
Are You a Good Fit for This Trial?
You may be able to join if
I am between 50 and 85 years old
I have a diagnosis of Alzheimer's disease
I have a MMSE score between 14 and 26
I have a CDR score of 1 or more
I can have PET or MRI scans
I have consent from my caregiver
I have social security coverage
You may not be able to join if
I have another brain disease that causes dementia
I have had cancer diagnosed in the last 5 years
I have metal fragments in my eyes or brain
I use corticosteroids regularly
I am pregnant or breastfeeding
I have an autoimmune disease except psoriasis
I am under guardianship or legal protection
I can't take a PET scan due to previous research
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer a few quick questions to see if you may meet the eligibility requirements.
A3D is a phase I/II clinical trial. The primary objective is to evaluate the safety of allogeneic adipose tissue derived-stem cells (AdMSC) administered by intravenous (IV) route in mild to moderate Alzheimer disease (AD) using a dose escalation protocol.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Patient between 50 and 85 years old
* AD diagnosis according to NIA-AA 2011 criteria at a mild to moderate stage :
MMSE score between 14 and 26 (include) positive AD amyloid biomarker
* CDR (clinical dementia rating) score ≥ 1
* Patient with no absolute contraindications for…
Inclusion Criteria:
* Patient between 50 and 85 years old
* AD diagnosis according to NIA-AA 2011 criteria at a mild to moderate stage :
MMSE score between 14 and 26 (include) positive AD amyloid biomarker
* CDR (clinical dementia rating) score ≥ 1
* Patient with no absolute contraindications for PET or MRI scans
* Consent signed by the patient and study partner
* presence of primary caregiver
* Patient with social security coverage
Exclusion Criteria:
* Brain disease (other than AD) that may cause dementia
* Presence of concomitant pathologies not permitting participation in the study
* Concurrent participation in other research that may influence the testing of the A3D study
* Carrier of a pacemaker, valve prosthesis or other internal magnetic or electronic system, history of neurosurgery or aneurysm surgery, presence of metal fragments in the eyes, brain or marrow, claustrophobia
* PET scan performed in the previous year (research context)
* History of cancer diagnosed within the last 5 years
* Presence of \> 4 brain microbleeds, a single area of superficial siderosis, or evidence of previous macrohaemorrhage assessed by brain MRI scan
* Regular use of corticosteroids or other steroidal anti-inflammatory drugs (e. g. prednisone)
* Presence of an autoimmune disease (e. g. rheumatoid arthritis, systemic lupus erythematosus) with the exception of psoriasis
* Pregnant or breastfeeding woman
* Adults under guardianship or other legal protection, deprived of their liberty by judicial or administrative decision For patients who will participate in the optional adipose puncture (only carried out in the Toulouse center): Antithrombotic treatment and xylocaine allergy are prohibited.
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