Alzheimer's Disease Trial, Recruiting NCT05926011 Sponsor: REGEnLIFE SAS Condition: Alzheimer's Disease
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Alzheimer's Disease Trial, Recruiting

NCT05926011
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People aged between 55 and 85 years old (inclusive)
  • People who have been diagnosed with Alzheimer's disease (AD) according to a specific set of international medical guidelines from 2011
  • People with mild-to-moderate Alzheimer's disease, based on a standard memory and thinking test score between 10 and 26
  • People who have had relevant blood test results (covering thyroid, vitamins, liver, kidney, blood cells, and other markers) within the past year that are consistent with an Alzheimer's diagnosis, as assessed by the trial doctor
  • People who have had a brain CT scan or MRI scan within the past year that is consistent with an Alzheimer's diagnosis, as assessed by the trial doctor
  • People already taking Alzheimer's medications (such as memantine or acetylcholinesterase inhibitors) or certain mental health medications (such as anti-anxiety, antidepressant, or antipsychotic drugs), provided the dose has been stable for at least 4 weeks before joining
  • People who have a caregiver who is regularly present and able to support them throughout the trial, as assessed by the trial doctor
  • People who are enrolled in the French social security system
  • People who have provided signed and dated consent to take part, along with their caregiver

Who may not be able to join:

  • People who are under a French legal protection measure (such as "sauvegarde de justice", "tutelle", or "curatelle")
  • People who are detained or hospitalised without their consent
  • Women who have not yet gone through menopause
  • People currently taking a disease-modifying Alzheimer's treatment, such as Leqembi®, or any similar treatment that may become authorised in France before the trial ends
  • People who live in a medical or care facility
  • People who have had surgery on the stomach area or head within the 3 months before joining
  • People who have skin sores or wounds on the stomach area or head
  • People who have a serious, life-threatening illness (for example, active cancer, unstable heart failure, or severe liver, kidney, or breathing problems)
  • People who have had a stroke within the 3 months before joining
  • People who have metal objects (such as iron, nickel, cobalt, or metal alloys) on or near the head or stomach, or who have a pacemaker implanted
  • People who are at risk of having epileptic seizures
  • People who have a genetic form of Alzheimer's disease
  • People with significant physical or sensory difficulties that could interfere with neurological testing
  • People with chronic psychosis or a history of psychotic episodes
  • People with alcohol or drug addiction
  • People with known vitamin B12 or folic acid deficiencies that are not being treated with supplements
  • People with known hypothyroidism (underactive thyroid) that is not being treated
  • People who have taken part in another clinical trial involving an experimental drug or medical device within the 30 days before joining
  • People who the trial doctor determines would not be able to attend the required treatment sessions
  • People who the trial doctor determines would not be able to complete the required trial assessments

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 12 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Guillaume BLIVET, REGEnLIFE SAS

Phone: +33 649 813 454

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
REGEnLIFE SAS
Registry
ClinicalTrials.gov
Start date
24 July 2023
Est. completion
1 June 2026

Where this trial is recruiting

🇫🇷 France

Primary endpoints

Evolution of patient's cognition between Day 0 and Week 26 as measured with the AD Assessment Scale-cognitive subscale (ADAS-cog) score

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 12 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov