Alzheimer's Disease Trial, Recruiting NCT06523296 Sponsor: Centre Hospitalier Universitaire de Nice Condition: Alzheimer's Disease
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Alzheimer's Disease Trial, Recruiting

NCT06523296
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:

For people with Myasthenia Gravis:

  • Adults who have been diagnosed with a specific type of myasthenia gravis (anti-AChR positive autoimmune myasthenia gravis), confirmed by clinical and lab tests, and classified in a recognised severity category (Class I to IV by the MGFA)
  • People who have been diagnosed with a mild or major neurocognitive disorder (a thinking or memory condition meeting DSM-5 standards) through a specialist memory centre (CMRR), including spinal fluid (CSF) testing, and who agree to allow leftover spinal fluid samples to be stored for research
  • People who are willing to sign an informed consent form
  • People who are enrolled in or covered by a French social security system

For people with Alzheimer's Disease:

  • Adults who have been diagnosed with a mild or major neurocognitive disorder (meeting DSM-5 standards) through a specialist memory centre (CMRR), including spinal fluid (CSF) testing, and who agree to allow leftover spinal fluid samples to be stored for research
  • People whose neurocognitive disorder has been linked solely to Alzheimer's disease, confirmed by recognised diagnostic criteria (IWG-2) and Alzheimer's-specific markers found in spinal fluid
  • People who are willing to sign an informed consent form
  • People who are enrolled in or covered by a French social security system

For healthy volunteers (control group):

  • People who have no memory complaints
  • People who have no neurocognitive disorder
  • People who have previously agreed to have their spinal fluid samples, stored at a biobank at the Institute of Translational Neurology in Münster, Germany, used for research analysis

Who may not be able to join:

For people with Myasthenia Gravis:

  • People who do not have sufficient command of the French language to understand, read, and complete neuropsychological tests
  • People whose routine spinal fluid sample is needed for other standard diagnostic tests as part of their regular medical care
  • People who fall into certain protected or vulnerable categories, including: pregnant women, women who have recently given birth, or breastfeeding mothers; people deprived of their liberty by a judicial or administrative decision; people hospitalised without their consent under specific French legal provisions; people admitted to a health or social facility for reasons other than research; and adults under a legal protection measure or who are unable to give their own consent

For people with Alzheimer's Disease:

  • People who fall into certain protected or vulnerable categories, including: pregnant women, women who have recently given birth, or breastfeeding mothers; people deprived of their liberty by a judicial or administrative decision; people hospitalised without their consent under specific French legal provisions; people admitted to a health or social facility for reasons other than research; and adults under a legal protection measure or who are unable to give their own consent

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 22 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: SACCO GUILLAUME, MD, Centre Hospitalier Universitaire de Nice

Phone: 33492034778

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
Registry
ClinicalTrials.gov
Start date
17 April 2024
Est. completion
1 May 2026

Where this trial is recruiting

🇫🇷 France

Primary endpoints

The ratio of the number of myasthenic patients with NS-NCD that may be related to myasthenia-related central nervous system damage to the total number of myasthenic patients with CND from all causes combined.

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: 22 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