Multiple Sclerosis Trial, Recruiting NCT06280742 Sponsor: Assistance Publique - Hôpitaux de Paris Condition: Multiple Sclerosis
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Multiple Sclerosis Trial, Recruiting

NCT06280742
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 Relapsing-Remitting Multiple Sclerosis (RRMS):

  • You are between 18 and 55 years old
  • You have been diagnosed with RRMS using standard diagnostic guidelines (2017 McDonald criteria)
  • Your MRI scan shows at least 9 MS-related spots in the brain
  • You have not received a steroid treatment called methylprednisolone in the last month before the study scans
  • You are not currently taking any MS medication
  • Your doctor has recommended you start a strong MS treatment (such as Natalizumab, an anti-CD20 antibody, Alemtuzumab, a sphingosine-1 phosphate modulator, or cladribine), either because your MS is very active or because you had two or more relapses in the past year
  • You are covered by a French social security or health insurance scheme (certain types of medical aid are excluded — confirm with trial site)

For healthy volunteers:

  • You are between 18 and 55 years old
  • You do not have any ongoing or progressive health conditions
  • You are able to understand the goals and procedures of the study
  • You are covered by a French social security or health insurance scheme (certain types of medical aid are excluded — confirm with trial site)

Who may not be able to join:

For all participants:

  • You have any reason that prevents you from having an MRI scan, such as claustrophobia, a pacemaker, or a metal fragment in your eye
  • You have had any medical test involving radioactivity in the last 12 months
  • A specific genetic test taken at the screening visit shows you have a "low affinity binding" profile related to a particular protein (confirm with trial site)
  • You are pregnant, breastfeeding, or are a woman who could become pregnant and is not using effective contraception
  • You currently have serious or uncontrolled problems with your kidneys, liver, blood, digestive system, lungs, heart, or any other long-term neurological condition
  • You would not want to be told if an unexpected and medically significant problem were found on your MRI
  • You are under any form of legal guardianship or protection
  • You are currently taking part in another clinical trial, or you are still within a waiting period after a previous trial

Additional exclusions for RRMS patients only:

  • You have a known allergy to gadoteric acid, meglumine, or any medication containing gadolinium (these are contrast dyes used in MRI scans)
  • You have severely reduced kidney function (based on specific blood test measurements — confirm with trial site)

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 23 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

Phone: 0171970659

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
16 December 2025
Est. completion
1 December 2028

Where this trial is recruiting

🇫🇷 France

Primary endpoints

To quantify the smoldering component of white matter lesions in people with MS, as compared with [18F]-DPA-714 binding in the white matter of HC who underwent a PET a acquisition with the same camera camera than patients in each center.

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: 23 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