Phase 3 Multiple Sclerosis Trial, Not Yet Recruiting NCT06663189 Sponsor: University Hospital, Strasbourg, France Condition: Multiple Sclerosis
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Phase 3 Multiple Sclerosis Trial, Not Yet Recruiting

NCT06663189
Not Yet Recruiting Phase 3

voxsanity.com.au · Eligibility summary from public government registries · 18 August 2026 · not medical advice

Who may and may not 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 may be able to join

  • People aged 55 or older (male or female)
  • People who have been diagnosed with relapsing-remitting multiple sclerosis (RRMS) according to specific diagnostic guidelines (McDonald 2017 criteria)
  • People whose first MS symptom appeared more than 5 years ago, or if that date is unknown, people who received their RRMS diagnosis more than 5 years ago
  • People whose MS has been stable for the last 5 years, meaning: no new lesions on brain scans (MRI) compared to a scan from at least 5 years ago, a stable disability score over the same period as assessed by a doctor, and no relapses in the last 5 years
  • People who have been continuously treated with a moderate-strength MS medication for at least 5 years — this includes interferon-beta, glatiramer acetate, dimethyl fumarate, teriflunomide, or diroximel fumarate (switching between these medications for personal reasons or due to side effects is acceptable)
  • People who are enrolled in a social security scheme (confirm with trial site, as this appears to be a French regulatory requirement)
  • People who are able to understand the goals and risks of the study and are willing to give their informed consent
  • People who are willing and able to follow all study procedures for the full duration of the trial

Who may not be able to join

Each point below is a reason the trial team may not be able to accept someone. It is not a list of requirements to meet.

  • People who have a type of MS other than relapsing-remitting, such as primary progressive MS or secondary progressive MS (with or without relapses)
  • People who have previously been treated with, or are currently taking, a high-strength MS medication — with an exception for certain intensive treatments (mitoxantrone, stem cell transplantation, or alemtuzumab) if the last dose was given at least 10 years before joining the trial
  • People for whom an MRI scan would not be safe or possible, for example due to claustrophobia, weight of 140 kg or more, a pacemaker, cochlear implants, metal fragments in the eye, certain surgical clips in the brain, or recent surgery or coronary stent placement (note: an inability to receive the contrast dye used in some MRI scans does not prevent participation — the scan can be done without it)
  • People who have a history of another neurological or brain-related disease, such as a hereditary degenerative brain condition, a degenerative memory condition, a systemic autoimmune disease, sarcoidosis, or Lyme disease
  • People who have a long-term condition that requires ongoing treatment with steroids or immune-suppressing medications
  • People with uncontrolled heart, kidney, or liver disease
  • People who are currently taking part in another clinical trial involving a drug or medical device, or who are within a required waiting period after a previous trial
  • People who wish to stop their current MS background medication, regardless of whether they are experiencing side effects
  • People who do not wish to stop their current MS background medication, regardless of whether they are experiencing side effects
  • People who are pregnant or breastfeeding
  • People who have difficulty reading or understanding French
  • People who are under a legal protection order (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 29 July 2026

Contact this trial

Principal Investigator: Nicolas COLLONGUES, MD, PhD, University Hospital, Strasbourg, France

Phone: 03 3 88 11 54 15

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
Not Yet Recruiting
Phase
Phase 3
Registry
ClinicalTrials.gov
Start date
1 January 2025
Est. completion
1 January 2027

Where this trial is recruiting

🇫🇷 France

Primary endpoints

Time to first clinical and/or radiological disease activity during a period of 2 years.

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: 29 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