Phase 3 Multiple Sclerosis Trial, Recruiting NCT07325292 Sponsor: Sanofi Condition: Multiple Sclerosis
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Phase 3 Multiple Sclerosis Trial, Recruiting

NCT07325292
Recruiting Phase 3

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:

Group A — Relapsing MS (RMS):

  • People aged 18 to 55 years old at the time of signing the consent form.
  • People who have been diagnosed with relapsing MS, confirmed using the 2017 revised McDonald diagnostic guidelines.
  • People whose disability level, measured by a standard MS scoring tool, is at or below a certain threshold at the first study visit (confirm with trial site).
  • People who have had at least one MS relapse in the past year, OR two relapses in the past two years, OR at least one area of active inflammation visible on an MRI scan in the past year.

Group B — Non-relapsing Secondary Progressive MS (nrSPMS):

  • People aged 18 to 60 years old at the time of signing the consent form.
  • People who were previously diagnosed with relapsing-remitting MS under the 2017 revised McDonald guidelines, and who now have a diagnosis of secondary progressive MS.
  • People whose MS disability has been documented to have worsened during the 12 months before joining the study.
  • People who have had no MS relapses for at least 24 months.
  • People whose disability score on a standard MS scale falls within a specific range at the first study visit (confirm with trial site).

All participants:

  • People who are able to use an acceptable form of contraception as required by local guidelines for clinical trial participants.

Who may not be able to join:

  • People who have been diagnosed with primary progressive MS under the 2017 revised McDonald criteria.
  • People who have a current infection, a recent fever within 28 days before the screening visit, or a history of conditions that may increase the risk of serious infection.
  • People who have a history of a psychiatric condition or substance misuse.
  • People who have a history of, or are considered at significant risk of, blood clots, heart attack, stroke, or a related clotting condition, or who require blood-thinning medication.
  • People who have low levels of certain protective proteins in the blood (immunoglobulins) at screening, or who have a history of a condition causing low immunoglobulin levels.
  • People who have, or have had, another condition whose symptoms can look similar to MS symptoms.
  • People who are unable to have an MRI scan for any reason.

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 16 July 2026
Phase 3: approximately ~65% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Phone: 800-633-1610

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
Phase 3
Sponsor
Registry
ClinicalTrials.gov
Start date
14 January 2026
Est. completion
15 July 2027

Where this trial is recruiting

🇧🇪 Belgium 🇨🇳 China 🇯🇵 Japan 🇺🇸 United States

Primary endpoints

Area under the curve over the interval W20 to W24(part A); Trough concentration at steady state(part A)

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: 16 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