Phase 2 Multiple Sclerosis Trial, Recruiting NCT03888924 Sponsor: S. Andrea Hospital Condition: Multiple Sclerosis
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Phase 2 Multiple Sclerosis Trial, Recruiting

NCT03888924
Recruiting Phase 2

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:

  • You are male or female, of any race, and are over 18 years old.
  • You have been diagnosed with a condition called RIS (Radiologically Isolated Syndrome — an incidental finding on brain scans that may be related to MS) within the last five years.
  • You are willing and able to sign a consent form agreeing to take part.

Who may not be able to join:

  • You are currently pregnant or breastfeeding.
  • You have used immune-suppressing or immune-modifying medications in the last five years (occasional use of corticosteroids/steroids may be acceptable — confirm with trial site).
  • You have a serious or unstable health condition that could make it unsafe to participate, such as heart, lung, liver, kidney, or metabolic problems, certain infections, cancer, or immune system disorders (confirm with trial site).
  • You have a mental or physical health condition that might affect your ability to give consent or fully complete the trial, or your doctor feels you are otherwise not a suitable candidate.
  • You are unable to have an MRI scan.
  • You are currently receiving radiotherapy.
  • You have a known allergy to any ingredient in the vaccine being studied.
  • You have previously had a bone marrow stem cell transplant or an organ transplant.
  • You have received any other vaccine in the four weeks before joining the trial.

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 27 July 2026
Phase 2: approximately ~30% 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

Principal Investigator: Giovanni Ristori, S.Andrea Hospital, University of Roma La Sapienza

Phone: +390633776044

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 2
Sponsor
S. Andrea Hospital
Registry
ClinicalTrials.gov
Start date
17 June 2019
Est. completion
1 July 2026

Where this trial is recruiting

🇮🇹 Italy

Primary endpoints

cumulative number of CUAL (new gadolinium T1-weighted lesions and non-enhancing new and newly enlarging T2-weighted lesions) on MRI scans over 1 year.

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: 27 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