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This trial is complete. It is no longer accepting participants. Results may be available on ClinicalTrials.gov.

NCT01767701

NCT01767701
Completed Phase 2

Who may be able to join

Who might be able to join this trial:

  • You are between 18 and 55 years old.
  • You have been diagnosed with Multiple Sclerosis (MS) according to specific 2010 diagnostic guidelines.
  • Your MS disability level falls within a certain range, as measured by a standard MS scoring scale (confirm with trial site).
  • You have had at least one MS relapse (flare-up) in the past 12 months, or a specific type of active lesion was found on a brain scan within the last 3 months.
  • An active lesion was visible on your screening brain scan, if a brain scan was used to check your eligibility.
  • If you are a woman who could become pregnant, you must agree to use an effective form of contraception from the time you consent until 6 weeks after finishing treatment.
  • If you are a woman who could become pregnant, you must have a negative pregnancy test before each brain scan or within 7 days before starting the study.
  • You are willing and able to sign a consent form agreeing to take part and allow your health information to be used.
  • You are willing and able to provide blood, saliva, and urine samples at regular points throughout the study.
  • You are willing and able to have contrast-enhanced brain scans (MRI scans using a special dye) at regular points throughout the study.
  • You are able to follow all the requirements of the study.

Who may not be able to join:

  • You are currently pregnant, breastfeeding, or are not willing to use contraception.
  • You have taken immune-suppressing, immune-modifying, or experimental medications in the last 6 months (short-course steroids for MS relapses may be an exception — confirm with trial site).
  • You have taken steroid treatment (by mouth or injection) in the 30 days before your initial study assessment.
  • You have a serious or unstable medical condition, such as poorly controlled diabetes, high blood pressure, heart problems, abnormal liver tests, or certain abnormal blood count results (confirm with trial site).
  • You have tested positive for HIV.
  • You are currently taking a type of medication called a proton pump inhibitor, such as omeprazole or esomeprazole (used for acid reflux or stomach ulcers).
  • You have active hepatitis B or C with abnormal liver test results above a certain level.
  • You have taken part in another clinical drug trial within the last 30 days.
  • You have a history of cancer, unless a special exception is approved by the lead researcher.
  • You have had a problem with uncontrolled drug or alcohol use within the 6 months before joining the study.
  • You have been treated with a medication called Rifampicin (an antibiotic) in the last 4 weeks.

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.

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.

Trial details

Status
Completed
Phase
Phase 2
Sponsor
Queen Mary University of London
Registry
clinicaltrials_gov
Start date
1 April 2013
Est. completion
1 September 2014

Where this trial is recruiting

🇬🇧 United Kingdom

Primary endpoints

The Number of New or Recurrent Gd-enhancing Lesions That Appear on Brain T1-weighted MRI

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: 30 June 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

View original record on ClinicalTrials.gov