MRI scans aim to predict tysabri success in MS patients
NCT ID NCT02904876
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at whether special MRI scans can detect early brain changes in people with multiple sclerosis who are starting treatment with Tysabri. Researchers planned to follow 70 patients for two years, comparing MRI images before and after treatment. The goal was to find imaging markers that could predict how well someone responds to the drug. However, the study was terminated early, so the full results are not available.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Tysabri (natalizumab)
- What this could lead to
- If successful, this could help doctors predict which MS patients will respond well to Tysabri using MRI scans.
- What could go wrong
- The study was terminated early, so results are limited. It was also small and exploratory, meaning findings may not be conclusive or widely applicable.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
-
70 people
The number who actually took part.
- Started
-
Mar 2015
- Finished
-
May 2020
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Major Patient * Patient with relapsing remitting multiple sclerosis and eligible for treatment with Tysabri * Patient affiliated to a social security scheme * Patient who signed informed consent * Patient who have been informed of the results of the prior medical examination Exclusion Criteria: * Patient not currently eligible for treatment with Tysabri * Contraindication to MRI scanning * Unability to provide informed consent (subject in an emergency situation, difficulties in understanding , ...) * Patient under judicial protection * Patient under guardianship or curatorship * Pregnancy (women of childbearing age in the absence of effective contraception) * Breastfeeding
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Service de Neurologie Hôpital de Hautepierre
Strasbourg, Alsace, France
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Other studies related to the condition(s) this trial covers.
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