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Switching MS treatments after a relapse: does it reduce future attacks?

NCT ID NCT07743281

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Aug 03, 2026 · Last updated Aug 04, 2026 · Updated 1 time

Summary

This study examines what happens when people with multiple sclerosis (MS) experience a relapse while on a standard treatment. It compares those who switch to a stronger, high-efficacy treatment with those who stay on their current therapy, looking at how many experience further relapses. By analyzing real-world data from 753 patients, the study aims to see if escalating treatment after a relapse is linked to better outcomes. The findings could help doctors and patients make more informed decisions about treatment changes.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

What this could lead to
If this study finds that escalating to a stronger treatment after a relapse reduces future relapses, it could help guide doctors in making more effective treatment decisions for people with multiple sclerosis.
What could go wrong
This is a retrospective study, meaning it looks back at past data rather than testing a new treatment in a controlled trial. It can only show associations, not proof, and results may be influenced by differences between the groups.

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.

Participants

753 people

The number who actually took part.

Started

Mar 2025

Finished

Jul 2025

Lead sponsor

A company

The lead sponsor is a pharmaceutical, biotech, or medical-device company.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

Adult MS patients who relapsed on a platform oral or injectable DMT in real-world practice during the patient identification period, between March 28, 2017 and July 31, 2023.

Ages

18 to 100 years

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

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion criteria: Patients in the Base Sample were required to meet the following eligibility criteria: * Incident claim for a platform oral or injectable DMT in the patient identification period (Mar 28, 2017 - Jul 31, 2023). * Treatment initiation date is the first qualifying DMT claim date. * Initial treatment is the DMT recorded on treatment initiation date. * No claim for a different DMT used for the treatment of multiple sclerosis (MS) on the treatment initiation date. * ≥18 years of age on treatment initiation date. * ≥2 outpatient medical claims (at least 30 days apart) with a diagnosis code for MS (International Classification of Diseases, 10th Revision, Clinical Modification \[ICD-10-CM\] code: G35) in any position, with the first claim occurring in the 12 months prior to the treatment initiation date and the second claim up to 6 months after treatment initiation date, or ≥1 inpatient claim with a diagnosis of MS in the first position in the 12 months prior to or on treatment initiation date. * ≥1 relapse recorded after ≥3 months of persistent use of initial treatment and during period of persistence on initial treatment. o Index relapse date is the start date of earliest qualifying relapse episode in the initial treatment period. * Continuous healthcare plan enrollment for ≥12 months prior to treatment initiation date and ≥12 months after index relapse date. Patients in Cohort 1 and Cohort 2 included patients meeting the following criteria: * Included in Base Sample. * ≥1 claim for a platform oral, platform injectable, or high-efficacy DMT during the switch eligibility period (12-month period after index relapse date). o For the high-efficacy DMT patients, index treatment date is the date of the first claim for a high-efficacy DMT during the switch eligibility period. For patients who remain on the initial treatment or switch to another DMT, the index treatment date is the date of the claim for the initial treatment that falls in the exposure set and meets matching criteria. * Continuous healthcare plan enrollment and persistent use of index DMT for ≥6 months after index treatment date. Exclusion criteria: • Patients who did not meet the inclusion criteria.

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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

  • Novartis

    East Hanover, New Jersey, 07936, United States

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