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Multiple SclerosisPhase 3STOP-I-SEPNCT03653273

Disease Modifying Therapies Withdrawal in Inactive Secondary Progressive Multiple Sclerosis Patients Older Than 50 Years (STOP-I-SEP)

A Phase 3 study testing DMT withdrawal and DMT continuation in people with Multiple Sclerosis, run by Rennes University Hospital at 27 sites in France.

Active, not recruiting

Under way, not looking for participants. Everyone needed has enrolled. The study is still running.

Official record
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Trial summary

Further controlled and randomized prospective studies in Multiple sclerosis, analyzing the potential impact of treatment discontinuation on disability progression, focal disease activity and quality of life are needed. Read more about this study

Who is it for?
Ages 50 years and older
Conditions the study is for
Multiple Sclerosis
What is being tested?
DMT withdrawal and DMT continuation
Could I receive a placebo?
No, everyone receives an active treatment
How many people
250 participants
Where
27 sitesFrance
Study dates
24 Jan 2019to Jul 2027
Phase
Phase 3
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 50 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Patients > 50 years old;
  • Secondary progressive phenotype for at least 3 years; The secondary progressive phenotype will be defined as progressive deterioration of disability not due to relapse, with an increase of at least 1 EDSS point since the beginning of the progressive phase (or 0.5 EDSS point if EDSS score ≥ 5.5).
  • Disease modifying therapy of MS for at least 3 years (interferon, glatiramer acetate, teriflunomide, dimethyl fumarate, cyclophosphamide, azathioprine, methotrexate, mycophenolate mofetil, rituximab, ocrelizumab); Both patients with the same DMT or with successive DMTs during 3 years can be included. It is important to note that patients could have been treated with fingolimod or natalizumab 2 or 3 years before inclusion, but not during the year before inclusion ;
  • No evidence of focal inflammatory activity for at least 3 years (no clinical relapse and no gadolinium enhancement on an MRI scan);
  • EDSS≥3.
  • Concomitant medications with Fampridine are allowed throughout the study, provided they have been introduced at least 1 months before inclusion.
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  • Natalizumab and fingolimod during the year before inclusion were excluded because of the risk of recurrence of inflammatory activity or even rebound of inflammatory activity after withdrawal.
  • Both patients with the same DMT or with successive DMTs during 3 years can be included, as for example, cyclophosphamide is used for 1 or 2 years, sometimes followed by mycophenolate mofetil.
  • For Rituximab and Ocrelizumab, inclusion in STOP-I-SEP will be at 6 months from the last infusion to take into account the mode of action of these treatments and their specific administration scheme.

Who cannot join

  • Patients treated with mitoxantrone or alemtuzumab, during the previous 3 years before inclusion;
  • Patients treated with natalizumab or fingolimod during the year before inclusion;
  • Change of disease modifying therapy of MS for less than a year
  • Other neurological or systemic disease ;
  • Incapacity to understand or sign the consent form ;
  • Contraindication to MRI ;
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  • Pregnancy or breast-feeding ;
  • Patient in another clinical trial
  • Persons referred to in Articles L. 1121-5 to L. 1121-8 and L. 1122-1-2 of the Public Health Code (eg minors, protected adults, …).

Trial locations and contacts

27 sites in 1 country.

27 sites in 1 country

France27 sites
  • CHU Angers

    Angers

  • CHU de Bordeaux

    Bordeaux

  • CHU Brest

    Brest

  • CH de Chartres

    Chartres

  • CHU Clermont-Ferrand

    Clermont-Ferrand

  • Hôpital Henri Mondor

    Créteil

  • CHU Dijon

    Dijon

  • CHU Grenoble

    Grenoble

  • CH de Libourne

    Libourne

  • CHU Lille

    Lille

  • Hôpital Saint Vincent de Paul

    Lille

  • Hospices Civils Lyon

    Lyon

  • AP-HM

    Marseille

  • CHU Montpellier

    Montpellier

  • CHU Nancy

    Nancy

  • CHU Nantes

    Nantes

  • CHU Nice

    Nice

  • CHU de Nîmes

    Nîmes

  • AP-HP (La Pitié Salpêtrière)

    Paris

  • Fondation de Rothschild

    Paris

  • CH Poissy

    Poissy

  • CHU Poitiers

    Poitiers

  • CH Quimper

    Quimper

  • CHU Rennes

    Rennes

  • CHU Strasbourg

    Strasbourg

  • CH de Foch

    Suresnes

  • CHU Tours

    Tours

Other trials in France

About this study

Official title: Disease Modifying Therapies Withdrawal in Inactive Secondary Progressive Multiple Sclerosis Patients Older Than 50 Years

Further controlled and randomized prospective studies in Multiple sclerosis, analyzing the potential impact of treatment discontinuation on disability progression, focal disease activity and quality of life are needed. The optimum patient age and duration of inactive SPMS before treatment withdrawal and the monitoring procedures also need to be specified, the ultimate goal being to provide evidence-based recommendations for clinical practice. Following the previous retrospective experience, we decided to drive a multicenter prospective study in France based on the hypothesis that stopping disease modifying therapy will not induce an increased risk of disability progression and relapse in selected SPMS patients (older patients without lesion activity) but will improve the quality of life and may reduce treatment-related costs.

Read the detailed description

Multiple sclerosis (MS) usually evolves over decades and can present several phenotypes. Approximately 85% of newly diagnosed Multiple Sclerosis (MS) patients present the Relapsing-Remitting MS (RRMS) phenotype. After a mean time of approximatively 20 years, a large majority of these patients evolve to the so-called "Secondary Progressive MS" (SPMS) phase. SPMS is characterized by an irreversible disability progression not related to relapses, although relapses could be superimposed. Nevertheless, the shift in-between RRMS and SPMS is not clear. Different subtypes of SPMS have been recently defined by F Lublin et al. This classification takes into account persistent focal inflammatory activity (active vs inactive SPMS) along with disease progression (progressing vs non-progressing SPMS). In clinical routine, it is important to identify these stages of MS as they differently respond to the disease modifying therapies (DMTs).

Introducing DMTs during the RRMS phase had consistently demonstrated a significant impact on the annual relapse rate (ARR) and on the short-term disability progression. Conversely, during the SPMS phase, the impact of DMTs remained uncertain on disability progression, especially in older patients, with "inactive" disease. As a matter of fact, the DMTs are considered to be anti-inflammatory by nature, but the focal inflammation reduces with age and disease duration.

In addition, the DMTs have side effects and cost approximately 10,000 euros per year and per patient. In this context, the usefulness of continuing DMTs in "inactive" SPMS patients older than 50 years is questionable.

In a preliminary retrospective study conducted at our Institute which enrolled 100 SPMS patients, the ARR remained stable 3 years after treatment withdrawal (0.07, 95% CI [0.05, 0.11]), relative to the 3 years prior to treatment withdrawal (0.12, [0.09, 0.16]). EDSS scores were available for 94 patients The percentage of patients experiencing a significant increase of their EDSS score during the 3 years after treatment withdrawal also remained stable compared to the 3 years prior treatment withdrawal. These preliminary data support the safety of DMTs withdrawal in selected SPMS patients. However, further prospective studies are needed to provide evidence-based guidelines for daily practice.

This randomized controlled clinical trial thus aims to compare SPMS patients older than 50 years without evidence of focal inflammatory activity for 3 years, stopping DMTs versus patients with the same criteria still receiving treatment. We hypothesize that stopping DMTs will not induce an increased risk of disability progression or relapse in SPMS patients but will improve their quality of life and have an impact on treatment-related costs.

So far, the impact of DMTs withdrawal in a selected SPMS population has not been explored. Having evidence-based recommendations on the treatment management of these patients is essential, considering the consequences in terms of disability, relapses, side effects, quality of life and costs. DMTs in MS are now available since 20 years, with an increasing number of approved molecules. As a matter of fact, this question concerns a large number of patients: a retrospective analysis of patients included in the Rennes EDMUS database allowed to identify 71 SPMS patients older than 50 years and without evidence of focal inflammatory activity for 3 years actually undergoing a DMT.

For evident conflict of interests, the pharmaceutical firms will not promote or fund clinical trials on treatment withdrawal. A randomized controlled study initiated by academia and financed by public funding should be performed to explore these questions. We will evaluate the impact of these changes from the patient and the health system's points of view. The results of this clinical trial will lead to a concrete change in clinical practice.

Being tested
DMT withdrawal, DMT continuation
Keywords
multiple sclerosis, secondary progressive, disease modifying treatment, medico economic impact, treatment withdrawal
Medical subject headings
Multiple Sclerosis

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • DMT withdrawalOther

    Group 1 (DMT withdrawal) will not undergo any disease modifying treatments (DMT).

  • DMT continuationDrug

    Group 2 (DMT continuation) may undergo the DMT . The therapy continued in this research is the one previously established, at the same dose, not implying additional precautions for use.

Study groups in NCT03653273
Study groupRoleWhat they receive
DMT withdrawalExperimentalDMT will be immediately stopped after randomization.These patients will be followed for 2 years.
Receives: Other: DMT withdrawal
DMT continuationActive comparatorThe previously established therapy will be continued at the same dose during two years.
Receives: Drug: DMT continuation

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Disability progression measured by EDSS

    Disability progression measured by the Percentage of patients experiencing disability progression (confirmed at 6 months) at 2 years.

    Disability progression will be defined as an increase in the EDSS of at least 1 point if the baseline EDSS was 5.5 or less, or 0.5 point if the Baseline EDSS was more than 5.5.

    Measured: 24 months

Secondary outcomes (14)
  1. Time of Disability progression

    Disability progression measured by Time from DMT withdrawal to disability progression

    Measured: 24 months

  2. Disability progression measured by composite score

    Disability progression measured by Change in a composite disability progression score (increase in the EDSS score, or an increase in the time to perform the timed 25-foot walk ≥ 20%, or an increase in the time to complete the 9-hole peg test ≥ 20%) confirmed at 6 months

    Measured: 24 months

  3. Disability progression measured by SDMT

    Disability progression measured by Change in the SDMT score from baseline to 2-year

    Measured: 24 months

  4. Percentage of patients with Relapse

    Relapses measured by Percentage of patients with at least one relapse from baseline to 2-year

    Measured: 24 months

  5. Annualized relapse rate

    Relapses measured by Annualized relapse rate during 2-year

    Measured: 24 months

  6. Time of Relapses

    Relapses measured byTime from DMT withdrawal to first relapse;

    Measured: 24 months

  7. Percentage of patients with brain lesion

    Percentage of patients with one or more new or enlarging brain MRI (Magnetic Resonance Imaging) lesions from baseline to 2-year

    Measured: 24 months

  8. Percentage of patients with gadolinium enhancing lesion

    Percentage of patients with at least one gadolinium enhancing lesion(s) at 6 months, and/or 1 year,and/or 2-year

    Measured: 24 months

  9. Change in brain volume

    Change in brain volume from baseline to 2-year measured on MRI

    Measured: 24 months

  10. Percentage of patients with no evidence of disease activity

    Percentage of patients with no evidence of disease activity (NEDA 3: no clinical relapse, no MRI activity, no disability progression) at 2-year

    Measured: 24 months

  11. Percentage of patients who resume DMT in the treatment withdrawal group

    Percentage of patients who resume DMT in the treatment withdrawal group at 2-year

    Measured: 24 months

  12. Quality of life measured by SEP-59 score

    Change in the SEP-59 score from baseline to 2-year;

    Measured: 24 months

  13. Quality of life measured by EQ-5D score

    Change in the EuroQOL EQ-5D from baseline to 2-year;

    Measured: 24 months

  14. Medico economic impact

    Incremental Cost Effectiveness Ratio (ICER) defined as the cost for QALY gained in "treatment withdrawal group" versus "treatment continued group"

    Measured: 24 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted31 Aug 2018
  2. Study start24 Jan 2019
  3. Primary completionJul 2027 (estimated)
  4. Study completionJul 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
250 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03653273
Sponsor's protocol ID
35RC17_8842_STOP-I-SEP
Acronym
STOP-I-SEP
Status last verified
Mar 2026
First submitted
28 Aug 2018
Last updated
30 Mar 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A Phase 3 study testing DMT withdrawal and DMT continuation in people with Multiple Sclerosis, run by Rennes University Hospital at 27 sites in France.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 9 inclusion and 9 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: under way, not looking for participants, as of the sponsor's last update on 30 Mar 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 27 sites in France. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Disability progression measured by EDSS (time frame: 24 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 30 Mar 2026.

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