Phase 4
N=259
Discontinuation of Disease Modifying Therapies (DMTs) in Multiple Sclerosis (MS)
Multiple Sclerosis
Bottom Line
View on ClinicalTrials.gov: NCT03073603 ↗Enrolled (actual)
259
Serious AEs
0.8%
Results posted
Oct 2022
Primary outcome: Primary: Number of Participants Developing a New MS Relapse and/or MRI Brain Lesion Over the Course of the Study Duration — 6; 16 Participants — p=0.521
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 4
- Interventions
- Discontinuation of disease modifying therapy (Drug); Standard of Care (Drug)
- Age
- Adult, Older Adult · 55+ yrs
- Sex
- All
- Sponsor
- University of Colorado, Denver
- Primary completion
- Aug 2021
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Number of Participants Developing a New MS Relapse and/or MRI Brain Lesion Over the Course of the Study Duration |
6; 16 | 0.521 |
| SECONDARY Number With Disability Progression Confirmed at 6 Months Using the Expanded Disability Status Scale (EDSS) |
14; 16 | 0.766 |
| SECONDARY Change in Neuro-QoL (Quality of Life) Short Form Scores -- Upper Extremity Function |
-1.1; -0.6 | 0.604 |
| SECONDARY Change in Neuro-QoL (Quality of Life) Short Form Scores -- Lower Extremity Function |
-0.2; -1.1 | 0.198 |
| SECONDARY Change in Neuro-QoL (Quality of Life) Short Form Scores -- Fatigue |
-0.1; -0.9 | 0.354 |
| SECONDARY Change in Neuro-QoL (Quality of Life) Short Form Scores -- Sleep Disturbance |
-0.3; -0.5 | 0.831 |
| SECONDARY Change in Neuro-QoL (Quality of Life) Short Form Scores -- General Concerns |
0.6; 1.5 | 0.252 |
| SECONDARY Change in Neuro-QoL (Quality of Life) Short Form Scores -- Executive Function |
0.3; 0.3 | 0.983 |
| SECONDARY Change in Neuro-QoL (Quality of Life) Short Form Scores -- Communication |
0.1; -0.4 | 0.155 |
| SECONDARY Change in Neuro-QoL (Quality of Life) Short Form Scores -- Anxiety |
0.2; 0.4 | 0.748 |
| SECONDARY Change in Neuro-QoL (Quality of Life) Short Form Scores -- Depression |
0.9; 1.1 | 0.773 |
| SECONDARY Change in Neuro-QoL (Quality of Life) Short Form Scores -- Positive Affect and Well-Being |
0; -1.2 | 0.224 |
| SECONDARY Change in Neuro-QoL (Quality of Life) Short Form Scores -- Emotional-Behavioral Dyscontrol |
-0.2; -0.3 | 0.962 |
| SECONDARY Change in Neuro-QoL (Quality of Life) Short Form Scores -- Satisfaction With Social Roles and Activities |
1.7; -0.7 | 0.005 sig |
| SECONDARY Change in Neuro-QoL (Quality of Life) Short Form Scores -- Ability to Participate in Social Roles and Activities |
-2.8; -1.6 | 0.406 |
| SECONDARY Change in SymptoMScreen Composite Score (SymptoMScreen - Overall Symptom Severity). |
0; 0 | 0.348 |
| SECONDARY Change in Patient-Determined Disease Steps (PDDS - Disability). |
0; 0.3 | 0.086 |
| SECONDARY Change in Symbol Digit Modalities Test (SDMT - Cognition). |
2.5; 1.8 | 0.575 |
| SECONDARY Evaluation of the Patient's Quality of Life Using the MSIS-29 Scale -- Physical Impact |
41; 45 | 0.733 |
| SECONDARY Evaluation of the Patient's Quality of Life Using the MSIS-29 Scale -- Psychological Impact |
44; 43 | 0.733 |
Summary
Natural history research in Multiple Sclerosis (MS) suggests that risk of relapses and new Magnetic Resonance Imaging (MRI) changes diminish significantly as people age, especially in MS patients 55 or older. Thus, the need to continue MS medicines that reduce relapses and new MRI lesions may also decrease as people age, especially in those who have not had relapses or MRI scan changes for prolonged times. This study plans to learn more about the safety of stopping MS medication in this population, as compared to continuing on the medication.
Eligibility Criteria
Inclusion Criteria
- Patients with either Relapsing-remitting MS (RRMS), Secondary progressive MS (SPMS), or Primary progressive MS (PPMS) by McDonald 2010 criteria.
- Patients defined by subtype based on 2013 updated phenotypic criteria.
- Progression of MS defined by the local PI either:
- prospectively with an EDSS change of at least 1.0 points over the last two years, or
- retrospectively, with any significant change in motor function over at least one year, unrelated to relapse.
- 55 years of age or older at time of randomization;
- No evidence of recent new inflammatory disease activity (inactive by the Lublin criteria16) with no new relapse for at least five years and no new MRI lesion for at least three years
- Using any of the FDA-approved MS DMTs (to include:
- interferon β-1a,
- interferon β-1b,
- glatiramer acetate,
- natalizumab,
- fingolimod,
- dimethyl fumarate,
- ocrelizumab, or
- teriflunomide; continuously for no less than 5 years.
- Taking most recent DMT continuously* for no less than two years.
- Willing to be randomized per this protocol; each patient will be questioned as to their willingness to stay in the trial regardless of the group to which group they are randomized.
- Willing to follow the protocol
- Able to undergo a brain MRI without anesthesia
- Continuously will be defined as no less than 75% of all prescribed doses, with no time of greater than four weeks from last intended dose to have missed a dose (8 weeks for natalizumab, i.e. one missed dose).
Exclusion Criteria
- Any MS relapse in the last five years, as determined at the screen visit by the PI
- Any new or definitely enlarging T2/FLAIR lesion or new gadolinium-enhancing lesion within the past three years (at least two scans separated by at least three years must be reviewed) on brain or spine MRI scan. Lesions must be 3mm or larger to be exclusionary.
- Significant (as defined by the PI) intolerance of presently-used DMT
- More than two courses of acute, systemic (IV or oral) steroids in the last 5 years or any use within the last year. Course is defined as three or more days continuously, and not to exceed 14 days. No use of chronic, systemic steroids, defined as 15 or more days, in the last 5 years. Any use of steroids to treat MS relapse, possible relapse, or pseudo-relapse in the last 5 years.
- Use of inhaled or topical steroids are not an exclusion criteria.
- Use of oral steroids for no greater than 14 days given for a non-MS condition is not exclusionary.
- Prior use of the following in the past 5 years:
- alemtuzumab,
- mitoxantrone,
- cyclophosphamide,
- methotrexate,
- cyclosporine,
- rituximab,
- siponimod, or
- cladribine
- Prior use of any experimental agent used as a DMT for MS in the last five years
- Other significant medical or psychiatric illness, if uncontrolled. Examples:
- uncontrolled hypertension,
- uncontrolled diabetes,
- uncontrolled asthma, or
- uncontrolled depression
- Cancers other than basal cell skin cancers within the last 5 years
- Unable to give informed consent or follow the protocol
- Unable to undergo brain MRI
- Unwilling to be randomized per this protocol
- History of other chronic neurological illnesses that might mimic MS with chronic or intermittent symptoms (i.e. ALS, myasthenia gravis, chronic neuropathy, etc.)
Data sourced from ClinicalTrials.gov (NCT03073603). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.