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Multiple Sclerosis, Dimethyl Fumarate, Diffusion Tensor Imaging Magnetic Resonance ImagingDTINCT02686684

Tecfidera Diffusion Tensor Imaging

An observational study of Multiple Sclerosis, Dimethyl Fumarate, Diffusion Tensor Imaging Magnetic Resonance Imaging, run by University at Buffalo.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The primary aim of this study is to explore the effect of dimethyl fumarate on gray matter (GM) pathology, as measured by changes in diffusion-tensor imaging (DTI) of the thalamus in patients with relapsing multiple sclerosis (MS). Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
What is being tested?
Dimethyl fumarate
How many people
115 participants
Where
No sites listed yet
Study dates
Nov 2015to Oct 2016
Phase
Observational
Are there results?
None posted in the registry

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 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Study population: Seventy-five (75) consecutive relapsing MS patients who started treatment with dimethyl fumarate and 40 healthy controls will be recruited in the study.

Who may be able to join

  • MS patients diagnosed with MS according to the McDonald criteria
  • MS patients having a relapsing disease course
  • Starting treatment with dimethyl fumarate therapy for at least one month
  • Having standard of care 1.5T or 3T MRI scan obtained at baseline (time of start of dimethyl fumarate) and at the 12 and 24 months after starting dimethyl fumarate. In case of healthy controls, having 2 MRI scans with a minimum of 24 months apart
  • Have DTI sequence at all timepoints
  • At least 18 years of age
  • None of the exclusion criteria

Who cannot join

  • Patients who had a relapse within 30 days prior to MRI scan date
  • Patients who received steroid treatment within 30 days prior to the MRI scan date
  • Women who were pregnant during the time of the retrospective study or are pregnant/lactating at the time of the prospective arm
  • All healthy controls will be part of the retrospective arm.

About this study

Official title: An Open-label, Observational, Single-blinded, Longitudinal Study to Evaluate the Effect of Dimethyl Fumarate on Gray and White Matter Pathology in Subjects With Relapsing Multiple Sclerosis

The primary aim of this study is to explore the effect of dimethyl fumarate on gray matter (GM) pathology, as measured by changes in diffusion-tensor imaging (DTI) of the thalamus in patients with relapsing multiple sclerosis (MS). The secondary objective of this study is to investigate the effect of dimethyl fumarate on evolution of microstructural changes in normal appearing white matter (NAWM), as measured by DTI.

Read the detailed description

Multiple sclerosis (MS) is a central nervous system (CNS) autoimmune disorder characterized by chronic inflammation, axonal demyelination, and neuronal degeneration. The complex pathophysiology of MS is mediated by autoreactive T cells that ultimately invade and attack the CNS by traversing the blood-brain barrier (BBB), resulting in persistent irreversible axonal damage and physical disability. Magnetic resonance imaging (MRI) metrics contribute substantially to the diagnosis and management of MS, providing critical information regarding disease activity in addition to serving as secondary endpoint measures for clinical trials evaluating MS therapies. Traditional MRI techniques (e.g., contrast enhanced [CE] T1-weighted imaging, spin-echo [SE] T2-weighted imaging [T2-WI]) have proven effective for detecting the presence of macroscopic white matter (WM) MS lesions but are limited by the inability to effectively delineate microscopic tissue damage occurring in normal-appearing white matter (NAWM) and microscopic and macroscopic tissue damage in normal-appearing gray matter (NAGM). Furthermore, the brain-lesion burden on traditional MRI scans correlates only modestly with clinical disease progression. Thus, a need exists to use alternative non-conventional MRI techniques and approaches that more accurately monitor clinical disease activity and efficacy of disease-modifying therapies.

Dimethyl fumarate (Biogen Idec, Inc, Cambridge, MA, USA) is an FDA approved oral treatment for relapsing MS. One phase II and 2 phase III randomized, placebo-controlled and double-blinded clinical trials established that dimethyl fumarate significantly reduces relapse rates and improves disability along with neuroradiologic outcomes relative to placebo.

There is growing evidence to suggest that oxidative stress has a significant role in the pathogenesis of MS. Therapies that reduce oxidative stress, as well as inflammation, are of increasing interest. Fumaric acid esters are known to activate anti-oxidative pathways, as well as modulate the inflammatory cascade. Several in vivo studies have shown that nuclear factor E2-related factor 2 (Nrf2) has a role in attenuating proinflammatory stimuli through the modulation of cytokine signaling and through its involvement in glutathione homeostasis. For example, in one animal study, Nrf2-deficient mice were found to have increased expression of proinflammatory mediators, including cyclooxygenase-2, interleukin (IL)-1b, IL-6 and tumour necrosis factor-a, compared with wild-type mice. Nrf2 is also established as the guardian of redox homeostasis and has been shown to be critical for attenuating oxidative stress. Under oxidative conditions, Nrf2 enters into and accumulates within the nucleus of cells and activates the expression of a battery of cytoprotective and detoxification genes. A number of in vitro and in vivo studies have consistently demonstrated the key role of the Nrf2 signaling pathway in protecting the CNS from oxidative stress-related damage. Currently, oral dimethyl fumarate is the only agent that appears to directly target Nrf2, which it does by inducing the cleavage of kelch-like erythroid cell-derived protein with "cap'n'collar" homology-associated protein 1 (Keap1) from Nrf2 in the cell cytoplasm. By cleaving this Keap1-Nrf2 complex, Nrf2 is free to cross the nuclear membrane and interact with other nuclear transcription factors to upregulate the antioxidant response element. Via this mechanism, dimethyl fumarate appears to have a distinct dual mechanism of action in attenuating oxidative stress as well as in reducing inflammatory response.

Dimethyl fumarate showed robust effect in suppressing the appearance of new CE, T2 hyperintense and T1 hypointense lesions along with their volumes. In a recent study, dimethyl fumarate also exerted potential for cytoprotection and remyelination, as evidenced by changes in magnetization transfer ratio. However, the dimethyl fumarate effect on non-conventional MRI metrics, such as diffusion-tensor imaging (DTI) has not been explored.

Being tested
Dimethyl fumarate
Medical subject headings
Multiple Sclerosis

What participants receive

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

  • Dimethyl fumarateDrug

Study groups in NCT02686684
Study groupRoleWhat they receive
Dimethyl FumarateMS patients who started treatment with dimethyl fumarate
Receives: Drug: Dimethyl fumarate
Healthy ControlNot described

What is being measured

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

  1. Change in thalamus pathology as measured by FIRST analysis

    Measured: Change between baseline and 24 months

Secondary outcomes (1)
  1. Change in normal appearing white matter (NAWM) pathology as measured by SIENAX v2.6

    Measured: Change between baseline and 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 posted19 Feb 2016 (estimated)
  2. Study startNov 2015
  3. Primary completionOct 2016
  4. Study completionOct 2016

Resources

More details

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

Study design
Study type
Observational
Observational model
Case-control
Enrolment
115 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02686684
Sponsor's protocol ID
T-DTI
Acronym
DTI
Status last verified
Oct 2016
First submitted
11 Feb 2016
Last updated
26 Oct 2016
Results posted
No
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

An observational study of Multiple Sclerosis, Dimethyl Fumarate, Diffusion Tensor Imaging Magnetic Resonance Imaging, run by University at Buffalo.

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 7 inclusion and 4 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: finished, as of the sponsor's last update on 26 Oct 2016. Status can change between updates, so confirm with the study contact before making plans.

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.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

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?

Change in thalamus pathology as measured by FIRST analysis (time frame: Change between baseline and 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 26 Oct 2016; AzTrials last refreshed its copy on 27 Oct 2026.

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