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Active, Not Recruiting

NCT Number: NCT03368677

Effect of Teriflunomide Treatment on Microglial Activation in an MS Patient Cohort at Risk of Progression

To evaluate the effect of teriflunomide treatment on microglial activation in late stage multiple sclerosis.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

Key information

Age range

40 year–55 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Turku PET Centre

Turku, Southwest Finland, 20520, Finland

About this study

In Multiple Sclerosis (MS), plaques in the white and grey matter of the brain represent the best known pathological changes of the disease, but a significant inflammation process has also been detected outside these plaques in connection with the disease. This extensive, diffuse inflammatory process correlates with the progression of the disease, measured by EDSS score (Expanded Disability Status Scale status) and reduction in patients' cognitive level. According to neuropathological research, the diffuse inflammatory process outside the plaques is connected with powerful activation of microglia, oxidative stress, and deficiencies in mitochondrial activity. The activation of microglial cells can be measured in vivo in patients using positron-emission tomography (PET) scanning and so-called TSPO radioligands, such as the 11C-PK11195 radioligand. 11C-PK11195 radioligand binds to TSPO molecules, which manifest on the surface of activated, but not un-activated, microglia.

Teriflunomide treatment is expected to slow down the process of increasing microglial activation. TSPO-PET imaging allows in vivo follow-up of the pathogenic process associated with the gradual MS disease evolution, and allows to evaluate whether teriflunomide treatment has an effect on disease progression-related pathology.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Signing the consent form
  • Having used teriflunomide treatment for at least 6 months
  • 40-55 years of age at the time of signing the research consent form
  • MS diagnosis in accordance with either the Poser or McDonald criteria
  • EDSS 2-6.5
  • Clear lesion load in brain MRI (> 9 T2 lesion)

Exclusion criteria

  • Patients suffering from another brain disease of in addition to multiple sclerosis
  • Steroid treatment 4 weeks prior to the scan
  • Significant pathology in the MRI scan other than MS-related lesions
  • Patients suffering from claustrophobia or panic disorder, or patients who have exhibited hypersensitivity of PET markers (practical obstacle to the scan)
  • Exposure to experimental radioactivity in the last 12 months such that the dosimetry threshold would be exceeded due to participation in the study
  • Severe hepatic impairment
  • Pregnant women, or women of childbearing potential who are not using reliable contraception during treatment with teriflunomide and thereafter as long as its plasma levels are above 0.02 mg/l.

Treatment and study plan

Primary outcomes

  1. Change of 11C-PK11195-radioligand binding using PET

    Time frame: 0 to 12 months

    Change in microglia-activity in late RRMS patients on teriflunomide treatment during one-year interval as measured by PET imaging and [11C]PK11195 radioligand.

Secondary outcomes

  1. MRI metrics

    Time frame: 0, 12 months, 24 months, 36 months

    To evaluate lesion load of the white matter MS plaques

  2. EDSS

    Time frame: 0, 12 months, 24 months, 36 months

    Expanded Disability Status Scale

  3. BICAMS

    Time frame: 0, 36 months

    Brief International Cognitive Assessment for MS

Sponsors and collaborators

Lead sponsor

Turku University Hospital

Other Gov

Registry information

Official study title

Targeting SPMS: Effect of Teriflunomide Treatment on Microglial Activation in an MS Patient Cohort at Risk of Progression. A [11C]PK11195 Brain PET Study

Acronym: TERIPET

Important dates

Study start
2017
Primary completion
2027
Study completion
2027
First posted
Dec 11, 2017
Registry last updated
Apr 13, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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