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

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

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03368677
Acronym
TERIPET
Enrollment
26
Registered
2017-12-11
Start date
2017-12-01
Completion date
2027-12-31
Last updated
2025-04-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Multiple Sclerosis

Brief summary

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

Detailed description

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.

Interventions

None listed

Sponsors

Turku University Hospital
Lead SponsorOTHER_GOV

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
40 Years to 55 Years
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Change of 11C-PK11195-radioligand binding using PET0 to 12 monthsChange in microglia-activity in late RRMS patients on teriflunomide treatment during one-year interval as measured by PET imaging and \[11C\]PK11195 radioligand.

Secondary

MeasureTime frameDescription
MRI metrics0, 12 months, 24 months, 36 monthsTo evaluate lesion load of the white matter MS plaques
EDSS0, 12 months, 24 months, 36 monthsExpanded Disability Status Scale
BICAMS0, 36 monthsBrief International Cognitive Assessment for MS

Countries

Finland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026