Multiple SclerosisPROMSNCT03134716
Role of Microglia in the Pathogenesis of Progressive Multiple Sclerosis
An observational study of Multiple Sclerosis, run by Turku University Hospital at 1 site in Finland.
Trial summary
Our aim is to evaluate whether translocator binding protein (TSPO)-imaging correlates to Expanded Disability Status Scale (EDSS) and other disease progression-related clinical and paraclinical parameters in a homogenous cohort of 40-50-year old MS-patients, who are at risk of progression. Read more about this study
- Who is it for?
- Ages 40 to 50 yearsHealthy volunteers can take part
- Conditions the study is for
- Multiple Sclerosis
- How many people
- 35 participants
- Where
- 1 siteFinland
- Study dates
- Apr 2016to Dec 2026
- Phase
- Observational
- 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 40 to 50 years
- All sexes
- Healthy volunteers accepted
- Adult
Study population: Relapsing remitting MS (RRMS) patients on the verge of secondary progression, age 40-50 years, MS-diagnosis for a minimum of five years before entering the study.
Who may be able to join
- RRMS, age 40-50 years, MS-diagnosis for a minimum of five years.
Who cannot join
- Previous or present treatment with immunosuppressive medication or biologicals. - Steroid treatment within 30 days of evaluation
Trial locations and contacts
1 site in 1 country.
About this study
Our aim is to evaluate whether translocator binding protein (TSPO)-imaging correlates to Expanded Disability Status Scale (EDSS) and other disease progression-related clinical and paraclinical parameters in a homogenous cohort of 40-50-year old MS-patients, who are at risk of progression. The A2A-AR expression in this cohort will also be studied using the adenosine A2A-receptor (A2A-AR)-binding radioligand 11C-TMSX. The study cohort will also form the basis for a later follow-up study, which will be performed to evaluate the prognostic value of baseline TSPO-imaging in terms of disease progression. TSPO-imaging could thus be used as an imaging biomarker to help identifying patients to therapeutically prevent progression of MS. At the 5 year time point synaptic density will be evaluated using 11C-UCB-J radioligand and PET imaging.
Read the detailed description
Protocol title: Role of microglia in the pathogenesis of progressive multiple sclerosis
Rationale of the study: The investigators have demonstrated earlier a statistically significant correlation between TSPO-binding and EDSS in a heterogeneous MS-population comprising both early RRMS and late secondary progressive multiple sclerosis (SPMS) patients. Now the investigators aim to evaluate whether TSPO-imaging correlates to EDSS and other disease progression-related clinical and paraclinical parameters in a homogenous cohort of 40-50-year old MS-patients, who are at risk of progression. The A2A-AR expression in this cohort will also be studied using the A2A-AR-binding radioligand 11C-TMSX. The study cohort will also form the basis for a later follow-up study, which will be performed to evaluate the prognostic value of baseline TSPO-imaging in terms of disease progression. TSPO-imaging could thus be used as an imaging biomarker to help identifying patients to therapeutically prevent progression of MS. At the 5 year time point synaptic density will be evaluated using 11C-UCB-J radioligand and PET imaging.
Study population: The study population will consist of a clinically homogenous group of 25 relapsing remitting multiple sclerosis (RRMS) patients with MS-diagnosis for at least 5 years, age 40-50 years, who may be using any first-line MS therapy. The patients will be recruited from the outpatient clinic of the Division of Clinical Neurosciences of the University Hospital of Turku, Finland. In addition the investigators will image a group of 10 age- and sex-matched healthy control subjects for comparison.
Study Objectives Primary: To evaluate how TSPO-ligand binding in the normal appearing white matter (NAWM) correlates to EDSS.
Secondary: 1) To evaluate how TSPO-ligand binding in the NAWM at baseline correlates to other standard clinical and paraclinical parameters typically associated with disease progression 2) To evaluate how 11C-TMSX-binding (to A2A-AR) correlates to the clinical and paraclinical parameters, and to TSPO-binding. 3) To evaluate how synaptic density evaluated using 11C-UCB-J binding correlates to patients cognitive functions.
Inclusion criteria: RRMS, age 40-50 years, MS-diagnosis for a minimum of five years. Exclusion criteria: Previous or present treatment with immunosuppressive medication or biologicals. Steroid treatment within 30 days of evaluation Evaluation of patients: Baseline brain MRI and PET using 11C-PK11195 and 11C-TMSX with a protocol used in our previous studies. MS functional composite (MSFC), brain atrophy, quantitative diffusion tensor magnetic resonance imaging (DTI-MRI) measures, and neuropsychological status. At 5 years PET using 11C-UCB-J radioligand.
Positron emission tomography (PET) imaging methods: 1) Detection of microglial activation. The investigators shall use the TSPO-ligand 11C-PK11195 to evaluate the level of microglial activation in the NAWM, in normal appearing gray matter (NAGM) and in the periplaque areas. The 11C-PK11195 imaging. 2) A2A-AR detection. The investigators shall investigate the distribution of the A2A-ARs using PET and (11C-TMSX). This will be performed to correlate A2A-AR expression with microglial activation in the central nervous system (CNS) of RRMS patients at risk of converting to SPMS. The 11C-TMSX imaging.3) Evaluation of synaptic density using 11C-UCB-J-PET. The association between 11C-UCB-J binding and cognitive functions will be evaluated.
Based on earlier experience with PET ligands it is estimated that 15 subjects per group is enough to reveal 15% difference in 11C-PK11195 and 11C-TMSX uptake between the study groups with 90% power at p-level <0.05. The correlation analyses between the variables will be performed with Spearman's non-parametric test for non-linear, and Pearson's test for linear association.
Facilities: Turku PET Centre (TPC) is the national PET Centre in Finland. It has six state-of the-art PET scanners and a long history of performing PET scanning in neurological disorders, and in animal models thereof (www.turkupetcentre.fi). Radiochemical synthesis of 11C-PK11195 has been established in TPC and study projects on MS patients have been completed and published by our research group previously. The 11C-TMSX and 11C-UCB-J are already in use in the TPC.
People involved: Dr. Laura Airas, MD, PhD. Consultant in neurology, and assistant professor in neurology. Professor Juha Rinne, MD, Consultant in Neurology. Turku PET Centre. Professor Riitta Parkkola, MD, Neuroradiologist. Dr. Eero Rissanen MD, PhD. Dr. Marcus Sucksdorff, MD, PhD student.
- Conditions
- Multiple Sclerosis
- Medical subject headings
- Multiple Sclerosis
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| Clinical follow-up | Clinical follow-up of MS-patients for 5 years. PET imaging data with PK11195 and TMSX only in baseline and with UCB-J at 5 years | |
| Healthy controls | comparison of healthy controls' and MS patients' PET imaging data with PK11195 and TMSX only in baseline and with UCB-J at 5 years |
What is being measured
The primary outcome is the main question the study is designed to answer.
Correlation of microglial activation and MS progression
11C-PK11195-radioligand binding using PET
Measured: 5 years
Secondary outcomes (2)
Correlation of 11C-TMSX radioligand binding and MS progression
11C-TMSX-radioligand binding using PET
Measured: 5 years
Correlation of 11C-UCB-J-radioligand binding and cognition
Correlation 11C-UCB-J-radioligand binding and cognitive function
Measured: 5 years
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted1 May 2017
- Study startApr 2016
- Primary completionDec 2023
- Study completionDec 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (2)Papers the sponsor has linked to this study.
- Other trials for Multiple SclerosisStudies of the same condition, open and under way.
- More trials run by Turku University HospitalThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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
- Time perspective
- Prospective
- Enrolment
- 35 participants (actual)
Sponsor and investigators
- Lead sponsor
- Turku University Hospital
- Sponsor type
- Other government
- Responsible party
- Sponsor
- Investigators
- Laura Airas, MD, Docent, Principal investigator, Turku University Hospital, division of clinical neurosciences
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT03134716
- Sponsor's protocol ID
- T99/2016
- Acronym
- PROMS
- Status last verified
- Sep 2025
- First submitted
- 14 Apr 2016
- Last updated
- 22 Sep 2025
- Results posted
- No
- Data monitoring committee
- No
- Individual data sharing
- Undecided: Multi-center collaboration under discussion
Publications
Laaksonen S, Sucksdorff M, Vuorimaa A, Kuhle J, Nylund M, Rajander J, Wahlroos S, Matilainen M, Saraste M, Airas L. Predictors of risk of secondary progression in multiple sclerosis. Ther Adv Neurol Disord. 2025 Sep 9;18:17562864251357276. doi: 10.1177/17562864251357276. eCollection 2025.
PubMed 40951543Sjoros T, Saraste M, Matilainen M, Nylund M, Koivumaki M, Kuhle J, Leppert D, Airas L. Serum glial fibrillary acid protein associates with TSPO-expressing lesions in multiple sclerosis brain. Ther Adv Neurol Disord. 2025 Jul 28;18:17562864251352998. doi: 10.1177/17562864251352998. eCollection 2025.
PubMed 40756531
Study at a glance
From the registry record, last updated by the sponsor on 22 Sep 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Role of Microglia in the Pathogenesis of Progressive Multiple Sclerosis
- ClinicalTrials.gov ID
- NCT03134716
- Acronym / sponsor ID
- PROMS / T99/2016
- Conditions
- Multiple Sclerosis
- Study type
- Observational
- Recruitment status
- Active, not recruiting
- Enrolment
- 35 participants (actual)
- Lead sponsor
- Turku University HospitalOther government
- Study start
- Apr 2016
- Primary completion
- Dec 2023 (actual)
- Study completion
- Dec 2026 (estimated)
- First posted
- 1 May 2017 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Our aim is to evaluate whether translocator binding protein (TSPO)-imaging correlates to Expanded Disability Status Scale (EDSS) and other disease progression-related clinical and paraclinical parameters in a homogenous cohort of 40-50-year old MS-patients, who are at risk of progression. The A2A-AR expression in this cohort will also be studied using the adenosine A2A-receptor (A2A-AR)-binding radioligand 11C-TMSX. The study cohort will also form the basis for a later follow-up study, which will be performed to evaluate the prognostic value of baseline TSPO-imaging in terms of disease progression. TSPO-imaging could thus be used as an imaging biomarker to help identifying patients to therapeutically prevent progression of MS. At the 5 year time point synaptic density will be evaluated using 11C-UCB-J radioligand and PET imaging.
Detailed description
Protocol title: Role of microglia in the pathogenesis of progressive multiple sclerosis
Rationale of the study: The investigators have demonstrated earlier a statistically significant correlation between TSPO-binding and EDSS in a heterogeneous MS-population comprising both early RRMS and late secondary progressive multiple sclerosis (SPMS) patients. Now the investigators aim to evaluate whether TSPO-imaging correlates to EDSS and other disease progression-related clinical and paraclinical parameters in a homogenous cohort of 40-50-year old MS-patients, who are at risk of progression. The A2A-AR expression in this cohort will also be studied using the A2A-AR-binding radioligand 11C-TMSX. The study cohort will also form the basis for a later follow-up study, which will be performed to evaluate the prognostic value of baseline TSPO-imaging in terms of disease progression. TSPO-imaging could thus be used as an imaging biomarker to help identifying patients to therapeutically prevent progression of MS. At the 5 year time point synaptic density will be evaluated using 11C-UCB-J radioligand and PET imaging.
Study population: The study population will consist of a clinically homogenous group of 25 relapsing remitting multiple sclerosis (RRMS) patients with MS-diagnosis for at least 5 years, age 40-50 years, who may be using any first-line MS therapy. The patients will be recruited from the outpatient clinic of the Division of Clinical Neurosciences of the University Hospital of Turku, Finland. In addition the investigators will image a group of 10 age- and sex-matched healthy control subjects for comparison.
Study Objectives Primary: To evaluate how TSPO-ligand binding in the normal appearing white matter (NAWM) correlates to EDSS.
Secondary: 1) To evaluate how TSPO-ligand binding in the NAWM at baseline correlates to other standard clinical and paraclinical parameters typically associated with disease progression 2) To evaluate how 11C-TMSX-binding (to A2A-AR) correlates to the clinical and paraclinical parameters, and to TSPO-binding. 3) To evaluate how synaptic density evaluated using 11C-UCB-J binding correlates to patients cognitive functions.
Inclusion criteria: RRMS, age 40-50 years, MS-diagnosis for a minimum of five years. Exclusion criteria: Previous or present treatment with immunosuppressive medication or biologicals. Steroid treatment within 30 days of evaluation Evaluation of patients: Baseline brain MRI and PET using 11C-PK11195 and 11C-TMSX with a protocol used in our previous studies. MS functional composite (MSFC), brain atrophy, quantitative diffusion tensor magnetic resonance imaging (DTI-MRI) measures, and neuropsychological status. At 5 years PET using 11C-UCB-J radioligand.
Positron emission tomography (PET) imaging methods: 1) Detection of microglial activation. The investigators shall use the TSPO-ligand 11C-PK11195 to evaluate the level of microglial activation in the NAWM, in normal appearing gray matter (NAGM) and in the periplaque areas. The 11C-PK11195 imaging. 2) A2A-AR detection. The investigators shall investigate the distribution of the A2A-ARs using PET and (11C-TMSX). This will be performed to correlate A2A-AR expression with microglial activation in the central nervous system (CNS) of RRMS patients at risk of converting to SPMS. The 11C-TMSX imaging.3) Evaluation of synaptic density using 11C-UCB-J-PET. The association between 11C-UCB-J binding and cognitive functions will be evaluated.
Based on earlier experience with PET ligands it is estimated that 15 subjects per group is enough to reveal 15% difference in 11C-PK11195 and 11C-TMSX uptake between the study groups with 90% power at p-level <0.05. The correlation analyses between the variables will be performed with Spearman's non-parametric test for non-linear, and Pearson's test for linear association.
Facilities: Turku PET Centre (TPC) is the national PET Centre in Finland. It has six state-of the-art PET scanners and a long history of performing PET scanning in neurological disorders, and in animal models thereof (www.turkupetcentre.fi). Radiochemical synthesis of 11C-PK11195 has been established in TPC and study projects on MS patients have been completed and published by our research group previously. The 11C-TMSX and 11C-UCB-J are already in use in the TPC.
People involved: Dr. Laura Airas, MD, PhD. Consultant in neurology, and assistant professor in neurology. Professor Juha Rinne, MD, Consultant in Neurology. Turku PET Centre. Professor Riitta Parkkola, MD, Neuroradiologist. Dr. Eero Rissanen MD, PhD. Dr. Marcus Sucksdorff, MD, PhD student.
Study design
- Observational model
- Case-control
- Time perspective
- Prospective
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Clinical follow-up | – | –Clinical follow-up of MS-patients for 5 years. PET imaging data with PK11195 and TMSX only in baseline and with UCB-J at 5 years |
| Healthy controls | – | –comparison of healthy controls' and MS patients' PET imaging data with PK11195 and TMSX only in baseline and with UCB-J at 5 years |
Who may qualify
- Ages
- 40 to 50 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult
- Study population
- Relapsing remitting MS (RRMS) patients on the verge of secondary progression, age 40-50 years, MS-diagnosis for a minimum of five years before entering the study.
Key inclusion criteria (1 listed)
- RRMS, age 40-50 years, MS-diagnosis for a minimum of five years.
Key exclusion criteria (1 listed)
- Previous or present treatment with immunosuppressive medication or biologicals. - Steroid treatment within 30 days of evaluation
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Correlation of microglial activation and MS progression
Time frame: 5 years
11C-PK11195-radioligand binding using PET
2 secondary outcomes
Correlation of 11C-TMSX radioligand binding and MS progression
Time frame: 5 years
Correlation of 11C-UCB-J-radioligand binding and cognition
Time frame: 5 years
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 22 Sep 2025.
- Derived from this study: PubMed 40951543Laaksonen S, Sucksdorff M, Vuorimaa A, Kuhle J, Nylund M, Rajander J, Wahlroos S, Matilainen M, Saraste M, Airas L. Predictors of risk of secondary progression in multiple sclerosis. Ther Adv Neurol Disord. 2025 Sep 9;18:17562864251357276. doi: 10.1177/17562864251357276. eCollection 2025.
- Derived from this study: PubMed 40756531Sjoros T, Saraste M, Matilainen M, Nylund M, Koivumaki M, Kuhle J, Leppert D, Airas L. Serum glial fibrillary acid protein associates with TSPO-expressing lesions in multiple sclerosis brain. Ther Adv Neurol Disord. 2025 Jul 28;18:17562864251352998. doi: 10.1177/17562864251352998. eCollection 2025.
- Individual participant dataSharing planned: Undecided. Multi-center collaboration under discussion
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Laura Airas, MD, Docent principal investigator
Turku University Hospital, division of clinical neurosciences
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Multiple Sclerosis, run by Turku University Hospital at 1 site in Finland.
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 1 inclusion and 1 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 22 Sep 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Finland. 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.
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?
Correlation of microglial activation and MS progression (time frame: 5 years). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT03134716, which also lists 2 linked publications.
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 22 Sep 2025.