Active Secondary Progressive Multiple SclerosisITASIANCT05376579
Impact of Mayzent on aSPMS Patients in a Long-term NIS in Italy
An observational study of Active Secondary Progressive Multiple Sclerosis, run by Novartis Pharmaceuticals at 24 sites in Italy.
Trial summary
This is an observational, multicenter, single-arm, prospective study conducted in Italy Read more about this study
- Who is it for?
- Ages 18 to 60 years
- Conditions the study is for
- Active Secondary Progressive Multiple Sclerosis
- What is being tested?
- siponimod
- How many people
- 134 participants
- Where
- 24 sitesItaly
- Study dates
- 17 Jun 2022to 22 Jul 2025
- 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 to 60 years
- All sexes
- No healthy volunteers
- Adult
Study population: patients in Italy with active SPMS treated with siponimod as per label and local clinical practice.
Who may be able to join
- Signed informed consent: patient must provide written informed consent before any study assessment is performed.
- Male/female participants aged between 18 and 60.
- Documented diagnosis of active SPMS.
- Siponimod treatment as routine medical care: patients newly treated with siponimod (starting not more than 7 days before baseline visit), for whom the decision to start treatment has already been taken independently of study inclusion based on clinical practice and according to SmPC and AIFA criteria, and who successfully qualified for treatment with siponimod (i.e. passed the screening procedure mandated by the SmPC and Risk Management Plan (RMP) for this treatment, including genotyping for CYP2C9 to determine CYP2C9 metaboliser status).
Who cannot join
- Patients treated outside the approved siponimod label or with any controindication indicated in the SmPC.
- Pregnant or lactating women.
- Patients with any clinical condition that may interfere with the subject's ability to cooperate and comply with the study procedures based on the investigator's judgement.
- Current participation in an interventional trial.
- Treatment with siponimod prior to inclusion in this study (siponimod can be started not more than 7 days before baseline visit).
Trial locations and contacts
24 sites in 1 country.
24 sites in 1 country
Italy24 sites
Novartis Investigative Site
Ancona, AN, 60126
Novartis Investigative Site
Bergamo, BG, 24127
Novartis Investigative Site
Bologna, BO, 40124
Novartis Investigative Site
Brescia, BS, 25123
Novartis Investigative Site
Catanzaro, CZ, 88100
Novartis Investigative Site
Como, CO, 22100
Novartis Investigative Site
Foggia, FG, 71122
Novartis Investigative Site
Genova, GE, 16132
Novartis Investigative Site
L’Aquila, AQ, 67100
Novartis Investigative Site
Messina, ME, 98124
Novartis Investigative Site
Milan, MI, 20133
Novartis Investigative Site
Naples, 80131
Novartis Investigative Site
Naples, 80138
Novartis Investigative Site
Novara, 28100
Novartis Investigative Site
Orbassano, TO, 10043
Novartis Investigative Site
Padova, PD, 35128
Novartis Investigative Site
Palermo, PA, 90127
Novartis Investigative Site
Pavia, PV, 27100
Novartis Investigative Site
Pisa, PI, 56126
Novartis Investigative Site
Roma, RM, 00133
Novartis Investigative Site
Roma, RM, 00152
Novartis Investigative Site
Roma, RM, 00189
Novartis Investigative Site
Trieste, TS, 34149
Novartis Investigative Site
Vicenza, VI, 36100
About this study
Official title: Impact of Mayzent (Siponimod) on Active Secondary Progressive Multiple Sclerosis Patients in a Long-term Non-interventional Study in Italy
This is an observational, multicenter, single-arm, prospective study conducted in Italy
Read the detailed description
Primary data will be collected over a period of three years. Medical history of participants will be collected including EDSS, MRI outcomes, relapses and previous medication to allow the estimation of the effects of siponimod treatment on an individual basis.
- Being tested
- siponimod
- Keywords
- Secondary Progressive Multiple Sclerosis, aSPMS, NIS, Italy, Mayzent, siponimod
- Medical subject headings
- Multiple Sclerosis, Chronic Progressive
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
siponimodOther
Also called mayzent
Prospective observational cohort study. There is no treatment allocation. Patients will be invited to participate in the study after the independent decision by physician and patient to start siponimod treatment as routine clinical care.
| Study group | Role | What they receive |
|---|---|---|
| siponimod | patients treated with siponimod Receives: Other: siponimod |
What is being measured
The primary outcome is the main question the study is designed to answer.
Proportion of patients with six-month CDP during 36 months of treatment
Confirmed disability progression (CDP) is defined as a ≥1.0-point worsening of Expanded Disability Status Scale (EDSS) score from ≤5.0 baseline or a 0.5-point worsening from >5.0 baseline for at least 6 months OR a ≥4.0-point confirmed cognitive worsening (CCW) from baseline of Symbol Digit Modalities Test (SDMT) for at least 6 months.
Measured: 36 months
Secondary outcomes (19)
Annualized relapse rate (ARR)
ARR is the number of relapses during the period / person-years of subject Person-years for subject = period (in days) / 365.25
Measured: Month 12, month 24 and month 36
Number of new/newly enlarging T2 [neT2] and Gd+T1 lesions
Number of new/newly enlarging T2-hyperintense lesions and number of new 1 gadolinium-enhancing (Gd+) lesions is collected
Measured: Baseline, month 3, month 6, month 12, month 18, month 24, month 30 and month 36
Expanded Disability Status Scale scores
Expanded Disability Status Scale (EDSS) score is composed of the overall impression and individual scores of the following functional systems: cognition, mood, fatigue, vision, brain stem, upper extremities, lower extremities, bladder-intestinal function, sexuality. Scores are on a scale of 0 (healthy) to 10 (death from MS) with 0.5 unit increments
Measured: Month 12, month 24 and month 36
Expanded Disability Status Scale trend
EDSS trend is measured by differentiating patients who stabilize from those who experience an increase of EDSS score (increment of ≥1 or ≥0.5 point if baseline EDSS was ≤5.0 or ˃5.0, respectively). Moreover, patients with progression will be categorized as patients with continuous disability accrual (CDA) or one-step worsening (OneS-wors), defined as:
- OneS-wors: the occurrence of one single episode of confirmed EDSS deterioration.
- CDA: occurrence of at least two episodes of OneS-wors associated with continuous disability progression between at least two time points.
Measured: Month 12, month 24 and month 36
Proportion of patients with No Evidence of Disease Activity (NEDA)-3
NEDA-3 is defined as no Confirmed disability progression (CDP), no confirmed relapse and absence of T1 gadolinium-enhancing (Gd+) lesions.
Measured: Month 12, month 24 and month 36
UK Neurological Disability Scale (UKNDS)
The UKNDS is a questionnaire for recording impairments in MS from the patient's perspective and considers 12 functional systems: perception and thinking, mood, vision, speech and communication, swallowing, arm and hand function, walking ability, bladder function, bowel function, fatigue, sexuality, pain, cramps and others. Answering the questions results in a score of 0 (no disability) to 60 (maximum disability). This questionnaire will be completed by the patients during site visits.
Measured: Baseline, month 3, month 6, month 12, month 18, month 24, month 30 and month 36
Fatigue Scale for Motor and Cognitive Functions (FSMC)
The FSMC is a patient questionnaire for the clarification of cognitive and motor fatigue, a typical symptom of MS (Penner et al., 2009), and considers a cognitive, motor and total score. Score ranges from 200 to 100, the greater the score the greater the impairment caused by fatigue.
Measured: Baseline, month 3, month 6, month 12, month 18, month 24, month 30 and month 36
Hospital Anxiety and Depression Scale (HADS)
The HADS has seven items each for depression and anxiety subscales. Scoring for each item ranges from zero to three, with three denoting highest anxiety or depression level. A total subscale score of >8 points out of a possible 21 denotes considerable symptoms of anxiety or depression.
Calculations of scores: each of the 14 items is rated on a 4-point scale ('Yes, definitely', 'Yes, sometimes', 'No, not much' and 'No, not at all'). All items except 7 and 10 are scored as 'Yes, definitely' = 3 to 'No, not at all' = 0. Items 7 and 10 are scored as 'Yes, definitely' = 0 to 'No, not at all' = 3. The HADS consists of two sub-scores: the HAD-A for anxiety and HAD-D for depression; each sub-score ranges from 0 to 21 points; scores ≥11 indicate the presence of anxious or depressive disorders; scores between 8-10 points are borderline abnormal, and scores of ≤7 indicate that the disorder is not present.
Measured: Baseline, month 3, month 6, month 12, month 18, month 24, month 30 and month 36
Symbol Digit Modality test (SDMT)
The SDMT is a sensitive and specific test to investigate attention, concentration and information processing speed, which are typically impaired in cognitively impaired MS patients.
Nine numbers are shown paired with 9 corresponding individual symbols. Below this are further lines with symbols and empty boxes. The patients must assign the correct numbers to the symbols as quickly as possible. The number of correctly assigned numbers within 90 seconds gives the test score. The total duration of the test is about 5 minutes and scores range between 0 and 110 where higher scores indicate better result.
A deterioration of the SDMT score by ≥4 points is considered clinically relevant
Measured: Baseline, month 3, month 6, month 12, month 18, month 24, month 30 and month 36
Clinical Global Impression (CGI)
The CGI scale represents a short, independent assessment by the treating physician of the overall condition of the patient.
It incorporates patient history, psychosocial circumstances, symptoms, behavior and the influence of symptoms on the patient's functional ability. The CGI consists of three different global measures and all three will be evaluated: Severity of illness (CGI-S) ranges from 0 to 7, Global Improvement (CGI-I) ranges from 0 to 7 and Efficacy index (CGI-E) ranges from 0 to 16. A higher score means a severe impact on the disease.
Measured: Baseline, month 3, month 6, month 12, month 18, month 24, month 30 and month 36
MS activity status (MS-AS) - number of relapse
Number of relapse, number of relapse that affects the daily activities, number of relapse that required an hospitalization and number of treated relapse to be collected
Measured: Baseline, month 3, month 6, month 12, month 18, month 24, month 30 and month 36
MS activity status (MS-AS) - Number of patients with presence of symptoms
Number of patients with presence of symptoms to be collected
Measured: Baseline, month 3, month 6, month 12, month 18, month 24, month 30 and month 36
T25-foot-walk
The T25-FW is an objective and quantitative test of the lower extremities. The time in seconds it takes a patient to walk a distance of 25 feet (7.62 m) is measured. The patient should walk as quickly and safely as possible. This test is performed twice in a row and the mean value of the time required is documented in seconds. An improvement or deterioration of 20% is considered a significant change
Measured: Baseline, month 3, month 6, month 12, month 18, month 24, month 30 and month 36
9-Hole peg test
This test examines manual dexterity. Patients must individually remove nine pegs from a flat dish with one hand and insert them into corresponding holes in a test board. The pegs are then placed back into the dish with the same hand. Two rounds are performed per hand and the average value of the time required is documented in seconds
Measured: Baseline, month 3, month 6, month 12, month 18, month 24, month 30 and month 36
EQ-5D: EuroQol five-dimensional
The EQ-5D is a generic multidimensional measurement tool for describing health-related quality of life (EuroQol, 1999). The five domains of mobility, self-care ability, daily activities, pain/discomfort and anxiety/depression are considered. For each of the dimensions, the most appropriate answer from three given possibilities is selected (1=no problem, 2=moderate problem, 3=large problem). In addition, the patient marks the current state of health on a scale from 0 (worst conceivable state of health) to 100 (best conceivable state of health).
Measured: Baseline, month 3, month 6, month 12, month 18, month 24, month 30 and month 36
TSQM-9: Treatment Satisfaction Questionnaire for Medication
The TSQM-9 is a questionnaire to assess patient satisfaction with siponimod treatment. The TSQM-9 is a sound and valid measure of the major dimensions of patients' satisfaction with medication and also a good predictor of adherence across different types of medication and patient population.
Effectiveness, side effects, simplicity and overall satisfaction are all rated between 0 and 100. Higher values mean a worse condition. Responses to items are summed and transformed so that higher scores indicate greater satisfaction. Specifically, TSQM-9 scale scores are computed by adding the items loading on each domain. The lowest possible score is subtracted from the composite score and divided by the greatest possible score range. This provides a transformed score between 0 and 1 that is then multiplied by 100. If more than one item is missing from a subscale of the TSQM-9 for a particular patient, this subscale should be considered invalid for that respondent.
Measured: Baseline, month 3, month 6, month 12, month 18, month 24, month 30 and month 36
Exposure adjusted proportion of patients with adverse event (AE) or serious adverse event (SAE) per 100 subject-years
Exposure adjusted proportion of patients with adverse event (AE) or serious adverse event (SAE) per 100 subject-years to be collected
Measured: Up to 36 months
Discontinuation rates due to AE or other reasons
Discontinuation rates due to AE or other reasons to be collected
Measured: Up to 36 months
Proportion of patient who required FDO when starting siponimod and the reason why
Proportion of patient who required first dose observation (FDO) when starting siponimod and the reason why
Measured: Baseline
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted17 May 2022
- Study start17 Jun 2022
- Primary completion22 Jul 2025
- Study completion22 Jul 2025
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Active Secondary Progressive Multiple SclerosisStudies of the same condition, open and under way.
- More trials run by Novartis PharmaceuticalsThe 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
- Cohort
- Time perspective
- Prospective
- Enrolment
- 134 participants (actual)
Sponsor and investigators
- Lead sponsor
- Novartis Pharmaceuticals
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- Novartis Pharmaceuticals, Study director, Novartis Pharmaceuticals
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05376579
- Sponsor's protocol ID
- CBAF312AIT04
- Acronym
- ITASIA
- Status last verified
- Dec 2025
- First submitted
- 12 May 2022
- Last updated
- 19 May 2026
- Results posted
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 19 May 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Impact of Mayzent (Siponimod) on Active Secondary Progressive Multiple Sclerosis Patients in a Long-term Non-interventional Study in Italy
- ClinicalTrials.gov ID
- NCT05376579
- Acronym / sponsor ID
- ITASIA / CBAF312AIT04
- Keywords
- Secondary Progressive Multiple Sclerosis, aSPMS, NIS, Italy, Mayzent, siponimod
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 134 participants (actual)
- Lead sponsor
- Novartis PharmaceuticalsIndustry (pharma, biotech, devices)
- Study start
- 17 Jun 2022 (actual)
- Primary completion
- 22 Jul 2025 (actual)
- Study completion
- 22 Jul 2025 (actual)
- First posted
- 17 May 2022 (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.
This is an observational, multicenter, single-arm, prospective study conducted in Italy
Detailed description
Primary data will be collected over a period of three years. Medical history of participants will be collected including EDSS, MRI outcomes, relapses and previous medication to allow the estimation of the effects of siponimod treatment on an individual basis.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| siponimod | – | Other: siponimodpatients treated with siponimod |
Who may qualify
- Ages
- 18 to 60 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult
- Study population
- patients in Italy with active SPMS treated with siponimod as per label and local clinical practice.
Key inclusion criteria (4 listed)
- Signed informed consent: patient must provide written informed consent before any study assessment is performed.
- Male/female participants aged between 18 and 60.
- Documented diagnosis of active SPMS.
- Siponimod treatment as routine medical care: patients newly treated with siponimod (starting not more than 7 days before baseline visit), for whom the decision to start treatment has already been taken independently of study inclusion based on clinical practice and according to SmPC and AIFA criteria, and who successfully qualified for treatment with siponimod (i.e. passed the screening procedure mandated by the SmPC and Risk Management Plan (RMP) for this treatment, including genotyping for CYP2C9 to determine CYP2C9 metaboliser status).
Key exclusion criteria (5 listed)
- Patients treated outside the approved siponimod label or with any controindication indicated in the SmPC.
- Pregnant or lactating women.
- Patients with any clinical condition that may interfere with the subject's ability to cooperate and comply with the study procedures based on the investigator's judgement.
- Current participation in an interventional trial.
- Treatment with siponimod prior to inclusion in this study (siponimod can be started not more than 7 days before baseline visit).
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| siponimodAlso: mayzentProspective observational cohort study. There is no treatment allocation. Patients will be invited to participate in the study after the independent decision by physician and patient to start siponimod treatment as routine clinical care. | Other | siponimod |
Primary outcome
Proportion of patients with six-month CDP during 36 months of treatment
Time frame: 36 months
Confirmed disability progression (CDP) is defined as a ≥1.0-point worsening of Expanded Disability Status Scale (EDSS) score from ≤5.0 baseline or a 0.5-point worsening from >5.0 baseline for at least 6 months OR a ≥4.0-point confirmed cognitive worsening (CCW) from baseline of Symbol Digit Modalities Test (SDMT) for at least 6 months.
19 secondary outcomes
Annualized relapse rate (ARR)
Time frame: Month 12, month 24 and month 36
Number of new/newly enlarging T2 [neT2] and Gd+T1 lesions
Time frame: Baseline, month 3, month 6, month 12, month 18, month 24, month 30 and month 36
Expanded Disability Status Scale scores
Time frame: Month 12, month 24 and month 36
Expanded Disability Status Scale trend
Time frame: Month 12, month 24 and month 36
Proportion of patients with No Evidence of Disease Activity (NEDA)-3
Time frame: Month 12, month 24 and month 36
UK Neurological Disability Scale (UKNDS)
Time frame: Baseline, month 3, month 6, month 12, month 18, month 24, month 30 and month 36
Fatigue Scale for Motor and Cognitive Functions (FSMC)
Time frame: Baseline, month 3, month 6, month 12, month 18, month 24, month 30 and month 36
Hospital Anxiety and Depression Scale (HADS)
Time frame: Baseline, month 3, month 6, month 12, month 18, month 24, month 30 and month 36
Symbol Digit Modality test (SDMT)
Time frame: Baseline, month 3, month 6, month 12, month 18, month 24, month 30 and month 36
Clinical Global Impression (CGI)
Time frame: Baseline, month 3, month 6, month 12, month 18, month 24, month 30 and month 36
MS activity status (MS-AS) - number of relapse
Time frame: Baseline, month 3, month 6, month 12, month 18, month 24, month 30 and month 36
MS activity status (MS-AS) - Number of patients with presence of symptoms
Time frame: Baseline, month 3, month 6, month 12, month 18, month 24, month 30 and month 36
T25-foot-walk
Time frame: Baseline, month 3, month 6, month 12, month 18, month 24, month 30 and month 36
9-Hole peg test
Time frame: Baseline, month 3, month 6, month 12, month 18, month 24, month 30 and month 36
EQ-5D: EuroQol five-dimensional
Time frame: Baseline, month 3, month 6, month 12, month 18, month 24, month 30 and month 36
TSQM-9: Treatment Satisfaction Questionnaire for Medication
Time frame: Baseline, month 3, month 6, month 12, month 18, month 24, month 30 and month 36
Exposure adjusted proportion of patients with adverse event (AE) or serious adverse event (SAE) per 100 subject-years
Time frame: Up to 36 months
Discontinuation rates due to AE or other reasons
Time frame: Up to 36 months
Proportion of patient who required FDO when starting siponimod and the reason why
Time frame: Baseline
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 19 May 2026.
- Link to study resultsLink provided by the sponsor.
- Individual participant dataSharing planned: No
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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.
Novartis Pharmaceuticals study director
Novartis Pharmaceuticals
24 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Active Secondary Progressive Multiple Sclerosis, run by Novartis Pharmaceuticals at 24 sites in Italy.
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 4 inclusion and 5 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 19 May 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 24 sites in Italy. 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?
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?
Proportion of patients with six-month CDP during 36 months of treatment (time frame: 36 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 19 May 2026.