AzTrials
AzTrials

Multiple SclerosisORIONNCT07898371

A Study to Describe Multiple Sclerosis Patients Treated With Tolebrutinib as Per Label in a Real-world Setting

An observational study of Multiple Sclerosis, run by Sanofi at 1 site in United Arab Emirates.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
Search all trials

Trial summary

This study aims to assess the real-world treatment patterns, data from patient reported outcomes, the effectiveness profile of tolebrutinib, and health care utilization data in routine practice. The decision to initiate tolebrutinib treatment is made by the treating neurologist as part of standard of care. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Multiple Sclerosis
What is being tested?
Tolebrutinib
How many people
3,000 participants
Where
1 siteUnited Arab Emirates
Study dates
1 Oct 2026to 1 Oct 2031
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 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: MS patients aged more than 18 years who are planned to start treatment with tolebrutinib treatment according to the approved local label. The decision to initiate tolebrutinib treatment is made by the treating neurologist as part of standard of care. Consideration and option of participation in the study will only be done once the treatment decision has been made, independent of study participation. Only upon signing the informed consent form (ICF) will the patient be enrolled in the study.

Who may be able to join

  • Willing to participate with the ability to consent and sign an Informed Consent Form (ICF).
  • Treatment decision according to approved local label. Retrospective inclusion of patients who had initiated tolebrutinib up to a maximum of 4 weeks prior to signing the ICF is allowed.

Who cannot join

  • Participation in tolebrutinib long-term safety (LTS) study or any prior tolebrutinib study; experience with any other Bruton's Tyrosine Kinase (BTK) inhibitors.
  • Current or planned/pending participation in a clinical study.
  • Inability to comply with the study protocol
  • The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Trial Transparency email recommended (Toll free for US & Canada) contact

800-633-1610 ext. option 6

Contact-US@sanofi.com

United Arab Emirates1 site, 1 recruiting
  • Harley Street Medical Centre

    Marina, Abu Dhabi Emirate

    Recruiting

Other trials in United Arab Emirates

About this study

Official title: A Multinational, Prospective, Observational Study to Describe Multiple Sclerosis (MS) Patients Treated With Tolebrutinib as Per Approved Local Label in a Real-world Setting

This study aims to assess the real-world treatment patterns, data from patient reported outcomes, the effectiveness profile of tolebrutinib, and health care utilization data in routine practice. The decision to initiate tolebrutinib treatment is made by the treating neurologist as part of standard of care. Consideration and option of participation in the study will only be done once the treatment decision has been made, independent of study participation. Only upon signing the informed consent form (ICF) will the patient be enrolled in the study. The patient's participation in the study will not influence the MS treatment. Total study duration of study is 5 years per country comprising an approximately 24-months of enrollment period followed by a 36-month individual observational period.

Being tested
Tolebrutinib
Medical subject headings
Multiple Sclerosis

What participants receive

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

  • TolebrutinibDrug

    This study will not administer any treatment, only observe the treatment as prescribed in real-world clinical practice.

Study groups in NCT07898371
Study groupRoleWhat they receive
TolebrutinibNot described
Receives: Drug: Tolebrutinib

What is being measured

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

  1. Socio-demographic Characteristics

    Number and percentage of participants with socio-demographic characteristics including age, gender, occupational status will be collected.

    Measured: Baseline

  2. Disease History: Most Recent Disability Status Scale (EDSS) score

    Disease history including EDSS score will be collected. The EDSS is a clinician-rated scale, ranging from 0 (normal neurological status) and 10 (death due to MS). Patients with EDSS score up to 4.5 are fully ambulant. Up to this point, the main determinant of EDSS are functional systems (FS), the ambulation status is the main determinant in the degree of disability after 4.5.

    Measured: Baseline

  3. Disease History: EDSS Progression in Past 12 Months

    Disease history including EDSS progression in past 12 Months will be collected. The EDSS is a clinician-rated scale, ranging from 0 (normal neurological status) and 10 (death due to MS). Patients with EDSS score up to 4.5 are fully ambulant. Up to this point, the main determinant of EDSS are functional systems (FS), the ambulation status is the main determinant in the degree of disability after 4.5.

    Measured: Baseline

  4. Disease History: Time Since Relapsing-Remitting Multiple Sclerosis (RRMS) Symptom Onset

    Disease history including time (in years) since RRMS symptom onset will be collected.

    Measured: Baseline

  5. Disease History: Time Since Secondary Progressive Multiple Sclerosis (SPMS) Diagnosis

    Disease history including time (in years) since SPMS diagnosis will be collected.

    Measured: Baseline

  6. Disease History: Time Since Most Recent Clinical Relapse

    Disease history including time (in years) since most recent clinical relapse will be collected.

    Measured: Baseline

  7. Disease History: Number and Type of Previous MS Treatments

    Disease history including number and type of previous MS treatments will be collected.

    Measured: Baseline

  8. Disease History: Number and Type of Prior and Current Disease Modifying Therapies (DMTs)

    Disease history including number and type prior and current DMTs will be collected.

    Measured: Baseline

  9. Disease History: Number of Participants with Comorbidities

    Disease history including comorbidities will be collected.

    Measured: Baseline

  10. Disease History: Number of Participants with Medical History

    Disease history including medical history will be collected.

    Measured: Baseline

  11. Disease History: Number of Participants with Concomitant Medication

    Disease history including concomitant medication will be collected.

    Measured: Baseline

  12. Magnetic Resonance Imaging Data

    MRI data will be collected.

    Measured: Baseline

Secondary outcomes (17)
  1. Change from Baseline in Individual Expanded Disability Status Scale (EDSS) Score

    The EDSS is a clinician-rated scale, ranging from 0 (normal neurological status) and 10 (death due to MS). Patients with EDSS score up to 4.5 are fully ambulant. Up to this point, the main determinant of EDSS are functional systems (FS), the ambulation status is the main determinant in the degree of disability after 4.5.

    Measured: Baseline up to 36 months

  2. Change from Baseline in Timed 25-Foot Walk Test (T25FW)

    The mean walk time will be used for assessment of the patient's walking ability. An increase of more than 20 percent (%) from the baseline in the T25-FW test is considered meaningful worsening.

    Measured: Baseline up to 36 months

  3. Change from Baseline in 9-Hole Peg Test (9-HPT)

    Time to complete the 9-HPT will be used to assess a participant's manual dexterity and fine motor skills. The mean time to test completion will serve for assessment of the patient's hand dexterity. An increase of more than 20 percent (%) from the baseline in the 9-HPT is considered meaningful worsening.

    Measured: Baseline up to 36 months

  4. Change from Baseline in Symbol Digit Modalities Test (SDMT)

    The SDMT is used to assess visual scanning, tracking and motor speed, and has been designed to detect cognitive impairment. The SDMT involves a simple substitution task that normal children and adults can easily perform. Using a reference key, the examinee has 90 seconds to pair specific numbers with given geometric figures.

    Measured: Baseline up to 36 months

  5. Change from Baseline in Multiple Sclerosis Impact Scale-29 (MSIS-29)

    The MSIS-29 is a scale that measures the physical (20 items) and psychological (9 items) impact of MS. Two summary scores (eg, the physical scale and the psychological scale) are calculated by summing up individual items in each scale and transforming the scores into a 0-100 scale. High scores indicate a higher impact of MS on the patient's physical and/or psychological health.

    Measured: Baseline up to 36 months

  6. Change from Baseline in Short Form Health Survey (SF-36) The

    The SF-36 is a 36-item questionnaire designed to measure health-related quality of life. It assesses eight domains of health, including physical functioning, bodily pain, general health perceptions, vitality, social functioning, role limitations due to physical health problems, role limitations due to emotional problems, and mental health.

    Measured: Baseline up to 36 months

  7. Change from Baseline in Multiple Sclerosis International Quality of Life (MuSIQoL)

    The MusiQoL questionnaire is a 31-item, MS-specific tool that measures quality of life from the patient's perspective. It covers nine domains-daily activities, psychological well-being, symptoms, relationships with friends and family, sentimental/sexual life, coping, and experiences of rejection-plus an overall index score. Items use a five-point scale, with higher scores reflecting better quality of life.

    Measured: Baseline up to 36 months

  8. Change from Baseline in Multiple Sclerosis Walking Scale (MSWS-12)

    The 12-item MSWS is a validated patient-reported measure of the impact of MS on the individual's walking ability. A low MSWS-12 score indicates minimal impact of MS on walking ability, reflecting better mobility and fewer limitations in daily activities. Conversely, a high MSWS-12 score indicates a greater impact of MS on walking reflecting more significant mobility impairment and increased difficulty performing walking-related tasks.

    Measured: Baseline up to 36 months

  9. Change from Baseline in Modified Fatigue Impact Scale (MFIS)

    The MFIS, 21-item questionnaire, is designed to evaluate how fatigue affects physical, cognitive, and psychosocial functioning. A lower MFIS score indicates that fatigue has minimal impact on a person's physical, cognitive, and psychosocial functioning. In contrast, a higher MFIS score reflects a greater impact of fatigue, suggesting more substantial interference with daily activities and overall quality of life.

    Measured: Baseline up to 36 months

  10. Change from Baseline in Fatigue Scale for Motor and Cognitive Functions (FSMC)

    The FSMC is a 20-item questionnaire designed to assess both cognitive and motor fatigue, particularly in individuals with MS. Each item is rated on a 5-point Likert scale, ranging from "does not apply at all" to "applies completely," resulting in a total score between 20 (no fatigue) and 100 (severe fatigue).

    Measured: Baseline up to 36 months

  11. Change from Baseline in Treatment Satisfaction Questionnaire for Medication (TSQM)

    The 14-item TSQM is a tool to assess patient satisfaction with medication. The tool includes four domains: Effectiveness (3 items), Side Effects (5 items), Convenience (3 items), and Global Satisfaction (3 items). It uses 5- or 7-point Likert-type scales and Yes/No responses.

    Measured: Baseline up to 36 months

  12. Change from Baseline in Work Productivity and Activity Impairment - Multiple Sclerosis (WPAI-MS)

    The WPAI-MS questionnaire is a 6-item instrument to measure impairments over the past 7 days in both paid work and unpaid work due to one's health. Respondents are asked questions about work and activity impairment due to health problems.

    Measured: Baseline up to 36 months

  13. Change from Baseline in Chronic Treatment Acceptance Questionnaire (ACCEPT)

    The ACCEPT is a patient questionnaire with 25 items which evaluates the patient's acceptance of long-term treatment in real-life. Low scores indicate poor acceptance, moderate scores reflect a neutral stance, and high scores indicate strong acceptance.

    Measured: Baseline up to 36 months

  14. Change from Baseline in Patient Global Impression of Change (PGIC)

    The PGIC scale is administered at the end of the test-retest period and asks respondents to rate their symptom severity now/today compared to the beginning of the test-retest period. PGIC response options typically use a bi-directional response scale, eg, 5 to 7 options ranging from "Much better" to "Much worse" with "No change" at the midpoint. Lower scores indicate improvement, 4 indicates no change, and higher scores indicate worsening of the patient's condition.

    Measured: Baseline up to 36 months

  15. Change from Baseline in Patient Global Impression of Severity (PGIS)

    The PGIS Scale asks respondents to rate their symptom or disease severity at a given time, and it is administered at multiple timepoints, including the beginning and the end of the test-retest period. Response options, in the form of a unidirectional verbal rating scale (VRS), often range from "None" to "Very severe". Lower scores indicate mild or no symptoms, moderate scores indicate noticeable impact, and higher scores indicate severe or very severe symptoms.

    Measured: Baseline up to 36 months

  16. Change from Baseline in Health resource utilization questionnaire (HRUQ)

    The HRUQ is a PRO designed to capture patient-reported data on healthcare resource use, medication adherence, and work productivity over the past month, specifically in the context of MS management. Data collected from the HRUQ can be used to estimate healthcare utilization patterns, economic burden, and cost outcomes.

    Measured: Baseline up to 36 months

  17. Number of Participants with at Least one AE, SAE, AEs by Maximum Severity, AEs Leading to treatment Discontinuation and AESI

    An adverse event (AE) was defined as any untoward medical occurrence in a subject who received study drug and did not necessarily had a causal relationship with the study treatment. Serious AEs (SAEs): Any untoward medical occurrence that resulted in any of the following outcomes: death, life-threatening, required initial or prolonged in-patient hospitalisation, persistent or significant disability/incapacity, congenital anomaly/birth defect, or considered as medically important event. An adverse event of special interest (AESI) is an adverse event (serious or non-serious) of scientific and medical concern specific to the product, for which ongoing monitoring and rapid communication to the provider is required.

    Measured: Baseline up to 36 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted27 Oct 2026
  2. Study start1 Oct 2026
  3. Primary completion21 Sep 2031 (estimated)
  4. Study completion1 Oct 2031 (estimated)

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
Cohort
Time perspective
Prospective
Enrolment
3,000 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07898371
Sponsor's protocol ID
OBS19154
Other IDs
U1111-1319-0028
Acronym
ORION
Status last verified
Oct 2026
First submitted
2 Oct 2026
Last updated
27 Oct 2026
Results posted
No
Data monitoring committee
No
Individual data sharing
Yes: Qualified researchers may request access to patient level data and related study documents including the clinical study report, study protocol with any amendments, blank case report form, statistical analysis plan, and dataset specifications. Patient level data will be anonymized and study documents will be redacted to protect the privacy of trial participants. Further details on Sanofi's data sharing criteria, eligible studies, and process for requesting access can be found at: https://vivli.org

Questions about this trial

What is this clinical trial studying?

An observational study of Multiple Sclerosis, run by Sanofi at 1 site in United Arab Emirates.

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 2 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: looking for participants now, as of the sponsor's last update on 27 Oct 2026. 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 United Arab Emirates. 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?

Contact Trial Transparency email recommended (Toll free for US & Canada) (800-633-1610 ext. option 6, Contact-US@sanofi.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Socio-demographic Characteristics (time frame: Baseline). The study lists 12 primary outcomes in all. 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 27 Oct 2026.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in