Multiple Sclerosis, Relapsing-RemittingTEC-ADHERENCT04221191
Dimethyl Fumarate (DMF, Tecfidera®) Persistence in RR-MS Patients Included in the French Patient Support Program OroSEP
An observational study of Multiple Sclerosis, Relapsing-Remitting, run by Biogen at 63 sites in France.
Trial summary
The primary objective is to compare oral dimethyl fumarate (DMF) persistence at six months in relapsing-remitting multiple sclerosis (RR-MS) participants initiating DMF with and without OroSEP patient support program (PSP), respectively. Read more about this study
- Who is it for?
- Ages 18 to 55 years
- Conditions the study is for
- Multiple Sclerosis, Relapsing-Remitting
- What is being tested?
- Dimethyl Fumarate and PSP
- How many people
- 353 participants
- Where
- 63 sitesFrance
- Study dates
- 19 Aug 2019to 14 Sep 2022
- 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 55 years
- All sexes
- No healthy volunteers
- Adult
Study population: Study population included participants with RR-MS treated with DMF in clinical practice.
Who may be able to join
- Ability to understand the purpose and risks of the study and giving oral informed consent regarding TEC-ADHERE study and authorization to use protected health information (PHI) in accordance with national and local participant privacy regulations;
- Diagnosis of RR-MS;
- Initiating oral DMF according to Summary of Product Characteristics (SmPC) at the inclusion visit;
- Expanded Disability Status Score (EDSS) under 6.
Who cannot join
- Participants with progressive form of Multiple Sclerosis (MS);
- With memory or psychiatric disorders preventing them to complete questionnaires in the study.
- Note: Other protocol defined Inclusion/Exclusion criteria may apply.
Trial locations and contacts
63 sites in 1 country.
63 sites in 1 country
France63 sites
Ch D'Agen
Agen, 47000
CH d'Aix-en-Provence
Aix-en-Provence, 13616
CHU Amiens
Amiens, 80000
CHU D'amiens
Amiens, 80000
Cabinet Medical
Angoulême, 16000
Cabinet Medical Neurolac
Annecy, 74960
CH Antibes
Antibes, 06600
Hopital Prive Antony
Antony, 92160
CH d'Arras
Arras, 62000
CH de Bastia
Bastia, 20600
Chic de Bayonne
Bayonne, 64100
Cabinet du Dr Imad Malkoun
Belfort, 90000
Cabinet des Drs Chanel-Soulier et Cheron
Biarritz, 64200
Hôpital Pellegrin / Service : Neurologie
Bordeaux, 33000
Polyclinique Bordeaux-Caudéran
Bordeaux, 33200
Ch de Carcassonne
Carcassonne, 11000
Cabinet des Drs Farhat et Samad
Châtellerault, 86100
Chde Cholet
Cholet, 49300
HIA Percy
Clamart, 92140
Pole de Sante Du Plateau
Clamart, 92140
Clinique Des Cedres
Cornebarrieu, 31700
Hopital Henri Mondor
Créteil, 94000
Ch General Dax
Dax, 40100
Cabinet du Dr Pierre Gras
Dijon, 21000
CHU Dijon
Dijon, 21000
Ch de Douai
Douai, 59500
CH Simone Veil d'Eaubonne
Eaubonne, 95600
Cabinet de Dr Lotfi Kort
Évreux, 27000
Polyclinique des Alpes du Sud
Gap, 05000
CHU Grenoble Alpes CS 10217
Grenoble, 38043
Cabinet médical
La Rochelle, 17000
Pôle Espace Santé 2
La Seyne-sur-Mer, 83500
Centre Hospitalier de Libourne
Libourne, 33500
Cabinet médical Montebello
Lille, 59000
Centre Hospitalier Intercommunal JURA-SUD
Lons-le-Saunier, 39016
Chi de Haute Saone
Lure, 70200
Cabinet Du Dr Neuschwander
Lyon, 69006
Hopital
Melun, 77000
CH de Montauban
Montauban, 82000
Centre Medical Odysseum
Montpellier, 34000
Hopital Gui de Chaulliac
Montpellier, 34090
Cabinet des Drs Lorenzi Pernot et Guilloton
Mornant, 69440
Clinique d'Occitanie
Muret, 31600
Chu Caremeau
Nîmes, 30900
CHU Carémeau
Nîmes, 30900
Hôpital de la Source
Orléans, 45100
Centre Cosem Miromesnil
Paris, 75008
Cabinet du Dr Radia Djebbari
Paris, 75011
Groupe Hospitalier Paris St Joseph
Paris, 75014
Cabinet Médical Monceau
Paris, 75017
Cabinet médical
Pau, 64000
Centre Hospitalier Universitaire de Poitiers
Poitiers, 86000
Chi de Cornouaille
Quimper, 29107
Cabinet des Drs Gugenheim et Esna
Rambouillet, 78120
Cabinet Du Dr Christophe Robin
Roanne, 42300
Hopital Victor Provo
Roubaix, 59100
CH de Soissons
Soissons, 02200
Cabinet du Dr Annick Gayou-Joyeux
Talence, 33400
HIA Sainte Anne
Toulon, 83000
Hopital Pierre-Paul Riquet
Toulouse, 31059
CHU Bretonneau
Tours, 37000
CH de Troyes
Troyes, 10000
CH de Valence
Valence, 26000
About this study
Official title: Study on the Dimethyl Fumarate (DMF, Tecfidera®) Persistence of Remitting-relapsing Multiple Sclerosis (RR-MS) Patients Included in the French Patient Support Program (PSP) OroSEP
The primary objective is to compare oral dimethyl fumarate (DMF) persistence at six months in relapsing-remitting multiple sclerosis (RR-MS) participants initiating DMF with and without OroSEP patient support program (PSP), respectively.
The secondary objectives are: to compare oral DMF persistence at one month and three months in RR-MS participants initiating DMF with and without OroSEP PSP, respectively; To compare oral DMF adherence at six months in RR-MS participants initiating DMF with and without OroSEP PSP; To compare at three months and six months the reason of oral DMF discontinuation, in the two groups; To describe the percentage of participants with treatment-related adverse events globally and by class of adverse events, in the two groups of participants; To assess the evolution of participants' anxiety globally and to compare it at inclusion and at six months in participants with and without OroSEP PSP, respectively; To describe participants' satisfaction regarding oral DMF initiation and follow-up globally at six months and to compare it in patients with and without OroSEP PSP, respectively;
For OroSEP PSP group: To assess participants' satisfaction regarding their participation in OroSEP PSP at six months; To assess neurologists' satisfaction regarding their participation in OroSEP PSP, after the last participant last visit of center.
- Conditions
- Multiple Sclerosis, Relapsing-Remitting
- Being tested
- Dimethyl Fumarate, PSP
- Medical subject headings
- Multiple Sclerosis, Relapsing-Remitting
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Dimethyl FumarateDrug
Also called Tecfidera®
DMF as prescribed as standard of care.
PSPOther
PSPs is to support patient care.
| Study group | Role | What they receive |
|---|---|---|
| Standard of Care (SoC) Group | SoC neurologists will include and follow-up all study participants who receive DMF according to their standard of care practice (non-coached participants). Receives: Drug: Dimethyl Fumarate | |
| OroSEP PSP (OPSP) Group | OPSP neurologists will include and follow-up all study participants who receive DMF according to their standard of care practice and the OroSEP PSP (coached participants). Receives: Drug: Dimethyl Fumarate; Other: PSP |
What is being measured
The primary outcome is the main question the study is designed to answer.
Percentage of Participants with Oral Dimethyl Fumarate (DMF) Persistence at 6 Months
Persistence is defined as the percentage of participant still being treated by oral DMF at 6 months, according to routine visit.
Measured: 6 months
Secondary outcomes (11)
Percentage of Participants with Oral Dimethyl Fumarate (DMF) Persistence at Both 1 Month and 3 Months
Persistence is defined as the percentage of participants still being treated by oral DMF at both 1 month and 3 months, according to routine practice.
Measured: 1 month and 3 months
Percentage of Participant's with Adherence at 6 Months
Participant's adherence is assessed through the validated Girerd questionnaire. This is a 6-item self-questionnaire completed by participants with a scale of 0 for "Yes" and 1 for "No" for each question. Points for each question are summed up to obtain a global score between 0 if all the questions are ticked with "Yes" (reflecting a bad adherence), and 6 if all questions are ticked "No" (reflecting a good adherence).
Measured: 6 months
Percentage of Participants by Reason of Oral Dimethyl Fumarate (DMF) Discontinuation at 3 Months and 6 Months
Discontinuation of DMF therapy is defined by the presence of any of the following criteria: definitive discontinuation declared by the physician during routine follow-up visit through electronic case report form (eCRF); a temporary stop declared by the physician during routine visit at 3 months, without DMF resumption declared at 6 months by the physician; a switch to another DMT declared by the physician during routine follow-up visit through eCRF.
Measured: 3 month and 6 months
Percentage of Participants with Adverse Events (AEs)
An AE is any untoward medical occurrence in a patient or clinical investigation participant administered a pharmaceutical product and that does not necessarily have a causal relationship with this treatment. An AE can therefore be any unfavorable and unintended sign (including an abnormal laboratory finding), symptom, or disease temporally associated with the use of a medicinal (investigational) product, whether or not related to the medicinal (investigational) product.
Measured: up to 6 months
Percentage of Participants with Adverse Events (AEs) Related to Treatment
Measured: up to 6 months
Percentage of Participants with Adverse Events (AEs) Leading to Treatment Discontinuation
Measured: up to 6 months
Percentage of Participants with Adverse Events (AEs) of Interest
AEs of interest includes gastrointestinal disorders, flush, lymphopenia.
Measured: up to 6 months
Participant's Anxiety at Inclusion and at 6 Months
Participant's anxiety is assessed through the Generalized Anxiety Disorder - 7 (GAD-7) self-questionnaire. The GAD-7 is a questionnaire that is used primarily to detect possible generalized anxiety disorders, disorders of panic, social anxiety and post-traumatic stress disorder. It is more specifically a self-questionnaire (completed by the participant) consisting of 7 items rated from 0 to 3. The total score is obtained by adding the score obtained to each item (score ranging from 0 to 21). A total score greater than 7 is suggestive of a generalized anxiety disorder.
Measured: 0 months and 6 months
Participant's Satisfaction Regarding Dimethyl Fumarate (DMF) Treatment at 6 Months
Participant's satisfaction regarding DMF treatment is assessed through the validated Treatment Satisfaction Questionnaire for Medication (TSQM-9) score completed by the participant. The TSQM-9, a 9-items questionnaire, designed as a general measure of treatment satisfaction with medication. TSQM items are answered on 5- or 7-point Likert type scale and cover three domains, corresponding to distinct aspects related to the satisfaction of participants with their treatment (effectiveness, convenience and global satisfaction). A score can be obtained for each domain by summing the corresponding items transformed on a 0-100 scale. Higher value indicates more satisfaction, better perceived effectiveness, lower burden associated with better convenience.
Measured: 6 months
Participant's Satisfaction Regarding their Participation in OroSEP Patient Support Program (PSP)
Participant's satisfaction is assessed at Month 6 using a questionnaire completed by the participant consisting of 3 questions. Questions 1 and 2 are assessed using a Likert scale (1-5) with scale range 1= Strongly disagree to 5= Strongly agree. Question 3 is assessed using the net promoter scale (1-7), where 1 indicates "not at all likely" and 7 indicates "extremely likely". Higher values indicate higher satisfaction.
Measured: 6 month
Neurologists' Satisfaction Regarding their Participation in OroSEP Patient Support Program (PSP)
Neurologist's satisfaction is assessed after the last participant last visit of the site center using a 10-item questionnaire, completed by the physician. Question (Q) 1, Q3, Q4, Q6, Q7, Q8= is answered "Yes/No"; Q2= Lack of time, Lack of interest, Patient refused, Forget, No registration form available, Registration process too complicated / Other: specify; Q5= The availability of the call center, The monitoring of patient compliance, The coordination of biological assessments, Other: specify; Q9: 1 bad satisfaction, 10 good satisfaction and Q10 was an open answer.
Measured: up to 6 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted9 Jan 2020
- Study start19 Aug 2019
- Primary completion14 Sep 2022
- Study completion14 Sep 2022
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Multiple Sclerosis, Relapsing-RemittingStudies of the same condition, open and under way.
- More trials run by BiogenThe 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
- 353 participants (actual)
Sponsor and investigators
- Lead sponsor
- Biogen
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- Medical Director, Study director, Biogen
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04221191
- Sponsor's protocol ID
- FRA-BGT-18-11469
- Acronym
- TEC-ADHERE
- Status last verified
- Jul 2023
- First submitted
- 6 Jan 2020
- Last updated
- 1 Aug 2023
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: In accordance with Biogen's Clinical Trial Transparency and Data Sharing Policy on http://clinicalresearch.biogen.com/
Publications
Labauge P, Creange A, Moreau T, Nouvet-Gire J, Pedespan B, Heinzlef O, Texier N, Gros M, Marti C, Ruiz M, Martinez M, Castelnovo G. TEC-ADHERE: Real-World Persistence and Adherence on Dimethyl Fumarate in Patients with Relapsing-Remitting Multiple Sclerosis in the French OroSEP Patient-Support Program. Neurol Ther. 2025 Feb;14(1):177-192. doi: 10.1007/s40120-024-00674-x. Epub 2024 Nov 11.
PubMed 39527163
Study at a glance
From the registry record, last updated by the sponsor on 1 Aug 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Study on the Dimethyl Fumarate (DMF, Tecfidera®) Persistence of Remitting-relapsing Multiple Sclerosis (RR-MS) Patients Included in the French Patient Support Program (PSP) OroSEP
- ClinicalTrials.gov ID
- NCT04221191
- Acronym / sponsor ID
- TEC-ADHERE / FRA-BGT-18-11469
- Conditions
- Multiple Sclerosis, Relapsing-Remitting
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 353 participants (actual)
- Lead sponsor
- BiogenIndustry (pharma, biotech, devices)
- Study start
- 19 Aug 2019 (actual)
- Primary completion
- 14 Sep 2022 (actual)
- Study completion
- 14 Sep 2022 (actual)
- First posted
- 9 Jan 2020 (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.
The primary objective is to compare oral dimethyl fumarate (DMF) persistence at six months in relapsing-remitting multiple sclerosis (RR-MS) participants initiating DMF with and without OroSEP patient support program (PSP), respectively.
The secondary objectives are: to compare oral DMF persistence at one month and three months in RR-MS participants initiating DMF with and without OroSEP PSP, respectively; To compare oral DMF adherence at six months in RR-MS participants initiating DMF with and without OroSEP PSP; To compare at three months and six months the reason of oral DMF discontinuation, in the two groups; To describe the percentage of participants with treatment-related adverse events globally and by class of adverse events, in the two groups of participants; To assess the evolution of participants' anxiety globally and to compare it at inclusion and at six months in participants with and without OroSEP PSP, respectively; To describe participants' satisfaction regarding oral DMF initiation and follow-up globally at six months and to compare it in patients with and without OroSEP PSP, respectively;
For OroSEP PSP group: To assess participants' satisfaction regarding their participation in OroSEP PSP at six months; To assess neurologists' satisfaction regarding their participation in OroSEP PSP, after the last participant last visit of center.
Study design
- Observational model
- Case-control
- Time perspective
- Prospective
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Standard of Care (SoC) Group | – | Drug: Dimethyl FumarateSoC neurologists will include and follow-up all study participants who receive DMF according to their standard of care practice (non-coached participants). |
| OroSEP PSP (OPSP) Group | – | Drug: Dimethyl Fumarate, Other: PSPOPSP neurologists will include and follow-up all study participants who receive DMF according to their standard of care practice and the OroSEP PSP (coached participants). |
Who may qualify
- Ages
- 18 to 55 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult
- Study population
- Study population included participants with RR-MS treated with DMF in clinical practice.
Key inclusion criteria (4 listed)
- Ability to understand the purpose and risks of the study and giving oral informed consent regarding TEC-ADHERE study and authorization to use protected health information (PHI) in accordance with national and local participant privacy regulations;
- Diagnosis of RR-MS;
- Initiating oral DMF according to Summary of Product Characteristics (SmPC) at the inclusion visit;
- Expanded Disability Status Score (EDSS) under 6.
Key exclusion criteria (3 listed)
- Participants with progressive form of Multiple Sclerosis (MS);
- With memory or psychiatric disorders preventing them to complete questionnaires in the study.
- Note: Other protocol defined Inclusion/Exclusion criteria may apply.
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 |
|---|---|---|
| Dimethyl FumarateAlso: Tecfidera®DMF as prescribed as standard of care. | Drug | OroSEP PSP (OPSP) Group, Standard of Care (SoC) Group |
| PSPPSPs is to support patient care. | Other | OroSEP PSP (OPSP) Group |
Primary outcome
Percentage of Participants with Oral Dimethyl Fumarate (DMF) Persistence at 6 Months
Time frame: 6 months
Persistence is defined as the percentage of participant still being treated by oral DMF at 6 months, according to routine visit.
11 secondary outcomes
Percentage of Participants with Oral Dimethyl Fumarate (DMF) Persistence at Both 1 Month and 3 Months
Time frame: 1 month and 3 months
Percentage of Participant's with Adherence at 6 Months
Time frame: 6 months
Percentage of Participants by Reason of Oral Dimethyl Fumarate (DMF) Discontinuation at 3 Months and 6 Months
Time frame: 3 month and 6 months
Percentage of Participants with Adverse Events (AEs)
Time frame: up to 6 months
Percentage of Participants with Adverse Events (AEs) Related to Treatment
Time frame: up to 6 months
Percentage of Participants with Adverse Events (AEs) Leading to Treatment Discontinuation
Time frame: up to 6 months
Percentage of Participants with Adverse Events (AEs) of Interest
Time frame: up to 6 months
Participant's Anxiety at Inclusion and at 6 Months
Time frame: 0 months and 6 months
Participant's Satisfaction Regarding Dimethyl Fumarate (DMF) Treatment at 6 Months
Time frame: 6 months
Participant's Satisfaction Regarding their Participation in OroSEP Patient Support Program (PSP)
Time frame: 6 month
Neurologists' Satisfaction Regarding their Participation in OroSEP Patient Support Program (PSP)
Time frame: up to 6 months
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 1 Aug 2023.
- Derived from this study: PubMed 39527163Labauge P, Creange A, Moreau T, Nouvet-Gire J, Pedespan B, Heinzlef O, Texier N, Gros M, Marti C, Ruiz M, Martinez M, Castelnovo G. TEC-ADHERE: Real-World Persistence and Adherence on Dimethyl Fumarate in Patients with Relapsing-Remitting Multiple Sclerosis in the French OroSEP Patient-Support Program. Neurol Ther. 2025 Feb;14(1):177-192. doi: 10.1007/s40120-024-00674-x. Epub 2024 Nov 11.
- Individual participant dataSharing planned: Yes. In accordance with Biogen's Clinical Trial Transparency and Data Sharing Policy on http://clinicalresearch.biogen.com/
Related trials for Multiple Sclerosis, Relapsing-Remitting
Active, not recruiting
Myrosinase Bioactivated Gglucoraphanin for the Treatment of Neurodegenerative Diseases (GRA-MYR-ND)
PARKINSON DISEASE (Disorder), Multiple Sclerosis (MS) - Relapsing-remitting
Recruiting
Wearable Focal Vibration Therapy on Upper Extremity Function of People With Multiple Sclerosis: A Pilot Study
Multiple Sclerosis (MS) - Relapsing-remitting, Upper Extremity Dysfunction
Not yet recruiting
Treatment of Memory Retrieval Impairments in MS With HDtDCS to the LIFG in a Placebo Controlled Trial
Multiple Sclerosis, Relapsing-remitting Multiple Sclerosis (RRMS)
Recruiting
Monthly Monitoring of Plasma NfL in Treated Relapsing-remitting Multiple Sclerosis to Detect Persistent Infraclinical Disease Activity
Multiple Sclerosis (MS) - Relapsing-remitting
Active, not recruitingPhase 4
Safety and Efficacy Study of Fingolimod in Taiwanese Adults (≥ 20years) With Relapsing Remitting Multiple Sclerosis
Multiple Sclerosis
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.
Medical Director study director
Biogen
63 sites 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, Relapsing-Remitting, run by Biogen at 63 sites in France.
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 3 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 1 Aug 2023. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 63 sites in France. 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?
Percentage of Participants with Oral Dimethyl Fumarate (DMF) Persistence at 6 Months (time frame: 6 months). 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 NCT04221191, which also lists 1 linked publication.
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 1 Aug 2023.