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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.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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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

Other trials in France

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.

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 groups in NCT04221191
Study groupRoleWhat they receive
Standard of Care (SoC) GroupSoC 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) GroupOPSP 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.

  1. 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)
  1. 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

  2. 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

  3. 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

  4. 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

  5. Percentage of Participants with Adverse Events (AEs) Related to Treatment

    Measured: up to 6 months

  6. Percentage of Participants with Adverse Events (AEs) Leading to Treatment Discontinuation

    Measured: up to 6 months

  7. Percentage of Participants with Adverse Events (AEs) of Interest

    AEs of interest includes gastrointestinal disorders, flush, lymphopenia.

    Measured: up to 6 months

  8. 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

  9. 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

  10. 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

  11. 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.

  1. First posted9 Jan 2020
  2. Study start19 Aug 2019
  3. Primary completion14 Sep 2022
  4. Study completion14 Sep 2022

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
Case-control
Time perspective
Prospective
Enrolment
353 participants (actual)
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

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.

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