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O estudo clínico NCT06157086 (SEPROS) para Esclerose Múltipla (EM) está recrutando. Consulte a visualização em cartões do Radar de Estudos Clínicos e as ferramentas de descoberta de IA para ver todos os detalhes. Ou pergunte qualquer coisa aqui.
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Assessment of the Quality of Life of Multiple Sclerosis Patients Treated With Ofatumumab in Real-life in France (SEPROS)

Recrutando
Os detalhes do estudo clínico estão disponíveis principalmente em inglês. No entanto, a IA Trial Radar pode ajudar! Basta clicar em 'Explicar o estudo' para visualizar e discutir as informações do estudo no idioma selecionado.
O estudo clínico NCT06157086 (SEPROS) é um ensaio observacional para Esclerose Múltipla (EM). Seu status atual é: recrutando. O estudo começou em 21 de dezembro de 2023 e pretende incluir 294 participantes. Coordenado por Novartis e deve ser concluído em 31 de julho de 2026. Essas informações foram atualizadas no ClinicalTrials.gov em 14 de janeiro de 2025.
Resumo
SEPROS is a non-interventional study, based on primary data collection of MS adult patients who initiated ofatumumab as per neurologist practice and regardless of the study protocol.
Descrição detalhada
This is a non-interventional, prospective (primary data), multicenter study conducted in metropolitan France. The primary objective of this study is to describe the quality of life of MS patients after initiation of treatment with ofatumumab.

In order to form a representative sample of MS patients taking into account the terms of care in France, free or practicing neurologists in healthcare institutions (public or private) in different regions of France will be selected to participate in this study.

The study will enroll adult patients with MS who initiated ofatumumab according to the physician's advice and independently of the study. Patients will be followed from initiation of ofatumumab either until (i) 12 months (± 1month) after initiation of ofatumumab (End of Study), or until (ii) discontinuation of treatment with ofatumumab prior to the completion of the 12-month follow-up (early termination); whichever occurs first (end of study or early termination).

Título oficial

This is a Non-interventional, Prospective, Multicenter Study Conducted in France. The Primary Objective of This Study is to Describe the Quality of Life of MS Patients After Initiation of Treatment With Ofatumumab.

Condições
Esclerose Múltipla (EM)
Outros IDs do estudo
  • SEPROS
  • COMB157GFR06
Número NCT
Data de início (real)
2023-12-21
Última atualização postada
2025-01-14
Data de conclusão (estimada)
2026-07-31
Inscrição (estimada)
294
Tipo de estudo
Observacional
Status
Recrutando
Palavras-chave
MS
Multiple sclerosis
NIS
ofatumumab
Kesimpta
QoL
PRO
Braços / Intervenções
Grupo de participantes/BraçoIntervenção/Tratamento
ofatumumab
MS adult patients who initiated ofatumumab as per neurologist practice and regardless of the study protocol
Ofatumumabe
There is no treatment allocation. Participants with MS that initiated treatment with ofatumumabas per neurologist practice and regardless of the study protocol
Desfecho primário
Medida de desfechoDescrição da medidaPrazo
Quality of life - MUSIQoL questionnaire
The primary objective of this non-interventional study is to describe the quality of life of adult patients with MS treated with ofatumumab in real life, in France, after 12 months of treatment with ofatumumab using the MUSIQoL Quality of Life Questionnaire. The MuSiQoL measures MS-specific quality of life. It comprises 31 items covering 9 domains (activities of daily living, psychological well-being, symptoms, relationships with friends, relationships with family, relationships with the healthcare system, sentimental and sexual life, coping, and rejection). Each item is scored on a 6-point Likert scale. The score on each dimension is obtained by computing the mean of the item scores for that dimension. All dimension scores are linearly transformed to a 0-100 scale. The global index score is computed as the mean of the dimension scores. Higher scores represent higher quality of life.
12 months
Desfecho secundário
Medida de desfechoDescrição da medidaPrazo
Treatment satisfaction of patients treated with ofatumumab using TSQM 9 questionnaire
TSQM -9 is a self-questionnaire used to assess patient satisfaction with their treatment. It is a validated questionnaire and a good predictor of compliance. It explores 4 dimensions of satisfaction (efficacy, side effects, simplicity and overall satisfaction), through 9 questions. Responses are expressed on a 7-point Likert scale to precisely capture the patient's point of view. The responses to the items are aggregated; thus, each dimension is noted between 0 (extremely dissatisfied) and 100 (extremely satisfied).
12 months
Impact of MS on professional activity using the 6-item WPAI questionnaire
The WPAI measures absence, presence, decreased work productivity, and reduction in normal daily activities over the past 7 days. This self-questionnaire is non-specific for a disease and is developed in 6 questions. It works to calculate a health-related deterioration score, which combines the absence score and presence score. This deterioration score is rated between 0 and 1 where 1 corresponds to the maximum score, i.e. stopping work
12 months
Neurologist's decision criteria for initiating ofatumumab and patient involvement in the treatment choice
For each patient included in the study, neurologist's decision criteria for ofatumumab initiation will be collected (i.e., patient characteristics and poor prognosis factors or reasons for treatment switch if applicable) as well as the involvement of the patient in the choice of treatment (yes or no)
Baseline
Clinical evolution of Multiple sclerosis - EDSS score
The Expanded Disability Status Scale (EDSS) is a method of quantifying disability in multiple sclerosis and monitoring changes in the level of disability over time. The EDSS scale ranges from 0 to 10 in 0.5 unit increments that represent higher levels of disability. Scoring is based on an examination by a neurologist.
12 months
Clinical evolution of Multiple sclerosis - Number of patients with relapses
Number of patients with relapses and number of patients with hospitalizations related to the relapse
Up to 12 months
Number of patient adherent to ofatumumab from patient and practitioner perspectives
Number of patient adherent to ofatumumab from patient and practitioner perspectives to be collected
12 months
Ofatumumab discontinuation
Ofatumumab discontinuation by reason to be collected
12 months
Persistence on ofatumumab
Patients still treated with ofatumumab at 6 and 12 months
Month 6, Month 12
Critérios de elegibilidade

Idades elegíveis
Adulto, Adulto mais velho
Idade mínima
18 Years
Sexos elegíveis
Todos
  1. Male or female, 18 years of age or older
  2. Patient with confirmed MS diagnosis
  3. Patient initiating treatment with ofatumumab for the first time
  4. Patient for which the decision to initiate treatment with ofatumumab was made by the doctor (investigator) in accordance with his/her usual practices independently of the study
  5. Patient not opposed to participation in this study
  6. Patient willing and able to complete patient questionnaires

1. Patient treated with ofatumumab in the context of a clinical trial
Contato central do estudo
Contato: Novartis Pharmaceuticals, +41613241111, [email protected]
Contato: Novartis Pharmaceuticals
43 Locais do estudo em 1 países
Novartis Investigative Site, Agen, 47923, France
Recrutando
Novartis Investigative Site, Altkirch, 68130, France
Recrutando
Novartis Investigative Site, Amiens, 80054, France
Recrutando
Novartis Investigative Site, Angers, 49933, France
Recrutando
Novartis Investigative Site, Béthune, 62400, France
Recrutando
Novartis Investigative Site, Bordeaux, 33076, France
Recrutando
Novartis Investigative Site, Brest, 29200, France
Recrutando
Novartis Investigative Site, Cahors, 46000, France
Recrutando
Novartis Investigative Site, Chambéry, 73011, France
Recrutando
Novartis Investigative Site, Compiègne, 60200, France
Recrutando
Novartis Investigative Site, Contamine-sur-Arve, 74130, France
Recrutando
Novartis Investigative Site, Dax, 40107, France
Recrutando
Novartis Investigative Site, La Rochelle, 17019, France
Recrutando
Novartis Investigative Site, La Seyne-sur-Mer, 83500, France
Recrutando
Novartis Investigative Site, Le Bouscat, 33110, France
Recrutando
Novartis Investigative Site, Le Coudray, 28630, France
Recrutando
Novartis Investigative Site, Lens, 62307, France
Recrutando
Novartis Investigative Site, Libourne, 33505, France
Recrutando
Novartis Investigative Site, Lille, 59000, France
Recrutando
Novartis Investigative Site, Lyon, 69275, France
Recrutando
Novartis Investigative Site, Mantes-la-Jolie, 78200, France
Recrutando
Novartis Investigative Site, Marseille 01, 13001, France
Recrutando
Novartis Investigative Site, Mont-de-Marsan, 40024, France
Recrutando
Novartis Investigative Site, Montluçon, 03100, France
Recrutando
Novartis Investigative Site, Montpellier, 34295, France
Recrutando
Novartis Investigative Site, Mulhouse, 68100, France
Recrutando
Novartis Investigative Site, Nîmes, 30029, France
Recrutando
Novartis Investigative Site, Orsay, 91400, France
Recrutando
Novartis Investigative Site, Paris, 75017, France
Recrutando
Novartis Investigative Site, Paris, F-75571, France
Recrutando
Novartis Investigative Site, Pointe à Pitre, 97159, France
Recrutando
Novartis Investigative Site, Poissy, 78303, France
Recrutando
Novartis Investigative Site, Pringy, 74374, France
Recrutando
Novartis Investigative Site, Reims, 51092, France
Recrutando
Novartis Investigative Site, Rennes, 35043, France
Recrutando
Novartis Investigative Site, Saint-Maur-des-Fossés, 94100, France
Recrutando
Novartis Investigative Site, Saverne, 67700, France
Recrutando
Novartis Investigative Site, Sélestat, 67600, France
Recrutando
Novartis Investigative Site, Strasbourg, 67000, France
Recrutando
Novartis Investigative Site, Toulouse, 31059, France
Recrutando
Novartis Investigative Site, Tours, 37044, France
Recrutando
Novartis Investigative Site, Valence, 26953, France
Recrutando
Novartis Investigative Site, Villeurbanne, 69100, France
Recrutando