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Rituximab vs Placebo for Maintenance in Systemic Sclerosis - Interstitial Lung Disease (MAINRITSyS)

14 settembre 2026 aggiornato da: Assistance Publique - Hôpitaux de Paris
The purpose of this study is to determine whether Rituximab is safe and effective as a maintenance strategy in individuals with stabilized systemic sclerosis in adults.

Panoramica dello studio

Stato

Non ancora reclutamento

Intervento / Trattamento

Descrizione dettagliata

Systemic sclerosis (SSc) is a rare autoimmune connective tissue-disease. Interstitial lung disease (ILD) is a common manifestation and a leading cause of death in SSc.

Rituximab (RTX) is commonly used in SSc-ILD induction treatment and recent trials have now fully demonstrated its safety and efficacy as an induction treatment. The DESIRES trial reported that RTX-induction was associated with a 24-week stabilization of FVC. As evaluated by the FVC at 24 weeks from baseline, 25 patients with SSc-ILD treated with RTX were significantly improved compared with 23 patients treated with placebo (0.09% vs -2.87%; [95%CI 0.08-5.84]; p < 0.05). Recently, the RECITAL trial showed the absence of difference between induction treatment with cyclophosphamide (CYC) and RTX in ILD including SSc-ILD. Indeed, both RTX and CYC resulted in an improvement in FVC (97 ± 234mL and 99 ± 329mL respectively) at 24 weeks, without significant statistical difference in 101 subjects. Furthermore, the EVER-ILD study, also very recently presented, reported a beneficial of RTX in addition to mycophenolate mofetil (MMF) over RTX in CTD-ILD. Altogether with previous European database studies which analyzed the very common usage of RTX as induction therapy in SSc, these studies have confirmed its efficient and safe role as an induction treatment in SSc-ILD.

Still, the impact of re-treatment with RTX in maintaining ILD-stabilization has never been studied and deserve to be studied.

The hypothesis that drives the MAINRITSyS is that RTX maintains ILD stabilization in SSc-ILD.

Tipo di studio

Interventistico

Iscrizione (Stimato)

120

Fase

  • Fase 2

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Backup dei contatti dello studio

Luoghi di studio

    • Île-de-France Region
      • Paris, Île-de-France Region, Francia, 75014

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto
  • Adulto più anziano

Accetta volontari sani

No

Descrizione

Inclusion Criteria:

  • Adult patient (≥ 18 years old),
  • Patient with a diagnosis of SSc, as defined by the ACR/EULAR 2013 criteria (cf. Table 2) (6)
  • Patient with ILD identified on the basis of a HRCT, obtained within 12 months before screening, that showed fibrosis affecting at least 10% of the lungs,
  • SSc-ILD induction with RTX, either twice 1000 mg two weeks apart, or 375 mg/m2 four times 4 weeks apart.

The interval between the last induction dose and the first maintenance dose should be 6 months +/- 15 days.

  • Patient with stabilized SSc-ILD following RTX induction treatment as defined by the absence of worsening respiratory symptoms, an absolute decline of FVC of < 5% of the predicted value, an absence of absolute decline of DLCO (corrected for hemoglobin) of < 10% related to SSc-ILD, and absence of radiological evidence of disease progression on HRCT(97)
  • All required vaccinations must have been carried out at least 4 weeks before D0. According to recommendations, prophylaxis against pneumocystis is recommended for scleroderma, but not mandatory.
  • Woman of childbearing potential should have reliable contraception* for the 12 months' duration of the study's treatment and 12 months after last administration,
  • Patient able to give written informed consent prior to participation in the study,
  • Affiliation to a social security scheme (profit or being entitled). AME is not accepted.

Exclusion Criteria

  • Forced vital capacity < 40% of the predicted value
  • Diffusion capacity of the lung for carbon monoxide (DLCO) (corrected for hemoglobin) < 30% of the predicted value.
  • Contra-indication or anaphylaxis toward RTX
  • Contra-indication to auxiliary medicinal products
  • Cyclophosphamide, tacrolimus, ciclosporin, or voclosporin during the 2 months prior to screening or during screening
  • Any biologic therapy (including other anti-CD20, anti-CD19, or anti-plasma cell) such as, but not limited to, belimumab, ustekinumab, anifrolumab, secukinumab, or atacicept during the 2 months prior to screening or during screening
  • Inhibitors of Janus-associated kinase (JAK), Bruton's tyrosine kinase (BTK), or tyrosine kinase 2 (TYK2), including baricitinib, tofacitinib, upadacitinib, filgotinib, ibrutinib, or fenebrutinib or any investigational agent during the 2 months prior to screening or during screening
  • Any live vaccine during the 28 days prior to screening or during screening
  • High risk for clinically significant bleeding or any condition requiring plasmapheresis, IV immunoglobulin, or acute blood product transfusions during the 28 days prior the screening
  • Active infection with SARS-CoV-2 or absence of COVID-19 vaccination within the last six months (this criteria will be updated at the time of submission to European Agency to be in adequation with national recommendation at the time of submission).
  • Significant or uncontrolled medical disease which, in the investigator's opinion, would preclude patient participation
  • HIV infection : for participants with unknown HIV status (if the previous tests date more than 3 months), HIV testing will be performed locally at screening.
  • Tuberculosis (TB) infection: Testing for latent TB will be performed locally at screening if required by local regulations or in accordance with local clinical practice. Latent TB after completion of appropriate treatment is not exclusionary
  • Active infection of any kind, excluding fungal infection of the nail beds.
  • History of serious recurrent or chronic infection
  • History of progressive multifocal leukoencephalopathy (PML)
  • History of cancer, including solid tumors, hematological malignancies, and carcinoma in situ, within the past 5 years. Participants with non-melanomatous carcinomas of the skin that have been treated or excised and have resolved are eligible.
  • Major surgery requiring hospitalization during the 4 weeks prior to screening or during screening
  • Current alcohol or drug abuse or history of alcohol or drug abuse within 12 months prior to screening or during screening
  • History of severe allergic or anaphylactic reactions to monoclonal antibodies or known hypersensitivity to any component of the RTX infusion
  • Any of the following laboratory parameters:

    • AST or ALT above 2.5 upper limit normal range
    • Neutrophils <1.5x103/mL
    • Positive hepatitis B surface antigen (HBsAg)
    • Positive hepatitis C serology Participants with positive hepatitis C antibody test result with no detectable hepatitis C virus (HCV) RNA for at least 6 months after completion of antiviral therapy are eligible but will require monthly HCV RNA monitoring until 12 months after the last dose of RTX or placebo.
  • Pregnancy or breastfeeding
  • Participation in another interventional study or being in the exclusion period at the end of a previous study.
  • Participants under court supervision, guardianship, or conservatorship.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Triplicare

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Rituximab
500mg of i.v rituximab at M0, M6 and M12
500mg i.v at M0, M6 and M12
Comparatore placebo: Placebo
500mg of i.v placebo at M0, M6 and M12
500mg i.v at M0, M6 and M12

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
changes in forced vital capacity (FVC) from baseline to Month 18 of randomisation.
Lasso di tempo: 18 months
PFTs: changes in forced vital capacity (FVC)
18 months

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Mortality up to 18 months
Lasso di tempo: 18 months
18 months
Occurrence of Adverse Events
Lasso di tempo: At 6, 12 and 18 months
Occurrence of adverse events, overall and occurring at time of perfusion (day 0, and 6, 12 and 18 months)
At 6, 12 and 18 months
Occurrence of Adverse Events
Lasso di tempo: At 6, 12 and 18 months
The number of adverse events, expressed according to the Common Terminology Criteria for Adverse Events (CTCAE): CTCAE toxicity grading system per patient-year at month 6, 12, and 18, for the following adverse events combined: death (all causes), grade 2 or higher leukopenia or thrombocytopenia, grade 3 or higher infections, hospitalization resulting either from the disease or from a complication due to the study treatment.
At 6, 12 and 18 months
Occurrence of AE of specific interest previously mentioned at 6, 12 and 18 months
Lasso di tempo: At 6, 12 and 18 months
At 6, 12 and 18 months
Change in gammaglobulin, lymphocytes and CD19 levels at 6, 12 and 18 months
Lasso di tempo: At 6, 12 and 18 months
At 6, 12 and 18 months
Change from baseline in DLCO over 6, 12, and 18 months
Lasso di tempo: At 6, 12 and 18 months
At 6, 12 and 18 months
Change from baseline in TLC over 6, 12, and 18 months
Lasso di tempo: At 6, 12 and 18 months
At 6, 12 and 18 months
Further analyses on TLC
Lasso di tempo: At 6, 12 and 18 months
Absolute categorical change of % TLC at 6, 12 and 18 months (decrease by >5%, increase by >5% and change within <5%) Absolute categorical change of % TLC at 6, 12 and 18 months (decrease by >10%, increase by >10% and change within <10%)
At 6, 12 and 18 months
Change from in 6-min walk test distance over 6, 12 and 18 months
Lasso di tempo: At 6, 12 and 18 months
At 6, 12 and 18 months
Further analyses on FVC
Lasso di tempo: At 6, 12 and 18 months
  • Absolute categorical change of % FVC at 6, 12 and 18 months (decrease by >5%, increase by >5% and change within <5%)
  • Absolute categorical change of % FVC at 6, 12 and 18 months (decrease by >10%, increase by >10% and change within <10%)
At 6, 12 and 18 months
Progression-free survival (composite endpoint of mortality, transplant, treatment failure or decline in FVC >10% compared to baseline) over 6, 12 and 18 months
Lasso di tempo: At 6, 12 and 18 months
At 6, 12 and 18 months
Treatment failure (as determined by need for transplant or rescue therapy) at 6, 12 and 18 months
Lasso di tempo: At 6, 12 and 18 months
At 6, 12 and 18 months
INBUILD progression (as determined by the INBUILD criteria for ILD progression(73)) at 6, 12 and 18 months
Lasso di tempo: At 6, 12 and 18 months
At 6, 12 and 18 months
Change from baseline in capillary oxygen saturation (SpO2) at 6, 12 and 18 months
Lasso di tempo: At 6, 12 and 18 months
At 6, 12 and 18 months
Changes from baseline to 18 months in HRCT of chest images
Lasso di tempo: At 18 months
At 18 months
Proportions of patients who achieved 20%, 30%, 40%, 50% ,60%, 70%, 80%, 90% and 100% response criteria according to revised CRISS at 6, 12 and 18 months
Lasso di tempo: At 6, 12 and 18 months
At 6, 12 and 18 months
Changes in physicians visual analogue scales over 18 months.
Lasso di tempo: at 0, 6, 12, 18 months
These scales range from 0 (minimum) to ten (maximum) points and will be performed at day 0, at 6, 12, and 18 months. Higher score mean worse outcome
at 0, 6, 12, 18 months
Changes in patients' visual analogue scales over 18 months.
Lasso di tempo: At 0, 6, 12, and 18 months
These scales range from 0 (minimum) to ten (maximum) points and will be performed at day 0, at 6, 12, and 18 months. Higher score mean better outcome
At 0, 6, 12, and 18 months
Changes in mRSS at 6, 12, and 18 months
Lasso di tempo: At 6, 12 and 18 months
Higher score mean worse outcome.
At 6, 12 and 18 months
Proportion of patients who improved mRSS at 6, 12 and 18 months after randomisation.
Lasso di tempo: At 6, 12 and 18 months
At 6, 12 and 18 months
Proportion of patients with an active disease according to the European scleroderma trials and research group (EUSTAR) SSc activity index at 6, 12 and 18 months after randomisation
Lasso di tempo: At 6, 12 and 18 months
At 6, 12 and 18 months
Saint Georges Respiratory Hospital Questionnaire at day 0, and at 6, 12, and 18 months after randomisation.
Lasso di tempo: At 0, 6, 12 and 18 months
These questionnaires are self-administered questionnaires assessing the perception of lung disease by the patients. These scales range from 0 (minimum) to one hundred (maximum) points. Higher score mean worse outcome
At 0, 6, 12 and 18 months
King Brief's Interstitial Lung Disease questionnaire at day 0, and at 6, 12, and 18 months after randomisation.
Lasso di tempo: at 0, 6, 12, and 18 months
These questionnaires are self-administered questionnaires assessing the perception of lung disease by the patients. These scales range from 0 (minimum) to 100 (maximum) points. Higher score mean better outcome
at 0, 6, 12, and 18 months
Short Form-36 (SF-36) health questionnaire
Lasso di tempo: At 0, 6, 12 and 18 months
SF36 : 0 à 100 - These scales range from 0 (minimum) to 100 (maximum) points. Higher score mean better outcome - to assess Quality of life
At 0, 6, 12 and 18 months
EuroQol-5 Domain (EQ5D5L) health questionnaire
Lasso di tempo: At 0, 6, 12 and 18 months
EQ5D5L : The EQ-5D-5L instrument comprises five dimensions: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression. Each dimension is rated on a five-point scale, from 1 (no problems) to 5 (extreme problems), with higher scores reflecting worse health status. To assess quality of life.
At 0, 6, 12 and 18 months
Scleroderma skin patients reported outcome (SSPRO) at day 0, and at 6, 12 and 18 months after randomisation.
Lasso di tempo: At 0, 6, 12 and 18 months
At 0, 6, 12 and 18 months
HAQ-DI and SHAQ scales at day 0, and at 6, 12 and 18 months after randomisation. These scales range from 0 (minimum) to 3 (maximum) points. Higher score mean worse outcome
Lasso di tempo: At 0, 6, 12 and 18 months
At 0, 6, 12 and 18 months
Total corticosteroid requirement at 6, 12 and 18 months
Lasso di tempo: At 6, 12 and 18 months
At 6, 12 and 18 months
Levels of prespecified biomarkers (KL-6, SP-D, MUC1, SFTPD, CCL18 and CXCL4) at months 6, 12 and 18 months.
Lasso di tempo: At 6, 12 and 18 months
At 6, 12 and 18 months
Presence of anti-RTX-antibody at months 6, 12 and 18.
Lasso di tempo: At 6, 12 and 18 months
At 6, 12 and 18 months
Dosage of plasma and serum residual concentration of RTX at months 6, 12 and 18
Lasso di tempo: At 6, 12 and 18 months
At 6, 12 and 18 months
Hospitalisation for respiratory cause over the duration of the trial
Lasso di tempo: At 18 months
At 18 months
Time to first hospitalisation for respiratory cause
Lasso di tempo: At 18 months
At 18 months
Time to death
Lasso di tempo: At 18 months
At 18 months
Time to first acute ILD exacerbation
Lasso di tempo: At 18 months
At 18 months

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Investigatori

  • Cattedra di studio: Luc MOUTHON, MD, PhD, AP-HP - Hôpital Cochin 27 Rue du Faubourg Saint Jacques 75014 France

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

1 ottobre 2026

Completamento primario (Stimato)

1 maggio 2030

Completamento dello studio (Stimato)

1 marzo 2031

Date di iscrizione allo studio

Primo inviato

9 luglio 2026

Primo inviato che soddisfa i criteri di controllo qualità

14 settembre 2026

Primo Inserito (Effettivo)

18 settembre 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

18 settembre 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

14 settembre 2026

Ultimo verificato

1 settembre 2026

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • APHP240909
  • 2025 (Sovvenzione/contratto NIH degli Stati Uniti: Faculty of Social Sciences Scientific Grant at the University of Gdańsk)
  • 2025-521331-36-00 (Ctis)

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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