MedPath

Baricitinib in the Treatment of New-onset Juvenile Dermatomyositis (MYOCIT)

Phase 2
Recruiting
Conditions
Juvenile Dermatomyositis
Interventions
Biological: pharmacokinetics study
Biological: dosage of cytokines
Biological: transcriptomic analysis
Behavioral: Parent version of the Child Health Questionnaire (CHQ)
Behavioral: Childhood Health Assessment Questionnaire
Biological: Pregnancy test
Registration Number
NCT05524311
Lead Sponsor
Assistance Publique - Hôpitaux de Paris
Brief Summary

The MYOCIT study aims to evaluate the efficacy and safety of baricitinib in association with corticosteroids in new-onset patients with juvenile dermatomyositis (JDM) in a phase II trial with the objective to obtain a better efficacy than the conventional combination methotrexate (MTX) and corticosteroids over the 24 week study period. Thus, the investigators hypothesize that baricitinib could be used as a first line treatment in all forms of DMJ, including the most severe one, with a good safety profile.

Detailed Description

Juvenile dermatomyositis (JDM) is a rare and severe paediatric-onset idiopathic inflammatory myopathy, associated with significant morbidity and mortality. The combination of corticosteroids and methotrexate (MTX) is recommended in new-onset JDM according to one randomized trial. However, in this trial, treatment failures were reported in 13/46 (28%) patients and severe JDM, (cutaneous or gastrointestinal ulceration, interstitial pulmonary disease, cardiomyopathy) were not taken into account. These data emphasize the need for a more efficient first-line treatment. Considering: 1) the strong implication of type IFN-I in the pathophysiology of JDM 2) the report of the efficacy and safety of JAK inhibitors (JAKis) (baricitinb, tofacitinib) in about 50 refractory DM patients, and 9 JDM, a trial which evaluates the efficacy and safety of baricitinib in combination with corticosteroids in new-onset JDM is warranted.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
16
Inclusion Criteria
  • Patient aged 3-18 years with new-onset juvenile dermatomyositis, according to the ENMC 2018 dermatomyositis classification criteria
  • Muscle weakness at MMT and/or CMAS (MMT < 74 and/or CMAS < 45)
  • Seropositivity or vaccination for chickenpox
  • For patients of childbearing age (following menarche) : Negative βHCG and effective method of contraception (sexual abstinence, hormonal contraception, intrauterine device or hormone-releasing system, cap, diaphragm or sponge with spermicide, condom) until the 7 days after administration of the last dose of Baricitinib
  • Informed consent form signed by the patient or child' s parents Patient affiliated to a social security regime

Exclusion Criteria

  • Amyopathic dermatomyositis (without muscle weakness)
  • Inability to be treated by oral way or to take pills
  • Previous treatment with JAK inhibitor
  • Previous treatment of JDM with immunosuppressive drugs or biologics other than corticosteroids. Previous treatment with prednisone was allowed for no more than 1 month.
  • Previous history of cancer
  • Live vaccine within the 4 weeks before starting baricitinib therapy
  • Current, or recent (< 4 weeks prior to baseline) of active infections according to investigator appreciation, but necessarily, including HBV, HCV, HIV, tuberculosis.
  • Positive blood CMV PCR
  • Creatinine clearance < 40 ml/min
  • Lymphocytes < 0,5x109 cell/L and Neutrophils < 1x109 cell/L
  • Hemoglobin < 8 g/dL
  • Symptomatic herpes herpes simplex infection within 12 weeks prior to inclusion
  • History of thrombosis or considered at high risk of venous thrombosis by the investigator
  • Presence of severe JDM-related involvements: cardiovascular (requiring vasopressive drug and/or intensive care unit), respiratory (requiring oxygen and/or intensive care unit), gastrointestinal (requiring abdominal surgery).
  • History of severe non-related JDM involvement: cardiovascular, respiratory, hepatic, gastrointestinal, endocrine, hematological, neurological or neuropsychiatric disorders or any other serious and/or instable illness that, in the opinion of the investigator, could constitute an unacceptable risk, when taking baricitinib.
  • Actual or in project of pregrancy and breast-feeding until the 7 days after administration of the last dose of Baricitinib
  • Patient on AME (state medical aid)
  • Participation in another interventional study involving human participants or being in the exclusion period at the end of a previous study involving human participants
Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Baricitinibpharmacokinetics study-
Baricitinibdosage of cytokines-
Baricitinibtranscriptomic analysis-
BaricitinibParent version of the Child Health Questionnaire (CHQ)-
BaricitinibChildhood Health Assessment Questionnaire-
BaricitinibPregnancy test-
BaricitinibBaricitinib-
Primary Outcome Measures
NameTimeMethod
PRINTO 20 (Paediatric Rheumatology INternational Trials Organisation scale)At week 24

Achievement of the validated juvenile dermatomyositis PRINTO 20 level of improvement. PRINTO 20 level of improvement is defined as a 20% or greater improvement in three or more of the six variables of the juvenile dermatomyositis core set, with one or no variable worsening by more than 30% (muscle strength can not be the variable worsening) :

1. muscle strength, assessed with the Childhood Myositis Assessment Scale (CMAS),

2. physician's global assessment of the patient's disease activity (Physician's VAS)

3. global disease activity assessment through the Disease Activity Score (DAS)

4. functional ability through the Childhood Health Assessment Questionnaire (C-HAQ)

5. parent's global assessment of the child's overall wellbeing (Parent's VAS)

6. health-related quality of life, through the parent version of the Child Health Questionnaire (CHQ-Phs) A higher score is 100% and means a better outcome, a lower score is 0% and means a worse result.

Secondary Outcome Measures
NameTimeMethod
Pharmacokinetics (PK) study with through concentrationAt weeks 4, 8, 12, and 24

Correlation between through concentration Ctrough, in ng/mL (PK parameter of baricitinib) and disease activity 's scores

PRINTO 20 Paediatric Rheumatology INternational Trials Organisation scale - level 20At week 4, 8, 12 and 16

achievement of the validated juvenile dermatomyositis PRINTO 20 level ; reaching a minimum of 20 % a higher score is 100% and mean a better outcome a lower score is 0% and means a worse result

Pharmacokinetics studyAt weeks 4, 8, 12, and 24

Non-compartmental analysis of baricitinib

dosage of cytokinesAt inclusion, weeks 4 and 24

Measurement of serum IFN -, IFN-γ, IL-1β, IL-4, Il-5, IL-6, IL-8, IL-10, IL-12p70, IL-22, TNF α

transcriptomic analysisAt inclusion, weeks 4 and 24

Study of genes expression within 800 genes related to immunity

BiopsyAt inclusion, weeks 4 and 24

Assessment of muscle biopsies according to the internationally validated score system

PRINTO 50 Paediatric Rheumatology INternational Trials Organisation scale - level 50At week 4, 8, 12 and 16

achievement of the validated juvenile dermatomyositis PRINTO 50 level ; reaching a minimum of 50 % a higher score is 100% and mean a better outcome a lower score is 0% and means a worse result

PRINTO 70 Paediatric Rheumatology INternational Trials Organisation scale - level 70At week 4, 8, 12 and 16

achievement of the validated juvenile dermatomyositis PRINTO 70 level ; reaching a minimum of 70 % a higher score is 100% and mean a better outcome a lower score is 0% and means a worse result

PRINTO 90 Paediatric Rheumatology INternational Trials Organisation scale - level 90At week 4, 8, 12 and 16

achievement of the validated juvenile dermatomyositis PRINTO 90 level ; reaching a minimum of 90 % a higher score is 100% and mean a better outcome a lower score is 0% and means a worse result

Total Improvement Score (TIS)At inclusion, weeks 4, 8, 12, 16 and 24

Relative and absolute variations of TIS. The TIS is the sum of the improvement in each of the six core set measures of disease activits The minimum score is 0 (worse) and maximum score is 100 (better) A major response is defined by a score \> 70 A moderate response is defined by a score \> 45 A minimal response is defined by a score \> 30

Clinically inactive diseaseAt weeks 4, 8, 12 and 24

according to the PRINTO criteria

Dose of corticosteroidAt week 24

Dose tapering at 6 months

Cutaneous Dermatomyositis Disease Area and Severity Index (CDSAI)At inclusion, weeks 4, 8, 12, 16 and 24

assess skin activity and damage across multiple body regions in patients with dermatomyositis

Myositis Disease Activity Assessment VAS (MYOACT)At inclusion, weeks 4, 8, 12, 16 and 24

Assess Relative and absolute variations of extramuscular activity

interstitial lung diseaseAt inclusion and at week 24

Assessed by improvement of at least 10% of FCV, PTC, and DLCO and/or improvement of Lung tomodensitomery according to a specific scale

Pharmacokinetics (PK) study with maximal concentrationAt weeks 4, 8, 12, and 24

Correlation between maximal concentration Cmax in ng/mL (PK parameter of baricitinib) and disease activity 's scores

Pharmacokinetics (PK) study with area under the curveAt weeks 4, 8, 12, and 24

Correlation between area under the curve AUC in ng.h/ml (PK parameter of baricitinib) and disease activity 's scores

Trial Locations

Locations (13)

Hôpital Femme Mère Enfant

🇫🇷

Bron, France

Hôpital Pellegrin

🇫🇷

Bordeaux, France

Hôpital Jeanne de Flandre

🇫🇷

Lille, France

Hôpital La Timone

🇫🇷

Marseille, France

Hôpital Brabois

🇫🇷

Nancy, France

Hôpital de Hautepierre

🇫🇷

Strasbourg, France

Hôpital du Kremlin-Bicêtre

🇫🇷

Paris, France

Hôpital Robert Debré

🇫🇷

Paris, France

Hôpital Necker - Enfants malades : service de dermatologie

🇫🇷

Paris, France

Hôpital Trousseau

🇫🇷

Paris, France

Hôpital Purpan

🇫🇷

Toulouse, France

Hôpital Villeneuce

🇫🇷

Montpellier, France

Hopital Necker - Enfants malades : unité d'immuno-hématologie et rhumatologie

🇫🇷

Paris, France

© Copyright 2025. All Rights Reserved by MedPath