Phase
Condition
N/ATreatment
Immediate Azathioprine (1st attack)
Standard of care
Immediate Rituximab (1st attack)
Clinical Study ID
Ages 6-17 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Children < 18 years old and ≥ 6 years old at baseline
Children weight ≥ 20 kg
All ADS with confirmed anti-MOG-Abs at onset including any acute neurologic symptomwith a duration of more than 24H of inflammatory causes (including optic neuritis,transverse myelitis, rhombencephalitis, ADEM, NMOSD) Without any previous treatmentother than steroids
Informed consent signed by both parents and the child
Expanded Disability Status Scale (EDSS) < 5.5
Affiliated to French social security regime
Exclusion
Exclusion Criteria:
Current infection with SARS-COV2 (positive PCR)
Any prior allergy to azathioprine or rituximab with hypersensitivity to activesubstances, murine proteins or to any of the excipients.
Any prior history of uncontrolled cancer during the last 2 years
Uncontrolled infections (Hepatitis B, C and HIV)
Any prior history of cardiac dysfunction and/or hypertension
Any progressive or non-relapsing form demyelinating diseases
Any previous treatment with natalizumab, daclizumab, fingolimod, methotrexate,cyclosporine, mycophenolate mofetil, rituximab in the last 6 months, or determinedby the treating physician to have residual immune suppression from these or otherimmunosuppressive treatments
CD4+, CD8+, or CD19+ absolute cell count, wbc, neutrophiles in blood at screeningbelow lower limits of normal (LLN)
Creatinine>30µmol/L
Platelets <70 000mm3
Haemoglobin < 8g/dL
Acute renal insufficiency (clearance < 30 ml/min)
Prior documented history of hemostase perturbation (TP and/or TCA more than twice ofthe witnesse's TP and/or TCA)
Prior documented history of increased liver enzyme level (ASAT and/or ALAT) > 2N.
TP <70%
Total bilirubin > 2N
Any patient with allopurinol treatment and immunosupressive treatment withconcomitant use of xanthine oxidase inhibitors (e.g. allopurinol,oxipurinol/thiopurinol, febuxostat)
Patients with two inactive TPMT or NUDT15 alleles (homozygous deficient or doubleheterozygote)
Pregnancy or lactating woman or wish for future pregnancy
Refusal to have a highly effective contraception during traitment and for one year (12 months) after the end of the experimental treatment
participation to another interventional study within 5 half-lives prior to baseline.
Active, severe infections (including tuberculosis, HBV and HCV, HIV, herpes, VZV,EBV and CMV)
Psychosis not controlled by treatment
Patients with Lesch Nyhan syndrome
Pheochromocytoma
Scleroderma
Untreated peptic ulcer
Myasthenia gravis
Any other medical illness or disability that, in the opinion of the investigator,would compromise effective trial participation
Study Design
Study Description
Connect with a study center
CHU Besançon
Besançon,
FranceSite Not Available
CHU Bordeaux
Bordeaux,
FranceSite Not Available
CHU Brest
Brest,
FranceSite Not Available
HCL de Bron
Bron,
FranceSite Not Available
Hôpital Bicêtre
Le Kremlin Bicetre, 94270
FranceActive - Recruiting
CHRU Lille
Lille,
FranceSite Not Available
CHU Monptellier
Montpellier,
FranceSite Not Available
CHU Strasbourg
Strasbourg,
FranceSite Not Available
CHU Toulouse Purpan
Toulouse,
FranceSite Not Available
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