Rituximab in Patients With Acute Rheumatic Fever (AGRAF-2)
Rheumatic Heart Disease in Children
About this trial
This is an interventional treatment trial for Rheumatic Heart Disease in Children
Eligibility Criteria
Inclusion Criteria: Children aged between >= 5 and < 17 years old; Diagnosed acute rheumatic fever with at least one progressive rheumatic valvular lesion confirmed through a cardiac echography. Informed consent, signed and dated by both parents or legal guardians of the patient Exclusion Criteria: Simultaneous active infection, such as HIV, hepatitis B, C, tuberculosis, Epstein-Barr virus (EBV), or history of frequent, unusual or serious infections ; Pathologies likely to affect immunity (cancer, multiple sclerosis, diabetes, other auto-immune diseases) Recent history of drug administration that may affect the immune system, for the past 4 weeks (immunosuppressive drugs, corticosteroids, anticancer drugs); Hypersensitivity reaction to rituximab or one of its components. Hypersensitivity to penicillin History of monoclonal antibodies administration Recent vaccination (less than a month) or planned within the 12 months after randomization; History of heart failure Renal failure with a creatinine clearance <45 ml/min/1,73m² Pregnancy (a negative urinary test is necessary for women who had their first menstruations or aged 14 years old and more) Patients diagnosed with Guillain-Barré syndrome Patient with at least one of the following biological features : Hemoglobin < 8,5 g/dL, Platelets < 100 G/L, Neutrophils < 1,5 G/L, Leucocytes < 3 G/L, AST or ALT increased > 2,5 the normal superior limit) Any acute or chronic infection clinically significant which would limitate the patient's capacity to follow up the study protocol, which remains under appreciation of the investigator. Any participation in another clinical trial in the 6 months before the pre-randomization visit
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
Rituximab plus standard of care (RTX)
Standard of care treatment (Control)
Rituximab i.v of two perfusions (375 mg/m²) administered in a 14 day-interval added to a standard of care treatment
Standard of care treatment