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Rituximab in Patients With Acute Rheumatic Fever (AGRAF-2)

Primary Purpose

Rheumatic Heart Disease in Children

Status
Not yet recruiting
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
Rituximab added to standard of care treatment
standard of care treatment
Sponsored by
Paris Cardiovascular Research Center (Inserm U970)
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Rheumatic Heart Disease in Children

Eligibility Criteria

5 Years - 17 Years (Child)All SexesDoes not accept healthy volunteers

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

    Arm Type

    Experimental

    Active Comparator

    Arm Label

    Rituximab plus standard of care (RTX)

    Standard of care treatment (Control)

    Arm Description

    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

    Outcomes

    Primary Outcome Measures

    Rheumatic valvular lesions rate
    Rheumatic valvular lesions rate, measured by echocardiography

    Secondary Outcome Measures

    Incidence of rheumatic valvular lesions
    Rate of rheumatic valvular lesions will be compared between groups
    Serious adverse events rates
    Serious adverse events rate will be compared between groups

    Full Information

    First Posted
    December 15, 2022
    Last Updated
    January 3, 2023
    Sponsor
    Paris Cardiovascular Research Center (Inserm U970)
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05682196
    Brief Title
    Rituximab in Patients With Acute Rheumatic Fever
    Acronym
    AGRAF-2
    Official Title
    Open-label, Randomized Controlled Trial to Assess Efficacy and Safety of Rituximab in Patients With Acute Rheumatic Fever in Africa
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    January 2023
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    February 1, 2023 (Anticipated)
    Primary Completion Date
    September 30, 2024 (Anticipated)
    Study Completion Date
    February 1, 2025 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Paris Cardiovascular Research Center (Inserm U970)

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    Acute Rheumatic Fever is an autoimmune inflammatory post-infectious syndrome, mainly caused by type A streptococcus. It is characterized as an inadequate immune response. It may provoke carditis, combined with articular, skin and neurologic signs. Only carditis, prevalent in 60% of acute rheumatic diseases, may provoke valvular sequels, which define rheumatic cardiopathy. Antibiotherapy based on penicillin is the standard treatment of both acute rheumatic fever and its prevention. Although no anti-inflammatory treatment has proved its efficacy, with or without steroids anti-inflammatory treatments are administered in acute episode of ARF. Up to date, only prevention strategies have shown efficacy.
    Detailed Description
    Acute Rheumatic Fever is an autoimmune inflammatory post-infectious syndrome, mainly caused by type A streptococcus. It is characterized as an inadequate immune response. It may provoke carditis (which associates valvular leakages, cardiac conduction system troubles, and pericardial signs), combined with articular, skin and neurologic signs. Only carditis, prevalent in 60% of acute rheumatic diseases, may provoke valvular sequels, which define rheumatic cardiopathy. Prevalence of acute rheumatic disease (ARD) in pproximately 6 cases per 1000 children in Sub-Saharan Africa countries, whereas prevalence in developed countries is less than a case per 100 000 children, with an annual incidence of 470 000 cases and almost 230 000 deaths annually worldwide. Carditis affect between 15 and 20 million people worldwide, mostly children and young adults from low and middle-income countries. This prevalence may be underestimated. In 2007, our team conducted a study in Mozambique and Cambodia that highlighted that, through a screening based on systematic echocardiography in children from several schools, approximately 2/3 of them had asymptomatic and unknown cardiac lesions, which cannot be screened only with a clinical examination. Role of B-type lymphocytes (B cells) in auto-immune diseases physiopathology is nowadays largely accepted and justifies, in certain auto-immune diseases, the use of therapeutics that target and destroy B cells. Rituximab is a CD-20-specific monoclonal chimeric antibody, indicated to treat B lymphomas, where its efficacy and safety have changed the management of these diseases. Recently, it is thought to use Rituximab in auto-immune diseases. Antibiotherapy based on penicillin is the standard treatment of both acute rheumatic fever and its prevention. Although no anti-inflammatory treatment has proved its efficacy, with or without steroids anti-inflammatory treatments are administered in acute episode of ARF. Up to date, only prevention strategies have shown efficacy.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Rheumatic Heart Disease in Children

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 2
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantOutcomes Assessor
    Allocation
    Randomized
    Enrollment
    234 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Rituximab plus standard of care (RTX)
    Arm Type
    Experimental
    Arm Description
    Rituximab i.v of two perfusions (375 mg/m²) administered in a 14 day-interval added to a standard of care treatment
    Arm Title
    Standard of care treatment (Control)
    Arm Type
    Active Comparator
    Arm Description
    Standard of care treatment
    Intervention Type
    Drug
    Intervention Name(s)
    Rituximab added to standard of care treatment
    Intervention Description
    Rituximab with standard of care treatment
    Intervention Type
    Drug
    Intervention Name(s)
    standard of care treatment
    Intervention Description
    Standard of care treatment alone
    Primary Outcome Measure Information:
    Title
    Rheumatic valvular lesions rate
    Description
    Rheumatic valvular lesions rate, measured by echocardiography
    Time Frame
    6 months post randomization
    Secondary Outcome Measure Information:
    Title
    Incidence of rheumatic valvular lesions
    Description
    Rate of rheumatic valvular lesions will be compared between groups
    Time Frame
    14 days, 3, 6 and 12 months post-randomization
    Title
    Serious adverse events rates
    Description
    Serious adverse events rate will be compared between groups
    Time Frame
    at 14 days, 3, 6, and 12 months after randomization

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    5 Years
    Maximum Age & Unit of Time
    17 Years
    Accepts Healthy Volunteers
    No
    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

    12. IPD Sharing Statement

    Plan to Share IPD
    Undecided

    Learn more about this trial

    Rituximab in Patients With Acute Rheumatic Fever

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