A Trial Comparing the Efficacy and Safety of Anakinra Versus Intravenous Immunoglobulin (IVIG) Retreatment, in Patients With Kawasaki Disease Who Failed to Respond to Initial Standard IVIG Treatment — ANACOMP  

Kawasaki Disease Clinical Trial

Official title: A Randomized Phase III Multicenter Trial Comparing the Efficacy and Safety of Anakinra Versus Intravenous Immunoglobulin (IVIG) Retreatment, in Patients With Kawasaki Disease Who Failed to Respond to Initial Standard IVIG Treatment

Status Recruiting

Clinical Trial Summary

Kawasaki disease (KD) is the most frequent vasculitis in younger children <5years, and the first cause of acquired ischemic myocardiopathy in childhood. Exceptionally, KD may cause early death during the acute phase by myocardial infarction, but may compromise the long-term cardiovascular outcome by accelerating atherosclerotic disease.

The incidence of KD is high in far-Eastern countries and Hawaii but KD is relatively rare in other regions (10/100000 children <5years in northern Europe) which makes it difficult to develop research on these rare population.

Early recognition and treatment by intravenous immunoglobulins (IVIG) influences the prognosis positively. IVIG are the standard of care and decrease significantly the risk of coronary aneurysms. However, despite a first infusion of IVIG, 20% of KD patients remain febrile and have high risk of coronary vasculitis. Recent Japanese research group assessed additional cyclosporine treatment in first line KD treatment but failed preventing relapse. To date there is no agreement for a more effective second line treatment.

Based on the auto-inflammatory pattern of KD, the investigators hypothesize that anti IL-1 blocking agents could bring a rapid and sustained effect on systemic and coronary inflammation in patients with KD.

Our hypotheses are:

1. Anakinra treatment may reduce the early and long-term mortality of patients with Kawasaki Disease (KD), by a rapid and sustained effect on vascular inflammation.

2. The safety of anakinra is good, as the drug has a very short half-life, which allows its rapid withdrawal in case of serious adverse event.

The use of anakinra is not associated with the risk of contamination by infectious agents, which remain even minimal, a possibility with the use of IVIG.

Clinical Trial Description

It is a multicentric national randomized controlled, parallel-group in a 1:1 ratio, open labelled trial of superiority.

The main objective is to compare the efficacy of Anakinra (Interleukin 1 receptor type 1 - receptor antagonist) with 2nd IVIG infusion, in second line, on fever in patients with KD, who failed to respond to one infusion of IVIG(standard treatment).

The main criterion-evaluating efficacy in both groups is: the patient must reach a body (axillary (+0.5°C), tympanic, oral) temperature <38˚C within 2 days after initiation of treatment (i.e. a binary outcome: success/failure).

The secondary objectives are to compare Anakinra with IVIG retreatment in terms of:

• Efficacy on fever at 72h

• Efficacy on disease activity

• Efficacy on KD symptoms

• Efficacy on coronary lesions (e.g.: dilatation and aneurysm)

• Efficacy on inflammation

• Safety and tolerability Secondary End Points (linked with the secondary objectives)

To compare Anakinra with IVIG retreatment in terms of:

• Temperature <38˚C within 3 days (72h) after initiation of treatment

• Decrease of the CRP values from baseline to day 30(CRP<6 mg/L at day 30)

• Reduction in physician assessment of disease activity, on a 10 points scale, of at least to 50% between baseline and day 14.

• Reduction in patient's parent's assessment of disease activity, on a 10 points scale, of to at least 50% between baseline and day 14.

• Resolution of coronary abnormalities; i.e worst Z score <2.5, by echocardiogram if present at day 45.

• Adverse events: pain/redness at injection site, bacterial infection hepatitis, macrophage activation syndrome, severe neutropenia,

• Monitoring of adverse events

• Physical examination: Complete clinical exam will be performed at each visit to detect symptoms of KD (rash, cervical nodes, mucous lesions, extremities, GI, pulmonary, cardio vascular, neurologic and muscular/joint evaluation) and possible associated morbidity: e.g. concomitant infection

• Local tolerability of injections: will be evaluated by physician from V2 to V8:

pain, redness, swelling, induration, itching, haemorrhage, (and quoted from none, mild, moderate, severe)

• Vital signs and body measurements: at each visit: V1 to V9. The body temperature will be measured daily until d30. Parents will receive a follow-up booklet..

• Laboratory evaluations: hematologic, hepatic and renal assessment will be followed

Group 1: KINERET:

KINERET® in the form of prefilled syringe with 100 mg of anakinra per 0.67 ml (150 mg/mL) and adapted to paediatric population, in pack sizes of 7. Patients in group I, will receive a starting dose of anakinra is 4 mg/kg at visit D1 (or day 0, if possible). During visits D1 and D2, if patients are still febrile with 12 hours (H12) of treatment, they will receive a supplementary dose of 2 mg/Kg; otherwise, they will remain at a starting dose of 4mg/kg. If they are still febrile at H24, they will receive a dose of 8mg/kg; otherwise, they will maintain their dose of 6 mg/kg. Patients with temperature <38°C at any point between initiation and day 14, but who develop secondary fever due to KD could have further escalation dose of anakinra until a maximum dose of 8mg/Kg.

Group 2: IVIG Immunoglobulins concentrates used for the ANACOMP study should be preferably the specialty PRIVIGEN® 100mg/mL (=10g of human immunoglobulins) solute for intravenous infusion, manufactured by CSL Behring (Commonwealth Serum Laboratories). Other presentations in mL (25, 50, 200, 400 exist corresponding to respectively 2.5g, 5g, 20, and 40g of immunoglobulins). Patients in group II, will receive one infusion of 2g/kg of intravenous Immunoglobulins at visit D1 (or day 0, if possible) ;

Related Conditions & MeSH terms

• Kawasaki Disease
• Mucocutaneous Lymph Node Syndrome

• NCT number: NCT04656184
• Study type: Interventional
• Source: Assistance Publique - Hôpitaux de Paris
• Contact: Isabelle Koné-Paut, Pr
• Phone: 00 33 1 45 21 32 46
• Email: isabelle.kone-paut@aphp.fr
• Status: Recruiting
• Phase: Phase 3
• Start date: October 20, 2023
• Completion date: March 2027