The pharmacokinetics, and clinical and biological effects of MBL replacement therapy in MBL-deficient children during chemotherapy-induced neutropenia were studied.
Mannan Binding Lectin (MBL) is a member of the lectin pathway of the complement system and plays an important role in the innate immune system. MBL replacement in MBL-deficient children with chemotherapy-induced neutropenia represents a new approach to lower the risk of febrile episodes, of hospital admission, of prolonged use of intravenous antibiotics and of severe infections. The aim of the Phase II study is to find evidence for the correct prediction of plasma levels of MBL necessary for clinical effects and biological efficacy, to confirm the dosage regimen needed to reach the required MBL plasma levels, and reconfirm the safety and lack of side-effects.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Enrollment
12
MBL dose at a twice weekly dose interval (3 or 4 days): 0.2 mg/kg, for a 3-day interval; 0.3 mg/kg, for a 4-day interval
Academic Medical Centre
Amsterdam, Netherlands
Erasmus Medical Centre
Rotterdam, Netherlands
pharmacokinetics of MBL
Time frame: until the patient's absolute neutrophil count (ANC) is above 500/uL blood.
days of fever
Time frame: until the patient's absolute neutrophil count (ANC) is above 500/uL blood.
days of hospital admission
Time frame: until the patient's absolute neutrophil count (ANC) is above 500/uL blood.
use of antibiotics or antifungal medication
Time frame: until the patient's absolute neutrophil count (ANC) is above 500/uL blood.
number and type of infections
Time frame: until the patient's absolute neutrophil count (ANC) is above 500/uL blood.
MBL-dependent opsonizing capacity in vitro
Time frame: until the patient's absolute neutrophil count (ANC) is above 500/uL blood.
safety and incidence of side effects
Time frame: until the patient's absolute neutrophil count (ANC) is above 500/uL blood.
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