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Completed

NCT Number: NCT00138736

Study on Mannan Binding Lectin (MBL) Substitution in MBL-Deficient Children With Chemotherapy-Induced Neutropenia

The pharmacokinetics, and clinical and biological effects of MBL replacement therapy in MBL-deficient children during chemotherapy-induced neutropenia were studied.

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Key information

Age range

Up to 12 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Academic Medical Centre, Amsterdam, Netherlands

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About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Children ages 0 - 12 years, during chemotherapy, and expected to become neutropenic
  • MBL deficiency by genotype or phenotype (< 100 ng/ml)
  • Informed consent and assent of patient and/or legal representative

Exclusion criteria

  • Inability or unwillingness to comply with the protocol or likely inability to complete the study period
  • Known allergic reactions to MBL and other human plasma products
  • Participation in other investigational drug studies within the last month
  • Clinically relevant abnormalities in: serum immunoglobulins IgG, IgA, IgM; blood counts; complement factors measured by AP50, CH50; urine protein and cell counts; serum creatinine and liver enzymes, as routinely determined for regular patient care.

Treatment and study plan

Mannan Binding Lectin (MBL)

Drug

Mannan Binding Lectin

Drug

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

Other names: MBL SSI

Primary outcomes

  1. pharmacokinetics of MBL

    Time frame: until the patient's absolute neutrophil count (ANC) is above 500/uL blood.

Secondary outcomes

  1. days of fever

    Time frame: until the patient's absolute neutrophil count (ANC) is above 500/uL blood.

  2. days of hospital admission

    Time frame: until the patient's absolute neutrophil count (ANC) is above 500/uL blood.

  3. use of antibiotics or antifungal medication

    Time frame: until the patient's absolute neutrophil count (ANC) is above 500/uL blood.

  4. number and type of infections

    Time frame: until the patient's absolute neutrophil count (ANC) is above 500/uL blood.

  5. MBL-dependent opsonizing capacity in vitro

    Time frame: until the patient's absolute neutrophil count (ANC) is above 500/uL blood.

  6. safety and incidence of side effects

    Time frame: until the patient's absolute neutrophil count (ANC) is above 500/uL blood.

Sponsors and collaborators

Lead sponsor

Prothya Biosolutions

Industry

Collaborators

  • Landsteiner Foundation for Blood Transfusion

Registry information

Official study title

Phase II Study on Mannan Binding Lectin (MBL) Substitution in MBL-Deficient Children With Chemotherapy-Induced Neutropenia

Important dates

Study start
2004
Study completion
2006
First posted
Aug 30, 2005
Registry last updated
Aug 30, 2007

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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