Double-Blind, Placebo-Controlled Study of Bezlotoxumab in Children Receiving Antibacterial Treatment for Clostridioides difficile Infection (MODIFY III)
Jazyk angličtina Země Velká Británie, Anglie Médium print
Typ dokumentu randomizované kontrolované studie, multicentrická studie, časopisecké články
Grantová podpora
Merck Sharp & Dohme
PubMed
37389891
PubMed Central
PMC10312293
DOI
10.1093/jpids/piad031
PII: 7213927
Knihovny.cz E-zdroje
- Klíčová slova
- Clostridioides difficile infection, adolescents, bezlotoxumab, children, recurrence,
- MeSH
- antibakteriální látky * terapeutické užití MeSH
- dítě MeSH
- dospělí MeSH
- dvojitá slepá metoda MeSH
- klostridiové infekce * farmakoterapie MeSH
- lidé MeSH
- monoklonální protilátky terapeutické užití MeSH
- Check Tag
- dítě MeSH
- dospělí MeSH
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- multicentrická studie MeSH
- randomizované kontrolované studie MeSH
- Názvy látek
- antibakteriální látky * MeSH
- bezlotoxumab MeSH Prohlížeč
- monoklonální protilátky MeSH
BACKGROUND: Therapies to prevent recurrence of Clostridioides difficile infection (CDI) in pediatric patients are needed. Bezlotoxumab is a fully human monoclonal antibody approved for prevention of recurrent CDI in adults. We assessed the pharmacokinetics, safety, tolerability, and efficacy of bezlotoxumab in pediatric patients. METHODS: MODIFY III was a multicenter, double-blind, placebo-controlled study of bezlotoxumab in children (1 to <18 years) receiving antibacterial treatment for CDI. Participants were randomized 3:1 to receive a single infusion of bezlotoxumab (10 mg/kg) or placebo and were stratified by age at randomization (cohort 1: 12 to <18 years, cohort 2: 1 to <12 years). The primary objective was to characterize bezlotoxumab pharmacokinetics to support dose selection for pediatric patients; the primary endpoint was the area under the bezlotoxumab serum concentration-time curve (AUC0-inf). Safety, tolerability, and efficacy were monitored for 12 weeks post-infusion. RESULTS: A total of 148 participants were randomized and 143 were treated: 107 with bezlotoxumab and 36 with placebo (cohort 1 n = 60, cohort 2 n = 83; median age 9.0 years); 52.4% of participants were male and 80.4% were white. Geometric mean ratios (90% CI) for bezlotoxumab AUC0-inf were 1.06 (0.95, 1.18) and 0.82 (0.75, 0.89) h * μg/mL for cohorts 1 and 2, respectively. Bezlotoxumab 10 mg/kg was generally well-tolerated with an adverse event profile similar to placebo, including no treatment discontinuations due to adverse events. CDI recurrence was low and comparable for bezlotoxumab (11.2%) and placebo (14.7%). CONCLUSIONS: The results of this study support the bezlotoxumab dose of 10 mg/kg for pediatric patients. TRIAL REGISTRATION: NCT03182907 at ClinicalTrials.gov.
Biostatistics Merck and Co Inc Rahway New Jersey USA
Clinical Operations Merck and Co Inc Rahway New Jersey USA
Clinical Research MSD UK London UK
Department of Pediatric Oncology University Hospital Brno Brno Czech Republic
Division of Infectious Diseases Children's Hospital Los Angeles Los Angeles California USA
Pediatric Hematology Oncology Department Hospital Niño Jesus Madrid Spain
doi: 10.1093/jpids/piad025 PubMed
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ClinicalTrials.gov
NCT03182907