• Pediatr. Infect. Dis. J. · Jul 2014

    Randomized Controlled Trial Multicenter Study

    Motavizumab treatment of infants hospitalized with respiratory syncytial virus infection does not decrease viral load or severity of illness.

    • Octavio Ramilo, Rosanna Lagos, Xavier Sáez-Llorens, JoAnn Suzich, C Kathy Wang, Kathryn M Jensen, Brian S Harris, Genevieve A Losonsky, M Pamela Griffin, and Motavizumab Study Group.
    • From the *Nationwide Children's Hospital, Ohio State University College of Medicine, Columbus, OH; †Centro Para Vacunas En Desarrollo-Chile, Santiago, Chile; ‡Hospital del Niño, Ciudad de Panamá, Panamá; and §MedImmune, Gaithersburg, MD.
    • Pediatr. Infect. Dis. J. 2014 Jul 1; 33 (7): 703-9.

    BackgroundThis study was conducted to determine whether treatment with motavizumab, an anti-respiratory syncytial virus (RSV) monoclonal antibody, would decrease viral load and improve clinical outcomes in previously healthy term infants hospitalized with RSV lower respiratory tract infection.MethodsInfants hospitalized with lower respiratory tract infection and a positive RSV test performed locally were randomized to receive 1 intravenous dose of motavizumab (30 or 100 mg/kg) or placebo. Nasal wash samples were tested by real-time reverse transcriptase polymerase chain reaction at a central laboratory to determine viral load. Clinical data were collected during RSV hospitalization and at 12-month follow up.ResultsOf 118 infants, 112 were confirmed RSV positive by real-time reverse transcriptase polymerase chain reaction. In each study group, median (range) RSV load (log10 copies/mL) decreased at a similar rate from baseline to study day 7 [motavizumab 30 mg/kg: 8.35 (2.5-9.5) to 5.03 (2.5-6.8); motavizumab 100 mg/kg: 8.22 (5.5-9.7) to 4.25 (2.5-8.0); placebo: 8.02 (6.7-9.8) to 5.17 (2.5-7.3)]. Median (range) duration of hospitalization was 3.05 (0.8-16.0), 2.99 (1.0-25.0) and 2.88 (0.8-11.7) days for the motavizumab 30 mg/kg, motavizumab 100 mg/kg and placebo groups, respectively. Six (8%) motavizumab and 0 placebo recipients were admitted to the intensive care unit and 4 required mechanical ventilation. The incidence of wheezing episodes during the 12-month follow up was comparable for all 3 groups.ConclusionsMotavizumab had no appreciable effect on RSV viral load measured in the upper respiratory tract of children hospitalized for RSV lower respiratory tract infection. No differences were observed for duration of hospitalization, severity of illness measures or wheezing episodes during 12-month follow up in children treated with motavizumab or placebo.

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