SAFETY AND ANTIVIRAL ACTIVITY OF MOTAVIZUMAB, A RESPIRATORY SYNCYTIAL VIRUS (RSV)-SPECIFIC HUMANIZED MONOCLONAL ANTIBODY, WHEN ADMINISTERED TO RSV-INFECTED CHILDREN
被引:47
作者:
Lagos, Rosanna
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Ctr Para Vacunas En Desarrollo Chile, Santiago, ChileMedImmune LLC, Gaithersburg, MD 20878 USA
Lagos, Rosanna
[3
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DeVincenzo, John P.
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Univ Tennessee, Childrens Fdn Res Ctr, Sch Med, Memphis, TN USAMedImmune LLC, Gaithersburg, MD 20878 USA
DeVincenzo, John P.
[2
]
Munoz, Alma
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Ctr Para Vacunas En Desarrollo Chile, Santiago, ChileMedImmune LLC, Gaithersburg, MD 20878 USA
Previously healthy children hospitalized with respiratory syncytial virus (RSV) received motavizumab (3, 15, or 30 mg/kg intravenously), an RSV-specific monoclonal antibody, or placebo. Safety, tolerability, motavizumab concentrations, and immunogenicity were assessed. Cultivatable RSV in the upper respiratory tract was significantly reduced with motavizumab compared with placebo day 1 post-treatment. No adverse events were considered motavizumab-related by site investigators.