The primary goal was to describe the safety of the investigational product when given monthly to prevent serious respiratory infection among children with significant heart disease.
The primary objective was to describe the safety and tolerability of motavizumab when given monthly as prophylaxis against serious RSV infection among children with hemodynamically significant congenital heart disease.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
QUADRUPLE
Enrollment
1,236
15 mg/kg IM administered at monthly intervals
15 mg/kg IM administered at monthly intervals
Number of Subjects Reporting Adverse Events Through Study Day 150
Adverse events were summarized by system organ class (SOC) and preferred term (using MedDRA Version 11.1) overall.
Time frame: Days 0-150
Number of Subjects Reporting Serious Adverse Events Through Study Day 150
Serious adverse events were those that resulted in death; were life-threatening; resulted in subject hospitalization or prolongation of existing hospitalization; resulted in persistent or significant disability or incapacity; or were an important medical event that may not have resulted in death, threatened life, or required hospitalization and that, based on appropriate medical judgment, may have jeopardized the subject and may have required medical or surgical intervention to prevent one of the outcomes listed above.
Time frame: Days 0-150
Number of Subjects Reporting Laboratory Adverse Events
Time frame: Days 0-150
The Number of Subjects Hospitalized for RSV Infection.
An RSV hospitalization was defined as one of the following: 1) Cardiac/respiratory hospitalization with a positive real-time RT-PCR RSV diagnostic test performed at a central laboratory, or 2) New onset of lower respiratory tract symptoms with an objective measure of worsening respiratory status in an already hospitalized subject with a positive real-time RT-PCR RSV diagnostic test performed at a central laboratory (nosocomial RSV hospitalization), or 3) Death demonstrated to be caused by RSV (based on virologic evidence and either clinical history or autopsy).
Time frame: Days 0-150
The Number of Subjects With RSV Outpatient MA-LRI for Season 2 Only.
An RSV outpatient MA-LRI was defined as an outpatient medically-attended event designated by the principal investigator as a lower respiratory illness with a positive real-time RT-PCR RSV diagnostic test performed at a central laboratory.
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Arkansas Pediatric Clinic
Little Rock, Arkansas, United States
Miller Children's Hospital
Long Beach, California, United States
Childrens Hospital Los Angeles
Los Angeles, California, United States
Children's Hospital and Research Center at Oakland
Oakland, California, United States
University of California Davis Medical Center
Sacramento, California, United States
Children's Hospital And Health Center
San Diego, California, United States
Yale New Haven Children's Hospital
New Haven, Connecticut, United States
Children's National Medical Center
Washington D.C., District of Columbia, United States
Nemours Children's Clinic Biomedical Research Department
Orlando, Florida, United States
James Whitcomb Riley Hospital for Children
Indianapolis, Indiana, United States
...and 142 more locations
Time frame: Days 0-150
Number of Subjects Who Had Anti-motavizumab Antibodies Detected
ECLA-based method
Time frame: Days 0-150
Mean Trough Serum Concentration of Motavizumab at Pre-dose 1
Trough serum concentrations (ug/mL) of motavizumab at pre-dose 1
Time frame: Pre-dose 1
Mean Trough Serum Concentration of Motavizumab at 30 Days Post-dose 1
Trough serum concentrations (ug/mL) of motavizumab at 30 days post-dose 1
Time frame: 30 days post-dose 1
Mean Trough Serum Concentration of Motavizumab at 30 Days Post-dose 2
Trough serum concentrations (ug/mL) of motavizumab at 30 days post-dose 2
Time frame: 30 days post-dose 2
Mean Trough Serum Concentration of Motavizumab at 30 Days Post-dose 3
Trough serum concentrations (ug/mL) of motavizumab at 30 days post-dose 3
Time frame: 30 days post-dose 3
Mean Trough Serum Concentration of Motavizumab at 30 Days Post-dose 4
Trough serum concentrations (ug/mL) of motavizumab at 30 days post-dose 4
Time frame: 30 days post-dose 4
Mean Trough Serum Concentrations of Motavizumab in Subjects Who Underwent Cardiac Surgery With Cardiopulmonary Bypass
Subjects who underwent cardiac surgery with cardiopulmonary bypass through Study Day 150 were to have a blood sample taken for determination of study drug concentrations prior to receipt of another dose of study drug immediately following surgery.
Time frame: Days 0-150