Utilization and Compliance of Respiratory Syncytial Virus Monoclonal Antibody Therapy
NCT00420966 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 25003
Last updated 2018-04-17
Summary
The purpose of this study is to determine the utilization patterns and compliance rates of palivizumab, which is a monoclonal antibody therapy used to prevent respiratory syncytial virus infection.
Conditions
- Lower Respiratory Tract Infection
- Respiratory Syncytial Virus Infections
Sponsors & Collaborators
- collaborator INDUSTRY
-
Sunnybrook Health Sciences Centre
lead OTHER
Principal Investigators
-
Ian Mitchell, MB, FRCPC · University of Calgary
-
Krista L Lanctôt, PhD · Sunnybrook Health Sciences Centre
-
Bosco Paes, MD, FRCPC · McMaster University
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2005-10-31
- Primary Completion
- 2017-06-26
- Completion
- 2017-06-26
Countries
- Canada
Study Locations
More Related Trials
-
A Study to Evaluate the Safety, Reactogenicity, and Immunogenicity of Adenovirus Serotype 26 Based Respiratory Syncytial Virus Pre-fusion (Ad26.RSV.Pre-F) Vaccine in RSV-Seronegative Toddlers 12 to 24 Months of Age
NCT03606512 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
Study of Motavizumab (MEDI-524) and Palivizumab Administered Sequentially in the Same Respiratory Syncytial Virus (RSV) Season
NCT00316264 ·Status: COMPLETED ·Phase: PHASE2
-
A Phase 1/2/3 Study to Evaluate the Safety, Tolerability, and Immunogenicity of an RNA Vaccine Candidate Against COVID-19 in Healthy Children
NCT04816643 ·Status: COMPLETED ·Phase: PHASE2/PHASE3
-
Study of MEDI-524 (Motavizumab) for the Prophylaxis of Serious Respiratory Syncytial Virus (RSV) Disease in High-Risk Children
NCT00129766 ·Status: COMPLETED ·Phase: PHASE3
-
Respiratory Syncytial Virus (RSV) Investigational Vaccine in Infants Aged 6 and 7 Months Likely to be Unexposed to RSV
NCT03636906 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
A Study to Evaluate MEDI-524 In Children With Hemodynamically Significant Congenital Heart Disease
NCT00538785 ·Status: COMPLETED ·Phase: PHASE2
-
A Study to Evaluate the Antiviral Activity, Clinical Outcomes, Safety, Tolerability, and Pharmacokinetics of Orally Administered Lumicitabine (JNJ-64041575) Regimens in Hospitalized Infants and Children Aged 28 Days to 36 Months Infected With Respiratory Syncytial Virus
NCT03333317 ·Status: TERMINATED ·Phase: PHASE2
-
Evaluation of the Effect of Nirsevimab on Hospitalizations Due to RSV Infection in Infants Under One Year of Age.
NCT06856967 ·Status: RECRUITING
-
Immunogenicity, Safety and Tolerability of a Neisseria Meningitidis Serogroup B Bivalent Recominant Lipoprotein 2086 Vaccine (Bivalent rLP2086) in Healthy Toddlers.
NCT02534935 ·Status: COMPLETED ·Phase: PHASE2
-
Empirical Treatment Against Cytomegalovirus and Tuberculosis in HIV-infected Infants With Severe Pneumonia
NCT03915366 ·Status: COMPLETED ·Phase: PHASE2/PHASE3
-
Safety and Immunogenicity Evaluation After One or Two Doses of Novartis Meningococcal ACWY Conjugate Vaccine in Healthy Infants and Toddlers
NCT00667602 ·Status: COMPLETED ·Phase: PHASE3
-
A Study to Learn About BNT162b2 (LP.8.1)-Adapted Vaccine Against SARS-CoV-2 in Children 5 Through 11 Years of Age That Are Considered at Higher Risk of Severe COVID-19
NCT07222384 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE3
-
A Study of mRNA-1345 Vaccine Targeting Respiratory Syncytial Virus in Pregnant Women and in Infants Born to Vaccinated Mothers
NCT06143046 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE2
-
A Study to Evaluate Safety and Immune Response of Novartis Meningococcal ACWY Vaccine In Infants
NCT00474526 ·Status: COMPLETED ·Phase: PHASE3
-
Safety And Blood Collection Study Of Meningococcal B Rlp2086 Vaccine In Adults
NCT00780806 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
Safety, Tolerability and Immunogenicity of Two Different Formulations of Meningococcal B Recombinant Vaccine, When Administered to Healthy Infants
NCT00433914 ·Status: COMPLETED ·Phase: PHASE2
-
A Study to Evaluate Safety and Effectiveness of mRNA-1273 COVID-19 Vaccine in Healthy Children Between 6 Months of Age and Less Than 12 Years of Age
NCT04796896 ·Status: COMPLETED ·Phase: PHASE2/PHASE3
-
Evaluating the Infectivity, Safety and Immunogenicity of a Recombinant Live-Attenuated Respiratory Syncytial Virus Vaccine (RSV LID cp ΔM2-2) in RSV-Seronegative Infants 6 to 24 Months of Age
NCT02890381 ·Status: TERMINATED ·Phase: PHASE1
-
Study Evaluating Safety, Tolerability, and Immunogenicity of Meningococcal B Vaccine in Healthy Infants
NCT00798304 ·Status: TERMINATED ·Phase: PHASE2
-
Safety, Tolerability and Immunogenicity of Meningococcal B Recombinant Vaccine Administered With or Without Routine Infant Vaccinations to Healthy Infants According to Different Immunization Schedules
NCT00721396 ·Status: COMPLETED ·Phase: PHASE2
-
A Study to Describe the Immunogenicity, Safety, and Tolerability of Neisseria Meningitidis Serogroup B Bivalent Recombinant Lipoprotein 2086 Vaccine (Bivalent rLP2086) in Healthy Subjects Aged ≥24 Months to <10 Years
NCT02531698 ·Status: COMPLETED ·Phase: PHASE2
-
A Clinical Trial to Assess the Safety, Tolerability and Immunogenicity of MenABCWY in Healthy Infants
NCT04645966 ·Status: TERMINATED ·Phase: PHASE2
-
Study of the Safety and Immune Response of a Meningococcal Vaccine Administered to Healthy Infants
NCT00262002 ·Status: COMPLETED ·Phase: PHASE2
-
Study Evaluating Safety And Tolerability Of Meningococcal B Rlp2086 Vaccine In Healthy Adults
NCT00879814 ·Status: COMPLETED ·Phase: PHASE1
-
Safety and Immunogenicity Study of Live Attenuated Mumps Vaccines in Healthy Infants
NCT02692599 ·Status: COMPLETED ·Phase: PHASE3