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"Palivizumab Therapy for RSV-bronchiolitis"

Primary Purpose

Respiratory Syncytial Virus-bronchiolitis

Status
Completed
Phase
Phase 3
Locations
Qatar
Study Type
Interventional
Intervention
Palivizumab
Placebo
Sponsored by
Hamad Medical Corporation
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Respiratory Syncytial Virus-bronchiolitis focused on measuring Respiratory syncytial virus, Palivizumab, Bronchiolitis, Treatment

Eligibility Criteria

undefined - 3 Months (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Infants ≤ 3 months-old, presenting to the main pediatric ER with acute bronchiolitis associated with positive RSV rapid antigen test.

Exclusion Criteria:

  • Patients will be excluded from the study if they had 1 or more of the following characteristics:

    • Received monoclonal antibody or IVIG within the last 3 months prior to randomization.
    • Receipt of steroids within 2 days before randomization.
    • Hypersensitivity to monoclonal antibodies or immunoglobulin products.
    • Immunodeficiency.
    • Suspected sepsis.
    • Seizure disorders.
    • Neuromuscular disorders.
    • Congenital heart disease.
    • Major congenital anomalies of respiratory tract.

Sites / Locations

  • Hamad Medical Corporation

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Palivizumab

Placebo

Arm Description

A single dose of IV palivizumab

An equivalent volume of 0.9% normal saline.

Outcomes

Primary Outcome Measures

Readmission to either infirmary/observation or hospital or PICU during 3 weeks of follow-up after discharge

Secondary Outcome Measures

Time to medical readiness for discharge
Revisit to any medical facility for the same illness
Admission to PICU during initial admission

Full Information

First Posted
May 10, 2015
Last Updated
February 26, 2018
Sponsor
Hamad Medical Corporation
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1. Study Identification

Unique Protocol Identification Number
NCT02442427
Brief Title
"Palivizumab Therapy for RSV-bronchiolitis"
Official Title
Treatment of Respiratory Syncytial Virus Bronchiolitis in Young Infants With Humanized Monoclonal Antibody: A Randomized Clinical Trial (Palivizumab Study)
Study Type
Interventional

2. Study Status

Record Verification Date
January 2018
Overall Recruitment Status
Completed
Study Start Date
September 2014 (undefined)
Primary Completion Date
February 1, 2018 (Actual)
Study Completion Date
February 1, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hamad Medical Corporation

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
There is a growing body of literature suggesting that monoclonal antibody could be efficacious in infants with RSV-bronchiolitis, well tolerated with no or clinically insignificant adverse effects. "The investigators hypothesize that a single dose of iv palivizumab 15 mg/kg in diagnosed infants <3 months old with RSV bronchiolitis will result in fewer infants with readmissions to infirmary/observation or hospital for relapse during 3 weeks of follow-up after discharge".
Detailed Description
Setting: The study will be conducted between September 2014 and April 2018 in the short stay unit of the Pediatric Emergency Center (PEC) of Hamad General Hospital, the only pediatric emergency facility in the State of Qatar. The PEC serves an average of 280 000 patients annually and manages 42 beds in a short stay infirmary unit, to which patients are admitted if they are too ill to be sent home but do not need the intensive care unit. Patients admitted to the unit are assessed at least every 6 hours by a pediatrician to determine readiness for discharge. The length of stay in the unit for bronchiolitis ranges from 6 to 168 hours. In 2012, the investigators saw 8718 infants and young children in 10 666 visits for bronchiolitis. Infants aged ≤3 months presenting to the unit for treatment of viral bronchiolitis will be eligible for the study. Consecutive patients will be recruited except when a study nurse is unavailable or the unit is too busy to recruit. Procedure: Patients will be examined on presentation, and those needing additional treatment or observation will be admitted to the short stay infirmary unit. Consecutive patients with bronchiolitis will be assessed for study eligibility within 2 hours. Eligible patients will be enrolled after obtaining written consent. For those who consent, plain chest radiography, and nasopharyngeal swabs will be taken for RSV detection. If the patient has a positive RSV rapid antigen test, patients will be randomized to receive one of the study arms. Bronchiolitis severity score will be measured initially at the start of treatment and then at 12-hour, 24-hour, 36-hour and 48-hour thereafter. The medical team in addition to the parents and patients will be blinded to the medication delivered. Adverse effects in each group will be carefully monitored and documented. Patients will be sent home with salbutamol metered-dose inhalers with an appropriately sized Aerochamber with mask attachment. Daily follow-up by study nurse by telephone is mandatory for 1 week after discharge and then once a week for 2 weeks thereafter. The patient could return to the pediatric emergency center earlier if needed. At all revisits for the same illness, nasopharyngeal swabs will be taken for RSV rapid antigen test and the result recorded. Study Intervention: Active arm: A single dose of IV palivizumab 15 mg per kilogram body weight (maximum dose =100 mg). Control arm: Placebo (an equivalent volume of 0.9% normal saline).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Respiratory Syncytial Virus-bronchiolitis
Keywords
Respiratory syncytial virus, Palivizumab, Bronchiolitis, Treatment

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
420 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Palivizumab
Arm Type
Active Comparator
Arm Description
A single dose of IV palivizumab
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
An equivalent volume of 0.9% normal saline.
Intervention Type
Drug
Intervention Name(s)
Palivizumab
Other Intervention Name(s)
Monoclonal antibody
Intervention Description
A single dose of IV palivizumab 15 mg per kilogram body weight (maximum dose =100 mg). The study medication will be given by IV infusion over 30 minutes using a syringe infusion pump.
Intervention Type
Other
Intervention Name(s)
Placebo
Other Intervention Name(s)
0.9% Normal saline
Intervention Description
An equal volume of 0.9% normal saline
Primary Outcome Measure Information:
Title
Readmission to either infirmary/observation or hospital or PICU during 3 weeks of follow-up after discharge
Time Frame
3 weeks
Secondary Outcome Measure Information:
Title
Time to medical readiness for discharge
Time Frame
4 weeks
Title
Revisit to any medical facility for the same illness
Time Frame
4 weeks
Title
Admission to PICU during initial admission
Time Frame
4 weeks

10. Eligibility

Sex
All
Maximum Age & Unit of Time
3 Months
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Infants ≤ 3 months-old, presenting to the main pediatric ER with acute bronchiolitis associated with positive RSV rapid antigen test. Exclusion Criteria: Patients will be excluded from the study if they had 1 or more of the following characteristics: Received monoclonal antibody or IVIG within the last 3 months prior to randomization. Receipt of steroids within 2 days before randomization. Hypersensitivity to monoclonal antibodies or immunoglobulin products. Immunodeficiency. Suspected sepsis. Seizure disorders. Neuromuscular disorders. Congenital heart disease. Major congenital anomalies of respiratory tract.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dr. Khalid Alansari
Organizational Affiliation
Hamad Medical Corporation, Doha, Qatar
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hamad Medical Corporation
City
Doha
ZIP/Postal Code
3050
Country
Qatar

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
30760509
Citation
Alansari K, Toaimah FH, Almatar DH, El Tatawy LA, Davidson BL, Qusad MIM. Monoclonal Antibody Treatment of RSV Bronchiolitis in Young Infants: A Randomized Trial. Pediatrics. 2019 Mar;143(3):e20182308. doi: 10.1542/peds.2018-2308. Epub 2019 Feb 13.
Results Reference
derived

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"Palivizumab Therapy for RSV-bronchiolitis"

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