search
Back to results

Preventing Asthma in High Risk Kids (PARK)

Primary Purpose

Asthma

Status
Recruiting
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Omalizumab
Placebo
Sponsored by
Boston Children's Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Asthma

Eligibility Criteria

24 Months - 47 Months (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Parent/guardian must be able to understand and provide signed and dated written informed consent; he/she must also be able to communicate with study staff.
  2. 24-47 months of age at randomization
  3. 2-4 wheezing episodes in the past year
  4. positive allergy to aeroallergen
  5. first degree relative with history or current diagnosis of asthma or allergy
  6. If is participating in a food immunotherapy treatment that is not part of a clinical trial, has been on an established maintenance regimen implemented continuously for a minimum of 2 months.

Exclusion Criteria:

  1. >4 episodes of wheezing in the past year
  2. Use of Step 5 or Step 6 therapy (ICS plus LABA ) at the time of enrollment (Visit 0).
  3. Need for systemic corticosteroids or a hospitalization for respiratory symptoms within four weeks prior to screening.
  4. Three or more courses of systemic corticosteroids for wheezing illnesses in the last year
  5. More than four days of symptoms of wheezing, or tightness in the chest or cough in the past two weeks causing at least minimal limitation of activity
  6. More than four days of albuterol treatment (for symptoms) in the past two weeks
  7. More than one night of symptoms of wheezing, or tightness in the chest or cough causing sleep disruption in the past two weeks
  8. More than one night of albuterol treatment (for symptoms) in the past two weeks
  9. Prematurity (<34 weeks gestation)
  10. Need for oxygen for more than 5 days in the neonatal period
  11. History of intubation or mechanical ventilation for respiratory illness
  12. Other significant medical conditions, including: major congenital anomalies, cystic fibrosis, chronic pulmonary diseases, bronchopulmonary dysplasia, thoracic surgery, history of tuberculosis, immunodeficiency (primary or secondary), seizure disorders
  13. Expecting to relocate within 4 years of study initiation to a place which would make in-person clinical visits impossible
  14. Deemed unable to adhere to study activities
  15. Prior aeroallergen immunotherapy or use of biologics including anti-IgE
  16. Prior IVIG or systemic immunosuppressant other than corticosteroids
  17. History of hypoxic seizures during a wheezing episode
  18. Total IgE outside of the omalizumab dosing range.
  19. Enrolled in any clinical medication trial within the past 30 days.
  20. With platelet counts < 150 x 109/L at the Screening Visit (V0)
  21. Past or current medical problems or findings from physical examination or laboratory testing that are not listed above, which, in the opinion of the investigator, may pose additional risks from participation in the study, may interfere with the participant's ability to comply with study requirements or may impact the quality or interpretation of the data obtained from the study.
  22. History of severe anaphylactic/anaphylactoid reactions from any cause

Sites / Locations

  • Phoenix Children's HospitalRecruiting
  • Rady Children's Hospital - San DiegoRecruiting
  • Childrens Hospital ColoradoRecruiting
  • Connecticut Children's HospitalRecruiting
  • Children's National Medical CenterRecruiting
  • Emory UniversityRecruiting
  • Ann & Robert H. Lurie Children's Hospital of ChicagoRecruiting
  • Indiana University/Riley Children's HospitalRecruiting
  • Boston Children's HospitalRecruiting
  • Washington UniversityRecruiting
  • Cincinnati Children's Hospital Medical CenterRecruiting
  • Texas Children's Hospital/Baylor College of MedicineRecruiting
  • University of WisconsinRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Active

Placebo

Arm Description

omalizumab 0.016 mg/kg/IU total IgE

looks like active drug

Outcomes

Primary Outcome Measures

active asthma diagnosis
questionnaire
asthma severity
questionnaire

Secondary Outcome Measures

number of positive new allergic sensitization
skin prick test
decrease in number of wheezing episodes
questionnaires

Full Information

First Posted
July 28, 2015
Last Updated
February 6, 2023
Sponsor
Boston Children's Hospital
Collaborators
National Institute of Allergy and Infectious Diseases (NIAID)
search

1. Study Identification

Unique Protocol Identification Number
NCT02570984
Brief Title
Preventing Asthma in High Risk Kids
Acronym
PARK
Official Title
Controlling and Preventing Asthma Progression and Severity in Kids
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Recruiting
Study Start Date
November 27, 2018 (Actual)
Primary Completion Date
November 27, 2025 (Anticipated)
Study Completion Date
November 27, 2027 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Boston Children's Hospital
Collaborators
National Institute of Allergy and Infectious Diseases (NIAID)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This trial is a randomized, double-blind, placebo controlled trial designed to test whether two years treatment of preschool children aged 2-3 years of age at high risk for asthma with omalizumab (anti-IgE) for two years will prevent the progression to childhood asthma, as reflected by a reduction in the prevalence of active asthma in the Final 12 months during 2 year observation period off study drug.
Detailed Description
Prevention/ Disease modification of asthma.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Asthma

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
200 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Active
Arm Type
Active Comparator
Arm Description
omalizumab 0.016 mg/kg/IU total IgE
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
looks like active drug
Intervention Type
Drug
Intervention Name(s)
Omalizumab
Other Intervention Name(s)
Xolair
Intervention Description
anti-ige injection
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
placebo arm
Intervention Description
placebo comparator arm, injection similar to active
Primary Outcome Measure Information:
Title
active asthma diagnosis
Description
questionnaire
Time Frame
Final 12 months during 2 year observation period off study drug
Title
asthma severity
Description
questionnaire
Time Frame
Final 12 months during 2 year observation period off study drug
Secondary Outcome Measure Information:
Title
number of positive new allergic sensitization
Description
skin prick test
Time Frame
Final 12 months during 2 year observation period off study drug
Title
decrease in number of wheezing episodes
Description
questionnaires
Time Frame
Final 12 months during 2 year observation period off study drug

10. Eligibility

Sex
All
Minimum Age & Unit of Time
24 Months
Maximum Age & Unit of Time
47 Months
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Parent/guardian must be able to understand and provide signed and dated written informed consent; he/she must also be able to communicate with study staff. 24-47 months of age at randomization 2-4 wheezing episodes in the past year positive allergy to aeroallergen first degree relative with history or current diagnosis of asthma or allergy If is participating in a food immunotherapy treatment that is not part of a clinical trial, has been on an established maintenance regimen implemented continuously for a minimum of 2 months. Exclusion Criteria: >4 episodes of wheezing in the past year Use of Step 5 or Step 6 therapy (ICS plus LABA ) at the time of enrollment (Visit 0). Need for systemic corticosteroids or a hospitalization for respiratory symptoms within four weeks prior to screening. Three or more courses of systemic corticosteroids for wheezing illnesses in the last year More than four days of symptoms of wheezing, or tightness in the chest or cough in the past two weeks causing at least minimal limitation of activity More than four days of albuterol treatment (for symptoms) in the past two weeks More than one night of symptoms of wheezing, or tightness in the chest or cough causing sleep disruption in the past two weeks More than one night of albuterol treatment (for symptoms) in the past two weeks Prematurity (<34 weeks gestation) Need for oxygen for more than 5 days in the neonatal period History of intubation or mechanical ventilation for respiratory illness Other significant medical conditions, including: major congenital anomalies, cystic fibrosis, chronic pulmonary diseases, bronchopulmonary dysplasia, thoracic surgery, history of tuberculosis, immunodeficiency (primary or secondary), seizure disorders Expecting to relocate within 4 years of study initiation to a place which would make in-person clinical visits impossible Deemed unable to adhere to study activities Prior aeroallergen immunotherapy or use of biologics including anti-IgE Prior IVIG or systemic immunosuppressant other than corticosteroids History of hypoxic seizures during a wheezing episode Total IgE outside of the omalizumab dosing range. Enrolled in any clinical medication trial within the past 30 days. With platelet counts < 150 x 109/L at the Screening Visit (V0) Past or current medical problems or findings from physical examination or laboratory testing that are not listed above, which, in the opinion of the investigator, may pose additional risks from participation in the study, may interfere with the participant's ability to comply with study requirements or may impact the quality or interpretation of the data obtained from the study. History of severe anaphylactic/anaphylactoid reactions from any cause
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Wanda Phipatanakul, MD, MS
Phone
857-218-5336
Email
wanda.phipatanakul@childrens.harvard.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Gabriel Federo, MD, MPH
Phone
857-218-5336
Email
asthma@childrens.harvard.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Wanda Phipatanakul, MD, MS
Organizational Affiliation
Boston Children's Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Phoenix Children's Hospital
City
Phoenix
State/Province
Arizona
ZIP/Postal Code
85016
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Cindy Bauer, MD.
Phone
602-933-3666
Email
cbauer@phoenixchildrens.com
First Name & Middle Initial & Last Name & Degree
Songhee Han
Phone
602-933-5067
Email
shan@phoenixchildrens.com
First Name & Middle Initial & Last Name & Degree
Cindy Bauer, MD.
Facility Name
Rady Children's Hospital - San Diego
City
San Diego
State/Province
California
ZIP/Postal Code
92123
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Diba Mortazavi
Phone
858-966-1700
Ext
3422
Email
dmortazavi@ucsd.edu
First Name & Middle Initial & Last Name & Degree
Sydney Leibel, MD.
Facility Name
Childrens Hospital Colorado
City
Aurora
State/Province
Colorado
ZIP/Postal Code
80045
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Childrens H Colorado
First Name & Middle Initial & Last Name & Degree
Megan Bandeira
Phone
720-777-6860
Email
Megan.Bandeira@childrenscolorado.org
First Name & Middle Initial & Last Name & Degree
Andrew Liu, MD
Facility Name
Connecticut Children's Hospital
City
Hartford
State/Province
Connecticut
ZIP/Postal Code
06106
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Masai McIntosh, MD
Phone
860-837-7568
Email
mmcintosh@connecticutchildrens.org
First Name & Middle Initial & Last Name & Degree
Craig Lapin, MD
Facility Name
Children's National Medical Center
City
Washington
State/Province
District of Columbia
ZIP/Postal Code
20010
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Alicia Mathis
Phone
202-476-4698
Email
ANewcome@childrensnational.org
First Name & Middle Initial & Last Name & Degree
Stephen Teach, MD. MPH.
Facility Name
Emory University
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30322
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Morgan Nicholls, PhD, NP
Phone
404-785-2958
Email
morgan.nicholls@choa.org
First Name & Middle Initial & Last Name & Degree
Anne Fitzpatrick, PhD, NP.
Facility Name
Ann & Robert H. Lurie Children's Hospital of Chicago
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60611
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Melanie M. Makhija, MD. MS
Phone
312-227-6010
Email
mmakhija@luriechildrens.org
First Name & Middle Initial & Last Name & Degree
Michelle Catalano, BS,LPN,CCRP
Phone
(312) 227-6455
Email
MCatalano@luriechildrens.org
First Name & Middle Initial & Last Name & Degree
Melanie Makhija, MD.MS.
Facility Name
Indiana University/Riley Children's Hospital
City
Indianapolis
State/Province
Indiana
ZIP/Postal Code
46202
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Lori Shively, RN, CCRC
Phone
317-278-7121
Email
lashivel@iu.edu
First Name & Middle Initial & Last Name & Degree
Kirsten Kloepfer, MD
Facility Name
Boston Children's Hospital
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02115
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Gabriel Federo, MD.
Phone
857-218-5336
Email
gabriel.federohungria@childrens.harvard.edu
First Name & Middle Initial & Last Name & Degree
Wanda Phipatanakul, MD. MSc.
Facility Name
Washington University
City
Saint Louis
State/Province
Missouri
ZIP/Postal Code
63110
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Tina Norris, CRTT
Phone
314-368-0208
Email
norris.t@wustl.edu
First Name & Middle Initial & Last Name & Degree
Jeffrey Stokes, MD
Facility Name
Cincinnati Children's Hospital Medical Center
City
Cincinnati
State/Province
Ohio
ZIP/Postal Code
45229
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Emily Capal, BS
Phone
513-636-7886
Email
Emily.Capal@cchmc.org
First Name & Middle Initial & Last Name & Degree
Theresa Guilbert, MD.
Facility Name
Texas Children's Hospital/Baylor College of Medicine
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Daisy Tran
Phone
832-824-3640
Email
Dxtran1@texaschildrens.org
First Name & Middle Initial & Last Name & Degree
Carla Davis, MD
Facility Name
University of Wisconsin
City
Madison
State/Province
Wisconsin
ZIP/Postal Code
53792
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Michelle Olson
Phone
608-263-3360
Email
mrolson@medicine.wisc.edu
First Name & Middle Initial & Last Name & Degree
Daniel Jackson, MD

12. IPD Sharing Statement

Citations:
PubMed Identifier
33242697
Citation
Phipatanakul W, Mauger DT, Guilbert TW, Bacharier LB, Durrani S, Jackson DJ, Martinez FD, Fitzpatrick AM, Cunningham A, Kunselman S, Wheatley LM, Bauer C, Davis CM, Geng B, Kloepfer KM, Lapin C, Liu AH, Pongracic JA, Teach SJ, Chmiel J, Gaffin JM, Greenhawt M, Gupta MR, Lai PS, Lemanske RF, Morgan WJ, Sheehan WJ, Stokes J, Thorne PS, Oettgen HC, Israel E; PARK Study Team. Preventing asthma in high risk kids (PARK) with omalizumab: Design, rationale, methods, lessons learned and adaptation. Contemp Clin Trials. 2021 Jan;100:106228. doi: 10.1016/j.cct.2020.106228. Epub 2020 Nov 24.
Results Reference
derived
PubMed Identifier
30954166
Citation
Martinez FD. Childhood Asthma Inception and Progression: Role of Microbial Exposures, Susceptibility to Viruses and Early Allergic Sensitization. Immunol Allergy Clin North Am. 2019 May;39(2):141-150. doi: 10.1016/j.iac.2018.12.001.
Results Reference
derived

Learn more about this trial

Preventing Asthma in High Risk Kids

We'll reach out to this number within 24 hrs