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Investigating Treatment With Dupilumab in Patients With Allergic Bronchopulmonary Aspergillosis (ABPA) (LIBERTY ABPA AIRED)

Primary Purpose

Allergic Bronchopulmonary Aspergillosis

Status
Active
Phase
Phase 2
Locations
International
Study Type
Interventional
Intervention
dupilumab
Placebo
Sponsored by
Regeneron Pharmaceuticals
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Allergic Bronchopulmonary Aspergillosis

Eligibility Criteria

12 Years - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Key Inclusion Criteria:

  • Diagnosis of both ABPA and asthma
  • On a maintenance therapy for their asthma with controller medication which must include inhaled corticosteroids (ICS) and may include 1 or more additional controller medications including a long-acting beta agonist (LABA), leukotriene receptor antagonist (LTRA), and/or long-acting muscarinic receptor antagonist (LAMA), etc for at least 12 weeks, with a stable dose and regimen with no change in the dose or frequency of administration for at least 4 weeks prior to the screening visit and between the screening and baseline/randomization visits
  • For participants on OCS (oral corticosteroid): must be on a chronic stable dose (no change in the dose) of OCS of up to 10 mg/day (for participants taking daily corticosteroids) or 30 mg every alternate day (for participants taking alternate day corticosteroids) (prednisone/prednisolone or the equivalent) for at least 4 weeks prior to the screening visit and between the screening and the baseline/randomization visit
  • Must have experienced ≥1 severe respiratory exacerbation requiring treatment with systemic corticosteroids or hospitalization or treatment in ED/urgent care within 12 months prior to the screening visit or must be receiving chronic stable low-dose OCS per above criteria

Key Exclusion Criteria:

  • Weight less than 30.0 kilograms
  • Current smoker or e-cigarette user, cessation of smoking or e-cigarette use within 6 months prior to randomization, or >10 pack-years smoking history
  • Post-bronchodilator FEV1 <30% predicted normal at screening
  • Respiratory exacerbation requiring systemic corticosteroids within 4 weeks prior to screening and between screening and baseline visit (for patients on daily OCS, exacerbation requiring at least doubling of the daily maintenance dose of corticosteroids)
  • Upper or lower respiratory tract infection within the 4 weeks prior to screening (visit 1) or between the screening and randomization visits
  • Significant chronic pulmonary disease other than asthma complicated with ABPA (eg, physician-diagnosed bronchiectasis due to a condition other than ABPA; cystic fibrosis; sarcoidosis; interstitial lung disease not due to ABPA; chronic obstructive pulmonary disease [COPD] not due to ABPA; hypereosinophilic syndrome; etc), a diagnosed pulmonary or systemic disease associated with elevated peripheral eosinophil counts
  • Diagnosis or suspected diagnosis of eosinophilic granulomatosis with polyangiitis (EGPA) (also called Churg-Strauss Syndrome)

NOTE: Other protocol defined inclusion / exclusion criteria applies.

Sites / Locations

  • Regeneron Study Site
  • Regeneron Study Site
  • Regeneron Study Site
  • Regeneron Study Site
  • Regeneron Study Site
  • Regeneron Study Site
  • Regeneron Study Site
  • Regeneron Study Site
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  • Regeneron Study Site
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  • Regeneron Study Site
  • Regeneron Study Site
  • Regeneron Study Site
  • Regeneron Study Site
  • Regeneron Study Site
  • Regeneron Study Site
  • Regeneron Study Site
  • Regeneron Study Site
  • Regeneron Study Site
  • Regeneron Study Site
  • Regeneron Study Site
  • Regeneron Study Site
  • Regeneron Study Site
  • Regeneron Study Site
  • Regeneron Study Site
  • Regeneron Study Site
  • Regeneron Study Site
  • Regeneron Study Site
  • Regeneron Study Site
  • Regeneron Study Site
  • Regeneron Study Site
  • Regeneron Study Site
  • Regeneron Study Site
  • Regeneron Study Site
  • Regeneron Study Site
  • Regeneron Study Site
  • Regeneron Study Site
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  • Regeneron Study Site
  • Regeneron Study Site
  • Regeneron Study Site
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  • Regeneron Study Site
  • Regeneron Study Site
  • Regeneron Study Site
  • Regeneron Study Site
  • Regeneron Study Site
  • Regeneron Study Site
  • Regeneron Study Site
  • Regeneron Study Site
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  • Regeneron Study Site
  • Regeneron Study Site
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  • Regeneron Study Site
  • Regeneron Study Site
  • Regeneron Study Site
  • Regeneron Study Site
  • Regeneron Study Site
  • Regeneron Study Site
  • Regeneron Study Site
  • Regeneron Study Site
  • Regeneron Study Site
  • Regeneron Study Site
  • Regeneron Study Site

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

dupilumab

Placebo

Arm Description

Loading subcutaneous (SC) dose on day 1, followed by SC dose, every two weeks (Q2W)

Matching dupilumab without active substance

Outcomes

Primary Outcome Measures

Change from baseline in pre-bronchodilator forced expiratory volume in 1 second (FEV1) compared to placebo

Secondary Outcome Measures

Annualized rate of severe respiratory exacerbations
Defined as new onset of symptoms or clinical worsening of respiratory symptoms requiring systemic corticosteroid treatment for ≥3 consecutive days; for patients who are on maintenance systemic corticosteroids, at least double the dose of maintenance systemic corticosteroids for ≥3 consecutive days (with or without antibiotic therapy if indicated)
Annualized rate of ABPA-related exacerbations
Defined as severe respiratory exacerbations (as defined above) that are associated with a doubling of serum total Immunoglobulin E (IgE) from the prior pre-exacerbation value.
Annualized rate of severe respiratory exacerbations requiring either hospitalization or observation for >24 hours in an ED/urgent care facility
Change from baseline in Asthma Control Questionnaire (ACQ)-5
ACQ is completed by patient to measure both the adequacy of asthma control and change in asthma control, which occurs either spontaneously or as a result of treatment. The ACQ-5 score is the mean of the first 5 questions, between 0 (totally controlled) and 6 (severely uncontrolled). A higher score indicates lower asthma control. Patients with a score below 1.0 reflect adequately controlled asthma and patients with scores above 1.0 reflect inadequately controlled asthma. The optimal cut-point score of 1.50 should be used to be confident that a patient has inadequately controlled asthma.
Change from baseline in St. George's Respiratory Questionnaire (SGRQ) total score
SGRQ will be completed by the patient to measure and quantify health status in adult patients with chronic airflow limitation. Total score ranges from 0 to 100. Scores by dimension are calculated for three domains: Symptoms, Activity, and Impacts (Psychosocial). Lower score indicates better Quality of Life (QoL).
Percentage of participants achieving a reduction in the SGRQ score of 4 points or greater from baseline
SGRQ will be completed by the patient to measure and quantify health status in adult patients with chronic airflow limitation. Total score ranges from 0 to 100. Scores by dimension are calculated for three domains: Symptoms, Activity, and Impacts (Psychosocial). Lower score indicates better Quality of Life (QoL).
Percent change from baseline in total IgE in serum
Percent change from baseline in A fumigatus-specific IgE in serum
Percent change from baseline in fractional exhaled nitric oxide (FeNO)
Absolute change from baseline in FeNO
Incidence of treatment-emergent adverse events (TEAEs) from baseline
Incidence of treatment-emergent anti-drug antibody (ADA) responses and titer over time
Concentrations of functional dupilumab in serum by treatment regimen

Full Information

First Posted
June 4, 2020
Last Updated
April 3, 2023
Sponsor
Regeneron Pharmaceuticals
Collaborators
Sanofi
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1. Study Identification

Unique Protocol Identification Number
NCT04442269
Brief Title
Investigating Treatment With Dupilumab in Patients With Allergic Bronchopulmonary Aspergillosis (ABPA) (LIBERTY ABPA AIRED)
Official Title
A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study to Evaluate the Efficacy and Safety of Dupilumab in Patients With Allergic Bronchopulmonary Aspergillosis
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
September 15, 2020 (Actual)
Primary Completion Date
August 21, 2023 (Anticipated)
Study Completion Date
November 13, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Regeneron Pharmaceuticals
Collaborators
Sanofi

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
The primary objective of the study is to evaluate the efficacy of dupilumab on lung function in participants with Allergic Bronchopulmonary Aspergillosis (ABPA). The secondary objectives of the study are: To evaluate the effects of dupilumab on exacerbations in participants with ABPA To evaluate the effects of dupilumab on ABPA-related exacerbations To evaluate the effects of dupilumab on hospitalization/emergency department (ED)/urgent care visits in participants with ABPA To evaluate the effects of dupilumab on asthma control in participants with ABPA To evaluate the effects of dupilumab on health-related quality of life (HRQoL) in participants with ABPA To evaluate the effects of dupilumab on serum total immunoglobulin E (IgE) and Aspergillus-specific IgE concentrations To evaluate the effects of dupilumab on Fractional exhaled Nitric Oxide (FeNO) levels To evaluate safety and tolerability of dupilumab in participants with ABPA To evaluate dupilumab concentrations in serum and the incidence of anti-dupilumab antibodies in participants with ABPA

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Allergic Bronchopulmonary Aspergillosis

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
62 (Actual)

8. Arms, Groups, and Interventions

Arm Title
dupilumab
Arm Type
Experimental
Arm Description
Loading subcutaneous (SC) dose on day 1, followed by SC dose, every two weeks (Q2W)
Arm Title
Placebo
Arm Type
Experimental
Arm Description
Matching dupilumab without active substance
Intervention Type
Drug
Intervention Name(s)
dupilumab
Other Intervention Name(s)
• DUPIXENT, • REGN668, • SAR231893
Intervention Description
Single-use prefilled glass syringe administered by subcutaneous (SC) injection.
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Matching placebo
Primary Outcome Measure Information:
Title
Change from baseline in pre-bronchodilator forced expiratory volume in 1 second (FEV1) compared to placebo
Time Frame
At Week 24
Secondary Outcome Measure Information:
Title
Annualized rate of severe respiratory exacerbations
Description
Defined as new onset of symptoms or clinical worsening of respiratory symptoms requiring systemic corticosteroid treatment for ≥3 consecutive days; for patients who are on maintenance systemic corticosteroids, at least double the dose of maintenance systemic corticosteroids for ≥3 consecutive days (with or without antibiotic therapy if indicated)
Time Frame
Over the 24 to 52 Week Treatment Period
Title
Annualized rate of ABPA-related exacerbations
Description
Defined as severe respiratory exacerbations (as defined above) that are associated with a doubling of serum total Immunoglobulin E (IgE) from the prior pre-exacerbation value.
Time Frame
Over the 24 to 52 Week Treatment Period
Title
Annualized rate of severe respiratory exacerbations requiring either hospitalization or observation for >24 hours in an ED/urgent care facility
Time Frame
Over the 24 to 52 Week Treatment Period
Title
Change from baseline in Asthma Control Questionnaire (ACQ)-5
Description
ACQ is completed by patient to measure both the adequacy of asthma control and change in asthma control, which occurs either spontaneously or as a result of treatment. The ACQ-5 score is the mean of the first 5 questions, between 0 (totally controlled) and 6 (severely uncontrolled). A higher score indicates lower asthma control. Patients with a score below 1.0 reflect adequately controlled asthma and patients with scores above 1.0 reflect inadequately controlled asthma. The optimal cut-point score of 1.50 should be used to be confident that a patient has inadequately controlled asthma.
Time Frame
Over the 24 to 52 Week Treatment Period
Title
Change from baseline in St. George's Respiratory Questionnaire (SGRQ) total score
Description
SGRQ will be completed by the patient to measure and quantify health status in adult patients with chronic airflow limitation. Total score ranges from 0 to 100. Scores by dimension are calculated for three domains: Symptoms, Activity, and Impacts (Psychosocial). Lower score indicates better Quality of Life (QoL).
Time Frame
Over the 24 to 52 Week Treatment Period
Title
Percentage of participants achieving a reduction in the SGRQ score of 4 points or greater from baseline
Description
SGRQ will be completed by the patient to measure and quantify health status in adult patients with chronic airflow limitation. Total score ranges from 0 to 100. Scores by dimension are calculated for three domains: Symptoms, Activity, and Impacts (Psychosocial). Lower score indicates better Quality of Life (QoL).
Time Frame
Up to 52 Weeks
Title
Percent change from baseline in total IgE in serum
Time Frame
Over the 24 to 52 Week Treatment Period
Title
Percent change from baseline in A fumigatus-specific IgE in serum
Time Frame
Over the 24 to 52 Week Treatment Period
Title
Percent change from baseline in fractional exhaled nitric oxide (FeNO)
Time Frame
Over the 24 to 52 Week Treatment Period
Title
Absolute change from baseline in FeNO
Time Frame
Over the 24 to 52 Week Treatment Period
Title
Incidence of treatment-emergent adverse events (TEAEs) from baseline
Time Frame
Through the end of the 52 Week Treatment Period
Title
Incidence of treatment-emergent anti-drug antibody (ADA) responses and titer over time
Time Frame
Up to 64 Weeks
Title
Concentrations of functional dupilumab in serum by treatment regimen
Time Frame
Up to 64 Weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
12 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Key Inclusion Criteria: Diagnosis of both ABPA and asthma On a maintenance therapy for their asthma with controller medication which must include inhaled corticosteroids (ICS) and may include 1 or more additional controller medications including a long-acting beta agonist (LABA), leukotriene receptor antagonist (LTRA), and/or long-acting muscarinic receptor antagonist (LAMA), etc for at least 12 weeks, with a stable dose and regimen with no change in the dose or frequency of administration for at least 4 weeks prior to the screening visit and between the screening and baseline/randomization visits For participants on OCS (oral corticosteroid): must be on a chronic stable dose (no change in the dose) of OCS of up to 10 mg/day (for participants taking daily corticosteroids) or up to 30 mg every alternate day (for participants taking alternate day corticosteroids) (prednisone/prednisolone or the equivalent) for at least 4 weeks prior to the screening visit and between the screening and the baseline/randomization visit Must have experienced ≥1 severe respiratory exacerbation requiring treatment with systemic corticosteroids or hospitalization or treatment in ED/urgent care within 12 months prior to the screening visit or must be receiving chronic stable low-dose OCS per above criteria Key Exclusion Criteria: Weight less than 30.0 kilograms Current smoker or e-cigarette user, cessation of smoking or e-cigarette use within 6 months prior to randomization, or >=10 pack-years smoking history Post-bronchodilator FEV1 <30% predicted normal at screening Respiratory exacerbation requiring systemic corticosteroids within 4 weeks prior to screening and between screening and baseline visit (for patients on daily or alternate day OCS, exacerbation requiring at least double the maintenance dose of corticosteroids) Upper or lower respiratory tract infection within the 4 weeks prior to screening (visit 1) or between the screening and randomization visits Significant chronic pulmonary disease other than asthma complicated with ABPA (eg, physician-diagnosed bronchiectasis due to a condition other than ABPA; cystic fibrosis; sarcoidosis; interstitial lung disease not due to ABPA; chronic obstructive pulmonary disease [COPD] not due to ABPA; hypereosinophilic syndrome; etc), a diagnosed pulmonary or systemic disease associated with elevated peripheral eosinophil counts Diagnosis or suspected diagnosis of eosinophilic granulomatosis with polyangiitis (EGPA) (also called Churg-Strauss Syndrome) NOTE: Other protocol defined inclusion / exclusion criteria applies.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Clinical Trial Management
Organizational Affiliation
Regeneron Pharmaceuticals
Official's Role
Study Director
Facility Information:
Facility Name
Regeneron Study Site
City
Birmingham
State/Province
Alabama
ZIP/Postal Code
35209
Country
United States
Facility Name
Regeneron Study Site
City
Birmingham
State/Province
Alabama
ZIP/Postal Code
35233
Country
United States
Facility Name
Regeneron Study Site
City
Scottsdale
State/Province
Arizona
ZIP/Postal Code
85251
Country
United States
Facility Name
Regeneron Study Site
City
Atherton
State/Province
California
ZIP/Postal Code
94027
Country
United States
Facility Name
Regeneron Study Site
City
Bakersfield
State/Province
California
ZIP/Postal Code
93301
Country
United States
Facility Name
Regeneron Study Site
City
La Jolla
State/Province
California
ZIP/Postal Code
92093
Country
United States
Facility Name
Regeneron Study Site
City
Los Angeles
State/Province
California
ZIP/Postal Code
90025
Country
United States
Facility Name
Regeneron Study Site
City
Riverside
State/Province
California
ZIP/Postal Code
92506
Country
United States
Facility Name
Regeneron Study Site
City
Stockton
State/Province
California
ZIP/Postal Code
95207
Country
United States
Facility Name
Regeneron Study Site
City
Boise
State/Province
Idaho
ZIP/Postal Code
83706
Country
United States
Facility Name
Regeneron Study Site
City
Iowa City
State/Province
Iowa
ZIP/Postal Code
52242
Country
United States
Facility Name
Regeneron Study Site
City
Fort Mitchell
State/Province
Kentucky
ZIP/Postal Code
41017
Country
United States
Facility Name
Regeneron Study Site
City
Saint Louis
State/Province
Missouri
ZIP/Postal Code
63110
Country
United States
Facility Name
Regeneron Study Site
City
Brick
State/Province
New Jersey
ZIP/Postal Code
08724
Country
United States
Facility Name
Regeneron Study Site
City
Bronx
State/Province
New York
ZIP/Postal Code
10461
Country
United States
Facility Name
Regeneron Study Site
City
New York
State/Province
New York
ZIP/Postal Code
10032
Country
United States
Facility Name
Regeneron Study Site
City
Columbus
State/Province
Ohio
ZIP/Postal Code
43235
Country
United States
Facility Name
Regeneron Study Site
City
DuBois
State/Province
Pennsylvania
ZIP/Postal Code
15801
Country
United States
Facility Name
Regeneron Study Site
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19140
Country
United States
Facility Name
Regeneron Study Site
City
Haskovo
ZIP/Postal Code
6305
Country
Bulgaria
Facility Name
Regeneron Study Site
City
Razgrad
ZIP/Postal Code
7200
Country
Bulgaria
Facility Name
Regeneron Study Site
City
Smolyan
ZIP/Postal Code
4700
Country
Bulgaria
Facility Name
Regeneron Study Site
City
Sofia
ZIP/Postal Code
1142
Country
Bulgaria
Facility Name
Regeneron Study Site
City
Vancouver
State/Province
British Columbia
ZIP/Postal Code
V5Z1M9
Country
Canada
Facility Name
Regeneron Study Site
City
Ottawa
State/Province
Ontario
ZIP/Postal Code
K1G 6C6
Country
Canada
Facility Name
Regeneron Study Site
City
Montreal
State/Province
Quebec
ZIP/Postal Code
H4A3J1
Country
Canada
Facility Name
Regeneron Study Site
City
Quebec City
State/Province
Quebec
ZIP/Postal Code
G1V 4G5
Country
Canada
Facility Name
Regeneron Study Site
City
Brest
ZIP/Postal Code
29609
Country
France
Facility Name
Regeneron Study Site
City
Grenoble
ZIP/Postal Code
38043
Country
France
Facility Name
Regeneron Study Site
City
Le Mans
ZIP/Postal Code
72000
Country
France
Facility Name
Regeneron Study Site
City
Lyon
ZIP/Postal Code
69004
Country
France
Facility Name
Regeneron Study Site
City
Marseille
ZIP/Postal Code
13015
Country
France
Facility Name
Regeneron Study Site
City
Montpellier
ZIP/Postal Code
34295
Country
France
Facility Name
Regeneron Study Site
City
Paris
ZIP/Postal Code
75018
Country
France
Facility Name
Regeneron Study Site
City
Pessac
ZIP/Postal Code
33604
Country
France
Facility Name
Regeneron Study Site
City
Reims Cedex
ZIP/Postal Code
51092
Country
France
Facility Name
Regeneron Study Site
City
Rennes
ZIP/Postal Code
35033
Country
France
Facility Name
Regeneron Study Site
City
Suresnes
ZIP/Postal Code
92151
Country
France
Facility Name
Regeneron Study Site
City
Tours
ZIP/Postal Code
37044
Country
France
Facility Name
Regeneron Study Site
City
Leipzig
State/Province
Saxony
ZIP/Postal Code
4357
Country
Germany
Facility Name
Regeneron Study Site
City
Berlin
ZIP/Postal Code
10717
Country
Germany
Facility Name
Regeneron Study Site
City
Berlin
ZIP/Postal Code
13125
Country
Germany
Facility Name
Regeneron Study Site
City
Frankfurt am Main
ZIP/Postal Code
60389
Country
Germany
Facility Name
Regeneron Study Site
City
Budapest
ZIP/Postal Code
1083
Country
Hungary
Facility Name
Regeneron Study Site
City
Fukuyama
ZIP/Postal Code
7200001
Country
Japan
Facility Name
Regeneron Study Site
City
Kanagawa
ZIP/Postal Code
259-1193
Country
Japan
Facility Name
Regeneron Study Site
City
Nagoya
ZIP/Postal Code
454-8509
Country
Japan
Facility Name
Regeneron Study Site
City
Naka-gun
ZIP/Postal Code
3191113
Country
Japan
Facility Name
Regeneron Study Site
City
Sakai
ZIP/Postal Code
591-8555
Country
Japan
Facility Name
Regeneron Study Site
City
Yanagawa
ZIP/Postal Code
8320059
Country
Japan
Facility Name
Regeneron Study Site
City
Yokohama
ZIP/Postal Code
231-8682
Country
Japan
Facility Name
Regeneron Study Site
City
Amsterdam
State/Province
North Holland
ZIP/Postal Code
1105AZ
Country
Netherlands
Facility Name
Regeneron Study Site
City
Arnhem
ZIP/Postal Code
6815
Country
Netherlands
Facility Name
Regeneron Study Site
City
Breda
ZIP/Postal Code
4818 CK
Country
Netherlands
Facility Name
Regeneron Study Site
City
Eindhoven
ZIP/Postal Code
5623
Country
Netherlands
Facility Name
Regeneron Study Site
City
Zutphen
ZIP/Postal Code
7207
Country
Netherlands
Facility Name
Regeneron Study Site
City
Bialystok
ZIP/Postal Code
15-044
Country
Poland
Facility Name
Regeneron Study Site
City
Gdansk
ZIP/Postal Code
80402
Country
Poland
Facility Name
Regeneron Study Site
City
Oradea
State/Province
Bihor
ZIP/Postal Code
410169
Country
Romania
Facility Name
Regeneron Study Site
City
Brasov
ZIP/Postal Code
500051
Country
Romania
Facility Name
Regeneron Study Site
City
Bucharest
ZIP/Postal Code
011461
Country
Romania
Facility Name
Regeneron Study Site
City
Bucharest
ZIP/Postal Code
050159
Country
Romania
Facility Name
Regeneron Study Site
City
Leicester
State/Province
England
ZIP/Postal Code
LE39QP
Country
United Kingdom
Facility Name
Regeneron Study Site
City
Liverpool
State/Province
England
ZIP/Postal Code
L7 8XP
Country
United Kingdom
Facility Name
Regeneron Study Site
City
London
State/Province
England
ZIP/Postal Code
E1 2EF
Country
United Kingdom
Facility Name
Regeneron Study Site
City
London
State/Province
England
ZIP/Postal Code
SW3 6NP
Country
United Kingdom
Facility Name
Regeneron Study Site
City
Wythenshawe
State/Province
England
ZIP/Postal Code
M23 9LT
Country
United Kingdom
Facility Name
Regeneron Study Site
City
Oxford
State/Province
Oxfordshire
ZIP/Postal Code
OX3 9DU
Country
United Kingdom
Facility Name
Regeneron Study Site
City
Bradford
State/Province
West Yorkshire
ZIP/Postal Code
BD96RJ
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
All Individual Patient Data (IPD) that underlie publicly available results will be considered for sharing
IPD Sharing Time Frame
Individual anonymized participant data will be considered for sharing once the indication has been approved by a regulatory body, if there is legal authority to share the data and there is not a reasonable likelihood of participant re-identification.
IPD Sharing Access Criteria
Qualified researchers may request access to anonymized patient level data or aggregate study data when Regeneron has received marketing authorization from major health authorities (e.g., FDA, European Medicines Agency (EMA), Pharmaceuticals and Medical Devices Agency (PMDA), etc) for the product and indication, has the legal authority to share the data, and has made the study results publicly available (eg, scientific publication, scientific conference, clinical trial registry).
IPD Sharing URL
https://vivli.org/
Citations:
PubMed Identifier
33027187
Citation
Kao CC, Hanania NA, Parulekar AD. The impact of fungal allergic sensitization on asthma. Curr Opin Pulm Med. 2021 Jan;27(1):3-8. doi: 10.1097/MCP.0000000000000740.
Results Reference
derived

Learn more about this trial

Investigating Treatment With Dupilumab in Patients With Allergic Bronchopulmonary Aspergillosis (ABPA) (LIBERTY ABPA AIRED)

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