Evaluation of the Response to Monoclonal Antibody Therapy in Severe Asthma: Research of Predictive Biomarkers in Exhaled Air (Zina-VOC)
Primary Purpose
Asthma
Status
Unknown status
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
VOC analysis
Sponsored by
About this trial
This is an interventional other trial for Asthma
Eligibility Criteria
Inclusion Criteria:
- patient aged > 18 years old
- patient with severe asthma who respond to the indication of monoclonal antibody therapy according to SPC and management criteria fixed by Transparency Committee
- signed informed consent
- patient with healthcare insurance
Exclusion Criteria:
- patient not responding to the criteria for the good use of monoclonal antibody in severe asthma
- contraindication to one of monoclonal antibody treatment according to SPC (hypersensitivity to one of compounds)
- patient unable to perform a slow vital capacity
- patient with long-term oxygen therapy , under invasive ventilation
- pregnant women
- patient deprived of liberty by judicial or administrative decision
Sites / Locations
- Hôpital FochRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
VOC analysis
Arm Description
VOC analysis in exhaled air in patients with severe asthma treated by monoclonal antibody
Outcomes
Primary Outcome Measures
Change of Volatil Organic Compound (VOC) profiles predictive of clinically significant response
Clinically significant response defined by:
reduction of 50% of number of exacerbations treated by oral corticosteroids after 12 months of treatment compared to the number of exacerbation during the previous year AND/OR
increase of 3 points (MCID according to Schartz and al 2009) of ACT score after 3 months of treatment and maintained at 6 months
Secondary Outcome Measures
Change of FEV and FEV/CV
Predictive variations of a clinically relevant response with improvement of FEV and FEV/CV at 3, 6 and 12 months
Decrease of residual volume
Predictive variations of a clinically relevant response with decrease of residual volume (RV) at 3, 6 and 12 months
Decrease of the daily dose of oral corticosteroids
Predictive variations of a clinically relevant response with decrease of the daily dose of oral corticosteroids for corticosteroid-dependent patients at 1, 3, 6 and 12 months
Reduction in the number of exacerbations
50% reduction in the number of exacerbations treated with oral steroids after 6 months of treatment compared to the number of exacerbations in the previous year OR a 3 point increase in the ACT (Asthma Control Test) score after 3 months of treatment maintained at 6 months OR increase of GETE (global evaluation of treatment effectiveness) score at 1, 3, 6 and 12 months
Change before and after treatment
Change of Volatil Organic Compound (VOC) profiles before and after treatment whatever is the clinical answer
Change according to administered antibody
Change of Volatil Organic Compound (VOC) profiles according to administered antibody
Volatil Organic Compound (VOC) profiles according to patients' phenotype
Volatil Organic Compound (VOC) profiles according to patients' phenotype at the inclusion
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT03988790
Brief Title
Evaluation of the Response to Monoclonal Antibody Therapy in Severe Asthma: Research of Predictive Biomarkers in Exhaled Air
Acronym
Zina-VOC
Official Title
Evaluation of Response to Monoclonal Antibody Therapy in Severe Asthma: Research of Predictive Biomarkers in Exhaled Air
Study Type
Interventional
2. Study Status
Record Verification Date
February 2021
Overall Recruitment Status
Unknown status
Study Start Date
December 4, 2018 (Actual)
Primary Completion Date
December 31, 2022 (Anticipated)
Study Completion Date
December 31, 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hopital Foch
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
This study evaluates the change in the composition of Volatil Organic Compounds (VOC) in patients treated by monoclonal antibody for severe asthma.
Detailed Description
At least one in two patients treated by monoclonal antibody for severe asthma doesn't have satisfying result after 6 months of treatment.
The evaluation of the answer, and even better the answer prediction, are fundamental issues for medico-economic plan as part of these innovative therapeutics.
The interest of the use of VOC as diagnostic or prognostic tool in patients with tumoral thoracic pathology or bronchial or pulmonary vascular diseases has been demonstrated.
VOC analysis will be performed using two different techniques: electronic nose and masse spectrometry. At each visit, in addition to the usual assessment, patients will have two non-invasives collections of exhaled air, one for electronic nose analysis and one for masse spectrometry analysis.
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
Other
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Single Group Assignement
Masking
None (Open Label)
Allocation
N/A
Enrollment
50 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
VOC analysis
Arm Type
Experimental
Arm Description
VOC analysis in exhaled air in patients with severe asthma treated by monoclonal antibody
Intervention Type
Device
Intervention Name(s)
VOC analysis
Intervention Description
VOC analysis in exhaled air with e-noses and mass spectrometry.
Primary Outcome Measure Information:
Title
Change of Volatil Organic Compound (VOC) profiles predictive of clinically significant response
Description
Clinically significant response defined by:
reduction of 50% of number of exacerbations treated by oral corticosteroids after 12 months of treatment compared to the number of exacerbation during the previous year AND/OR
increase of 3 points (MCID according to Schartz and al 2009) of ACT score after 3 months of treatment and maintained at 6 months
Time Frame
1 day
Secondary Outcome Measure Information:
Title
Change of FEV and FEV/CV
Description
Predictive variations of a clinically relevant response with improvement of FEV and FEV/CV at 3, 6 and 12 months
Time Frame
change from baseline profiles at 3, 6 and12 months post-baseline
Title
Decrease of residual volume
Description
Predictive variations of a clinically relevant response with decrease of residual volume (RV) at 3, 6 and 12 months
Time Frame
change from baseline profiles at 3, 6 and12 months post-baseline
Title
Decrease of the daily dose of oral corticosteroids
Description
Predictive variations of a clinically relevant response with decrease of the daily dose of oral corticosteroids for corticosteroid-dependent patients at 1, 3, 6 and 12 months
Time Frame
change from baseline profiles at 1, 3, 6 and12 months post-baseline
Title
Reduction in the number of exacerbations
Description
50% reduction in the number of exacerbations treated with oral steroids after 6 months of treatment compared to the number of exacerbations in the previous year OR a 3 point increase in the ACT (Asthma Control Test) score after 3 months of treatment maintained at 6 months OR increase of GETE (global evaluation of treatment effectiveness) score at 1, 3, 6 and 12 months
Time Frame
change from baseline profiles at 1, 3, 6 and12 months post-baseline
Title
Change before and after treatment
Description
Change of Volatil Organic Compound (VOC) profiles before and after treatment whatever is the clinical answer
Time Frame
change from baseline profiles at 12 months post-baseline
Title
Change according to administered antibody
Description
Change of Volatil Organic Compound (VOC) profiles according to administered antibody
Time Frame
1 day
Title
Volatil Organic Compound (VOC) profiles according to patients' phenotype
Description
Volatil Organic Compound (VOC) profiles according to patients' phenotype at the inclusion
Time Frame
1 day
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
patient aged > 18 years old
patient with severe asthma who respond to the indication of monoclonal antibody therapy according to SPC and management criteria fixed by Transparency Committee
signed informed consent
patient with healthcare insurance
Exclusion Criteria:
patient not responding to the criteria for the good use of monoclonal antibody in severe asthma
contraindication to one of monoclonal antibody treatment according to SPC (hypersensitivity to one of compounds)
patient unable to perform a slow vital capacity
patient with long-term oxygen therapy , under invasive ventilation
pregnant women
patient deprived of liberty by judicial or administrative decision
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Elisabeth Hulier-Ammar
Phone
+33 1 46 25 11 75
Email
drci-promotion@hopital-foch.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Philippe Devillier
Organizational Affiliation
Pneumology department
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hôpital Foch
City
Suresnes
ZIP/Postal Code
92150
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Philippe Devillier
Phone
+ 33 1 46 25 27 91
Email
p.devillier@hopital-foch.com
12. IPD Sharing Statement
Learn more about this trial
Evaluation of the Response to Monoclonal Antibody Therapy in Severe Asthma: Research of Predictive Biomarkers in Exhaled Air
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