Aztreonam for Inhalation Solution (AZLI) for the Treatment of Exacerbations of Cystic Fibrosis (AZTEC-CF)
Primary Purpose
Cystic Fibrosis, Infection, Pseudomonas
Status
Completed
Phase
Phase 4
Locations
United Kingdom
Study Type
Interventional
Intervention
Aztreonam
Standard Care
Sponsored by
About this trial
This is an interventional treatment trial for Cystic Fibrosis
Eligibility Criteria
Inclusion Criteria:
- Confirmed diagnosis of CF
- Patients aged 18 - 65 years of age who can give informed consent
- FEV1 >25% or <75% predicted (in keeping with Cayston® license)
- Admitted to the Liverpool Heart & Chest Hospital with an exacerbation of CF pulmonary disease
- Presence of PA in lower respiratory tract cultures in the 6 months prior
Exclusion Criteria:
- Documented allergy to beta-lactam antibiotics or IV Colistin
- Growth of Burkholderia Cepacia Complex (BCC) within 2 years
- Pregnancy
- Previous organ transplant
- Receiving other clinical trial medication
- Already prescribed regular Cayston®
Sites / Locations
- Liverpool Heart & Chest Hospital NHS Trust
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
AZLI then Standard Care
Standard Care then AZLI
Arm Description
Upon first exacerbation this arm will receive AZLI, on their second they will receive standard care
Upon first exacerbation this arm will receive standard care, on the second exacerbation this arm will receive AZLI
Outcomes
Primary Outcome Measures
Average actual change in percent predicted forced expiratory volume at 1 second (FEV1) from Day 1 to Day 14
The actual change in FEV1 (%predicted) from Day 1 of admission to Day 7 & Day 14
Secondary Outcome Measures
Time to first pulmonary exacerbation
Time from discharge to next pulmonary exacerbation
Average change from baseline in the Cystic Fibrosis Quality of Life Questionnaire (CFQ-R)
Average change from baseline (Day 1) in the CFQ-R Respiratory Symptom Score (RSS) at the end (Day 14) of each arm of the study
Microbiome changes
Changes in the structure and composition of the microbiome at the beginning and end of each treatment arm
PA sputum counts
Changes in sputum PA counts from the beginning to end of each treatment arm.
Antimicrobial resistance
Prevalence of resistance to antibiotics at the beginning and end of each treatment arm.
Full Information
NCT ID
NCT02894684
First Posted
September 1, 2016
Last Updated
October 3, 2019
Sponsor
Liverpool Heart and Chest Hospital NHS Foundation Trust
Collaborators
University of Liverpool
1. Study Identification
Unique Protocol Identification Number
NCT02894684
Brief Title
Aztreonam for Inhalation Solution (AZLI) for the Treatment of Exacerbations of Cystic Fibrosis
Acronym
AZTEC-CF
Official Title
Aztreonam for Inhalation Solution (AZLI) for the Treatment of Exacerbations of Cystic Fibrosis. An Randomised, Crossover Pilot Study of AZLI Plus Intravenous Colistin® Versus Standard Dual Intravenous Therapy
Study Type
Interventional
2. Study Status
Record Verification Date
October 2019
Overall Recruitment Status
Completed
Study Start Date
January 2017 (Actual)
Primary Completion Date
February 2019 (Actual)
Study Completion Date
September 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Liverpool Heart and Chest Hospital NHS Foundation Trust
Collaborators
University of Liverpool
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
This study evaluates the role of AZLI in the treatment of acute pulmonary exacerbations of CF. For consecutive exacerbations patients will receive AZLI + IV Colistin, or two IV anti-pseudomonals.
Detailed Description
AZLI, marketed as Cayston, is an inhaled beta-lactam antibiotic. It has a license for the chronic suppression of Pseudomonas aeruginosa (PA). Current standard practice dictates the use of two IV antipseudomonal antibiotics for the treatment of acute pulmonary exacerbations. The increasing survival, and hence population, in CF means that newer antimicrobial strategies are required in order to manage antimicrobial resistance, minimise adverse systemic effects of heavy antimicrobial exposure and also make effective use of resources. Inhaled antibiotics are commonly used in the chronic suppression of PA yet their use has not been thoroughly investigated in acute pulmonary exacerbation. Inhaled antibiotics deliver their drugs directly to the target-site with minimal systemic absorbance, making them an attractive candidate for treatment of acute exacerbations.
Recently, it has become apparent that the bacterial community is much more complex than initially thought. The microbiome, a term used to describe the polymicrobial community in the lungs, has become apparent due to the use of modern culture-independent methods to detect bacteria. The microbiome changes in composition and structure around the time of exacerbations and in response to treatment, although these changes have not been prospectively characterised.
We have designed an open-label randomised, controlled cross-over trial to investigate the clinical effectiveness of of AZLI in the treatment of acute pulmonary exacerbation, whilst simultaneously comparing the effect inhaled and intravenous antibiotics have on the microbiome.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cystic Fibrosis, Infection, Pseudomonas
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
16 (Actual)
8. Arms, Groups, and Interventions
Arm Title
AZLI then Standard Care
Arm Type
Experimental
Arm Description
Upon first exacerbation this arm will receive AZLI, on their second they will receive standard care
Arm Title
Standard Care then AZLI
Arm Type
Active Comparator
Arm Description
Upon first exacerbation this arm will receive standard care, on the second exacerbation this arm will receive AZLI
Intervention Type
Drug
Intervention Name(s)
Aztreonam
Other Intervention Name(s)
Cayston, AZLI
Intervention Description
14 days of AZLI: 75mg TDS PLUS IV Colistin
Intervention Type
Drug
Intervention Name(s)
Standard Care
Intervention Description
14 days of IV Colistin plus one of Tazocin/Ceftazidime/Meropenem/Aztreonam/Fosfomycin
Primary Outcome Measure Information:
Title
Average actual change in percent predicted forced expiratory volume at 1 second (FEV1) from Day 1 to Day 14
Description
The actual change in FEV1 (%predicted) from Day 1 of admission to Day 7 & Day 14
Time Frame
14 days
Secondary Outcome Measure Information:
Title
Time to first pulmonary exacerbation
Description
Time from discharge to next pulmonary exacerbation
Time Frame
12 months
Title
Average change from baseline in the Cystic Fibrosis Quality of Life Questionnaire (CFQ-R)
Description
Average change from baseline (Day 1) in the CFQ-R Respiratory Symptom Score (RSS) at the end (Day 14) of each arm of the study
Time Frame
14 days
Title
Microbiome changes
Description
Changes in the structure and composition of the microbiome at the beginning and end of each treatment arm
Time Frame
14 days
Title
PA sputum counts
Description
Changes in sputum PA counts from the beginning to end of each treatment arm.
Time Frame
14 days
Title
Antimicrobial resistance
Description
Prevalence of resistance to antibiotics at the beginning and end of each treatment arm.
Time Frame
14 days
10. Eligibility
Sex
Male
Minimum Age & Unit of Time
16 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Confirmed diagnosis of CF
Patients aged 18 - 65 years of age who can give informed consent
FEV1 >25% or <75% predicted (in keeping with Cayston® license)
Admitted to the Liverpool Heart & Chest Hospital with an exacerbation of CF pulmonary disease
Presence of PA in lower respiratory tract cultures in the 6 months prior
Exclusion Criteria:
Documented allergy to beta-lactam antibiotics or IV Colistin
Growth of Burkholderia Cepacia Complex (BCC) within 2 years
Pregnancy
Previous organ transplant
Receiving other clinical trial medication
Already prescribed regular Cayston®
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Freddy Frost, BMBS BMedSci
Organizational Affiliation
Liverpool Heart & Chest Hospital NHS Foundation Trust
Official's Role
Principal Investigator
Facility Information:
Facility Name
Liverpool Heart & Chest Hospital NHS Trust
City
Liverpool
ZIP/Postal Code
L3 9BZ
Country
United Kingdom
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
33358119
Citation
Frost F, Young GR, Wright L, Miah N, Smith DL, Winstanley C, Walshaw MJ, Fothergill JL, Nazareth D. The clinical and microbiological utility of inhaled aztreonam lysine for the treatment of acute pulmonary exacerbations of cystic fibrosis: An open-label randomised crossover study (AZTEC-CF). J Cyst Fibros. 2021 Nov;20(6):994-1002. doi: 10.1016/j.jcf.2020.12.012. Epub 2021 Jan 7.
Results Reference
derived
Learn more about this trial
Aztreonam for Inhalation Solution (AZLI) for the Treatment of Exacerbations of Cystic Fibrosis
We'll reach out to this number within 24 hrs