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Aztreonam for Inhalation Solution (AZLI) for the Treatment of Exacerbations of Cystic Fibrosis

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

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02894684
Acronym
AZTEC-CF
Enrollment
16
Registered
2016-09-09
Start date
2017-01-31
Completion date
2019-09-30
Last updated
2019-10-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cystic Fibrosis, Infection, Pseudomonas

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.

Interventions

14 days of AZLI: 75mg TDS PLUS IV Colistin

DRUGStandard Care

14 days of IV Colistin plus one of Tazocin/Ceftazidime/Meropenem/Aztreonam/Fosfomycin

Sponsors

University of Liverpool
CollaboratorOTHER
Liverpool Heart and Chest Hospital NHS Foundation Trust
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
16 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

1. Confirmed diagnosis of CF 2. Patients aged 18 - 65 years of age who can give informed consent 3. FEV1 \>25% or \<75% predicted (in keeping with Cayston® license) 4. Admitted to the Liverpool Heart & Chest Hospital with an exacerbation of CF pulmonary disease 5. Presence of PA in lower respiratory tract cultures in the 6 months prior

Exclusion criteria

1. Documented allergy to beta-lactam antibiotics or IV Colistin 2. Growth of Burkholderia Cepacia Complex (BCC) within 2 years 3. Pregnancy 4. Previous organ transplant 5. Receiving other clinical trial medication 6. Already prescribed regular Cayston®

Design outcomes

Primary

MeasureTime frameDescription
Average actual change in percent predicted forced expiratory volume at 1 second (FEV1) from Day 1 to Day 1414 daysThe actual change in FEV1 (%predicted) from Day 1 of admission to Day 7 & Day 14

Secondary

MeasureTime frameDescription
Time to first pulmonary exacerbation12 monthsTime from discharge to next pulmonary exacerbation
Average change from baseline in the Cystic Fibrosis Quality of Life Questionnaire (CFQ-R)14 daysAverage 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 changes14 daysChanges in the structure and composition of the microbiome at the beginning and end of each treatment arm
PA sputum counts14 daysChanges in sputum PA counts from the beginning to end of each treatment arm.
Antimicrobial resistance14 daysPrevalence of resistance to antibiotics at the beginning and end of each treatment arm.

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 20, 2026