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

L

Liverpool Heart and Chest Hospital NHS Foundation Trust

Status and phase

Completed
Phase 4

Conditions

Infection
Pseudomonas
Cystic Fibrosis

Treatments

Drug: Standard Care
Drug: Aztreonam

Study type

Interventional

Funder types

Other

Identifiers

NCT02894684
2016AZLIND001

Details and patient eligibility

About

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.

Full 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.

Enrollment

16 patients

Sex

Male

Ages

16 to 65 years old

Volunteers

No Healthy Volunteers

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®

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

16 participants in 2 patient groups

AZLI then Standard Care
Experimental group
Description:
Upon first exacerbation this arm will receive AZLI, on their second they will receive standard care
Treatment:
Drug: Aztreonam
Drug: Standard Care
Standard Care then AZLI
Active Comparator group
Description:
Upon first exacerbation this arm will receive standard care, on the second exacerbation this arm will receive AZLI
Treatment:
Drug: Aztreonam
Drug: Standard Care

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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