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Phase 3 N=61 Treatment

Safety of AZLI in Children With Cystic Fibrosis (CF) and Chronic Pseudomonas Aeruginosa in the Lower Airways

Cystic Fibrosis · Pseudomonas Aeruginosa

Enrolled (actual)
61
Serious AEs
21.3%
Results posted
May 2014
Primary outcome: Primary: Percentage of Participants Who Discontinued Study Drug Due to Safety or Tolerability Reasons — 0.0 percentage of participants

Study Design & Population

Study type
Interventional
Phase
Phase 3
Interventions
AZLI (Drug)
Age
Pediatric
Sex
All
Sponsor
Gilead Sciences
Primary completion
Apr 2013

Outcome Measures

OutcomeResultp-value
PRIMARY
Percentage of Participants Who Discontinued Study Drug Due to Safety or Tolerability Reasons
0.0
SECONDARY
Change From Baseline in FEV1 % Predicted in Subjects Aged ≥ 6 Years
4.73; 1.72; 1.65
SECONDARY
Change From Baseline in CFQ-R Respiratory Symptoms Scale (RSS) Score in Subjects Aged ≥ 6 Years
8.66; 9.38; 5.90
SECONDARY
Change in Pseudomonas Aeruginosa (PA) Sputum Density
-2.6; -2.0; -1.2
SECONDARY
Percentage of Participants Who Used Additional (Non-study) Antipseudomonal Antibiotics
42.6; 57.4
SECONDARY
Percentage of Participants Hospitalized at Least Once Due to a Respiratory Event
82.0; 18.0
SECONDARY
Number of Days Participants Were Hospitalized Due to a Respiratory Event
12.6
SECONDARY
Percentage of Participants With Pulmonary Exacerbations
62.3; 37.7
SECONDARY
Time to Pulmonary Exacerbation
176.0
SECONDARY
Percentage of Participants With Study-drug Induced Bronchospasm
3.3
SECONDARY
Adverse Event Rates Adjusted for Study Duration
0.163; 0.050; 0.041; 0.033; 0.033; 0.030

Summary

This was an open-label, multicenter study in children ≤ 12 years of age with cystic fibrosis (CF) and chronic Pseudomonas aeruginosa (PA) infection in the lower airways using three 28-day courses of Aztreonam for Inhalation Solution (AZLI) 75 mg three times daily, each followed by 28 days off AZLI. The total treatment duration was to be 6 months.

Eligibility Criteria

Inclusion Criteria

  • Diagnosis of CF as determined by the 1997 CF Consensus Conference criteria:
  • Documented sweat chloride ≥ 60 mEq/L by quantitative pilocarpine iontophoresis test OR
  • Abnormal nasal transepithelial potential difference (NPD) test OR
  • A genotype with 2 identifiable mutations consistent with CF AND
  • One or more clinical features consistent with CF.
  • Documented positive lower respiratory tract culture for PA at the screening visit plus two documented positive lower respiratory tract cultures for PA within 12 months prior to study entry (must have been a minimum 3 months apart.)
  • Clinically stable with no evidence of significant respiratory symptoms or, if obtained for clinical evaluation, no chest radiograph findings at screening that would have required administration of IV antipseudomonal antibiotics, oxygen supplementation, or hospitalization.

Exclusion Criteria

  • Use of IV or inhaled antipseudomonal antibiotics within 14 days of study entry
  • Presence of a condition or abnormality that would have compromised the participant's safety or the quality of study data, in the opinion of the investigator
  • History of sputum or throat swab culture yielding Burkholderia spp. within 2 years prior to screening visit
  • History of hypersensitivity/adverse reaction to aztreonam
  • History of hypersensitivity/adverse reaction to beta-agonists
  • History of lung transplantation
  • Administration of any investigational drug or device within 30 days prior to screening visit or within 6 half-lives of the investigational drug (whichever was longer)
  • Hospitalization for pulmonary-related illness within 28 days prior to screening visit
  • Changes in or initiation of chronic azithromycin treatment within 28 days prior to screening visit
  • Changes in or initiation of hypertonic saline treatment within 7 days prior to screening visit; for subjects on a stable regimen of hypertonic saline (28 days on/28 days off), beginning or ending a cycle of hypertonic saline was allowed
  • Changes in antimicrobial, bronchodilator (BD), corticosteroid or dornase alfa medications within 7 days prior to screening visit;
  • Changes in physiotherapy technique or schedule within 7 days prior to screening visit
  • Abnormal renal or hepatic function results at most recent test within the previous 90 days
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01404234). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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