Phase 3
N=61
Safety of AZLI in Children With Cystic Fibrosis (CF) and Chronic Pseudomonas Aeruginosa in the Lower Airways
Cystic Fibrosis · Pseudomonas Aeruginosa
Bottom Line
View on ClinicalTrials.gov: NCT01404234 ↗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
| Outcome | Result | p-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
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.