CF, Cystic Fibrosis, Lung Infection, Pseudomonas Aeruginosa
Conditions
Keywords
cystic fibrosis, CF, aztreonam, lung infection, Pseudomonas aeruginosa
Brief summary
This is multicenter placebo-controlled study evaluating the safety and efficacy of AI at two dosage levels compared to placebo in CF patients with P. aeruginosa lung infection.
Detailed description
This is multicenter placebo-controlled study evaluating the safety and efficacy of a 14-day treatment of AI at two dosage levels as compared to placebo, given twice daily, in CF patients with P. aeruginosa lung infection, delivered by the eFlow investigational nebulizer.
Interventions
DRUGAztreonam for Inhalation (AI)
Aztreonam for Inhalation
DRUGPlacebo
Saline Placebo
Sponsors
Salus Pharma, Inc.
Gilead Sciences
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
13 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Written informed consent prior to the performance of any study related procedures. * 13 years of age and above. * Documented sweat chloride ≥ 60 mEq/L by quantitative pilocarpine iontophoresis test (QPIT) or homozygosity for ΔF508 genetic mutation or heterozygosity for two well characterized mutations. * Ability to perform pulmonary function tests. * FEV1 ≥ 40% predicted at Visit 1 (Screening). * SaO2 ≥ 90% at Visit 1 (Screening). * P. aeruginosa present in sputum at Visit 1 (Screening). * Ability to expectorate sputum on a daily basis.
Exclusion criteria
* Administration of any antibiotic with antipseudomonal activity by any route within 56 days prior to Visit 1 (Screening). * Administration of any investigational drug or device within 28 days of Visit 1 (Screening) and within 6 half-lives of the investigational drug. * Oral corticosteroids in doses exceeding 10 mg per day or 20 mg every other day. * History of sputum culture or throat swab culture yielding B. cepacia in the previous two years. * Current daily continuous oxygen supplementation or requirement for more than 2 L/min at night. * Known local or systemic hypersensitivity to monobactam antibiotics. * Changes in antimicrobial, bronchodilator, anti-inflammatory or corticosteroid medications within 7 days prior to Visit 1 (Screening). * Changes in physiotherapy technique or schedule within 7 days prior to Visit 1 (Screening). * History of lung transplantation. * A chest radiograph at Visit 1 (Screening) or within the previous 90 days of Screening, with abnormalities indicating a significant acute finding (eg, lobar infiltrate and atelectasis, pneumothorax, or pleural effusion). * Abnormal renal or hepatic function or serum chemistry at Visit 1 (Screening): * AST, ALT \> 2.5 times upper limit of normal range. * Creatinine \> 1.5 times upper limit of normal range. * Positive pregnancy test. All women of childbearing potential will be tested. * Female of childbearing potential who is lactating or is not practicing acceptable method of birth control (eg, hormonal or barrier methods, or IUD). * Findings at Visit 1 (Screening) that, in the investigator's opinion, would compromise the safety of the patient or the quality of the study data.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change in FEV1 from Baseline to Day 14 | 14 Days |
Countries
United States
Outcome results
None listed