Prospective, randomized, placebo controlled, phase II clinical study of subjects crossing over from an approved inhaled antibiotic to inhaled nitric oxide as compared to a placebo control arm.
This is a multi-center, randomized, placebo controlled, phase II clinical study comparing an investigational drug to a placebo control. Screening data will be reviewed to determine subject eligibility. All subjects including screen failure subjects will be recorded on screening logs at their respective sites. Upon successful completion of all screening procedures, a subject will be considered eligible for enrollment. The subject will be enrolled and randomized in as close a time proximity to the first treatment application as is possible in order to minimize the possibility of dropout while enrolled but before undergoing treatment. With a 1:1 investigational treatment to placebo control, subjects will be randomized to one of the two arms. Subjects in the investigational treatment arm will be administered doses of NO (0.5% NO in 99.5% nitrogen) diluted in room air by inhalation four times daily (30-minute inhalations at least 3 hours apart) for 7.5 days on Days 1, 2, 3, 4, 5, 8, 9, and 10 (three treatments on Days 1 and 10). Subjects in the placebo arm will breathe 100% nitrogen diluted in room air in the same proportion as the investigational arm. Subjects will remain in the clinic for 30 minutes after completing the last treatment of each day. All subjects will be asked to return to the clinic for additional evaluations on Days 15 and 36.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
49
Nitric Oxide 160 ppm
* Entire USA* The sponsor will provide air transportation and housing to patients that are not located in the area of clinical trial sites. All trial sites can treat adults.
Garden Grove, California, United States
Children's Hospital of Los Angeles (Adults can be treated here) (Site No. 500)
Los Angeles, California, United States
Nationwide Children's Hospital (Adults can be treated here) (Site No. 600)
Columbus, Ohio, United States
Change in FEV1 % predicted from baseline to Day 15
The primary efficacy variable for this study is absolute change from baseline FEV1% predicted to Day 15. For each subject, the change will be calculated as the FEV1% value minus the baseline FEV1%, i.e., a positive change in FEV1% values will indicate an increase in FEV1% after treatment. The primary endpoint for this trial is the comparison of the mean absolute change from baseline in FEV1% between treatment groups.
Time frame: 15 Days
Mean absolute change in FEV1% from baseline to Day 15 in the NO group (within group test).
Clinical Measurement of Mean absolute change in FEV1% from baseline to Day 15 in the NO group (within group test).
Time frame: 15 days
Mean change in prevalent recovered organisms' sputum CFU g (log 10) from baseline to Days 10, 15 and 36
Clinical Measurement of Mean change in prevalent recovered organisms' sputum CFU g (log 10) from baseline to Days 10, 15 and 36
Time frame: 36 days
Mean change in distance walked in the six-minute walk test from baseline to Days 15 and 36.
Clinical Measurement of Mean change in distance walked in the six-minute walk test from baseline to Days 15 and 36.
Time frame: 36 days
Mean absolute change in FEV1 % predicted from baseline to Days 10 and 36.
Clinical Measurement of Mean absolute change in FEV1 % predicted from baseline to Days 10 and 36.
Time frame: 36 days
Mean change in FEV1 % predicted (relative) from baseline to Days 10, 15, and 36.
Clinical Measurement of Mean change in FEV1 % predicted (relative) from baseline to Days 10, 15, and 36.
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Medical University of South Carolina (Site No. 200)
Charleston, South Carolina, United States
University of Washington Medical Center (Site No. 100)
Seattle, Washington, United States
Medical College of Wisconsin (Site No. 400)
Milwaukee, Wisconsin, United States
University of British Columbia, St. Paul's Hospital (Site No. 300)
Vancouver, B.C., Canada
Time frame: 36 days
Mean change in FVC from baseline to Days 10, 15 and 36
Clinical Measurement of Mean change in FVC from baseline to Days 10, 15 and 36
Time frame: 36 days
Mean change in FEF25-75 from baseline to Days 10, 15 and 36
Clinical Measurement of Mean change in FEF25-75 from baseline to Days 10, 15 and 36
Time frame: 36 days
Mean change in CFQ-R scores for each domain from baseline to Days 15 and 36
Clinical Measurement of Mean change in CFQ-R scores for each domain from baseline to Days 15 and 36
Time frame: 36 days
Counts of CFRSD-CRISS symptom scores for each symptom from evening prior to Day 1 to each day of the study (Days 1-35)
Clinical Measurement of Counts of CFRSD-CRISS symptom scores for each symptom from evening prior to Day 1 to each day of the study (Days 1-35)
Time frame: 35 days
Number of subjects with a relative improvement between baseline and Day 10 in FEV1 % predicted of ≥7.5%
Clinical Measurement of Number of subjects with a relative improvement between baseline and Day 10 in FEV1 % predicted of ≥7.5%
Time frame: 10 days
Number of subjects with an absolute improvement in CFQ-R survey scores ≥5 between baseline and Days 15 and 36
Clinical Measurement of Number of subjects with an absolute improvement in CFQ-R survey scores ≥5 between baseline and Days 15 and 36
Time frame: 36 days
Number of subjects with a positive response in the 6 minute walk test at Days 15 and 36
Clinical Measurement of Number of subjects with a positive response in the 6 minute walk test at Days 15 and 36
Time frame: 36 days