Phase 2
N=36
Safety and Efficacy of Sildenafil in Cystic Fibrosis (CF) Lung Disease
Cystic Fibrosis
Bottom Line
View on ClinicalTrials.gov: NCT00659529 ↗Enrolled (actual)
36
Serious AEs
7.4%
Results posted
May 2014
Primary outcome: Primary: Change in Sputum Elastase Activity — -57 micrograms/mL
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 2
- Interventions
- sildenafil (Drug)
- Age
- Pediatric, Adult, Older Adult · 14+ yrs
- Sex
- All
- Sponsor
- National Jewish Health
- Primary completion
- Aug 2012
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Change in Sputum Elastase Activity |
-57 | — |
| SECONDARY Change in Exhaled Breath Condensate pH |
-0.09 | — |
| SECONDARY Change in Cystic Fibrosis Questionnaire - Revised (CFQ-R) Respiratory Domain, Average Unit Change From Baseline to 6 Weeks is Reported |
0.3 | — |
Summary
The purpose of this study is to determine whether sildenafil can decrease inflammation in CF lung disease.
Eligibility Criteria
Inclusion Criteria
- Confirmed diagnosis of CF based on the following criteria:
- Positive sweat chloride ≥60mEq/liter (by pilocarpine iontophoresis) and/or
- Genotype with two identifiable mutations consistent with CF, and accompanied by one or more clinical features consistent with the CF phenotype
- Male or female patients ≥ 12 years of age
- FEV1 ≥ 50% predicted (Knudson) 31
- Clinically stable without evidence of acute upper or lower respiratory tract infection or current pulmonary exacerbation within the 14 days prior to the screening visit
- Ability to reproducibly perform spirometry (according to ATS criteria)
- Ability to produce at least 1mL of sputum spontaneously, or be willing to undergo sputum induction
- Ability to understand and sign a written informed consent or assent and comply with the requirements of the study
- Chronic bacterial colonization (3 documented positive cultures in the prior 2 years of which at least one was obtained in the 3 months prior to randomization)
Exclusion Criteria
- History of hypersensitivity to sildenafil
- Use of an investigational agent within the 4-week period prior to Visit 1 (Day 0)
- Breastfeeding, pregnant, or verbal expression of unwillingness to practice an acceptable birth control method (abstinence, hormonal or barrier methods, partner sterilization or intrauterine device) during participation in the study
- Daily use of systemic corticosteroids and/or NSAIDs within 4 weeks of the study or as needed use within 72 hours prior to the screening visit
- History of significant hepatic (SGOT or SGPT > 3 times the upper limit of normal at screening, documented biliary cirrhosis, or portal hypertension), cardiovascular (history of aortic stenosis, coronary artery disease, pulmonary hypertension with right ventricular systolic pressure >55 mmHg or life-threatening arrhythmia), neurological (history of stroke), hematologic (history of bleeding diathesis), ophthalmologic (history of retinal impairment or non-arteritic ischemic optic neuritis) or renal impairment (creatinine >1.8 mg/dL.)
- Inability to swallow pills
- Previous lung transplantation
- Use of concomitant nitrates, α-blocker, or Ca channel blocker
- Use of concomitant medications known to be potent inhibitors of CYP3A4 (e.g. ketoconazole, itraconazole, ritonavir, clarithromycin, erythromycin, rifampin)
- Presence of a condition or abnormality that in the opinion of the investigator would compromise the safety of the subject or the quality of the data
- Weight less than 40 kg
- History of sputum or throat swab culture yielding Burkholderia cepacia within 2 years of screening
- Resting room air oxygen saturation <93%
- History of migraines
Data sourced from ClinicalTrials.gov (NCT00659529). 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.