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Phase 2 N=36 Treatment

Safety and Efficacy of Sildenafil in Cystic Fibrosis (CF) Lung Disease

Cystic Fibrosis

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

OutcomeResultp-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
View full record on ClinicalTrials.gov →

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.

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