Inhaled Sodium Nitrite as an Antimicrobial for Cystic Fibrosis
Primary Purpose
Cystic Fibrosis
Status
Active
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
sodium nitrite
Sponsored by
About this trial
This is an interventional treatment trial for Cystic Fibrosis
Eligibility Criteria
Inclusion Criteria:
- Cystic Fibrosis as documented by clinical features, and documentation of a positive sweat test or two disease causing mutation of the CF gene.
Exclusion Criteria:
- use of supplemental oxygen, FEV1 < 40% predicted, inability to discontinue inhaled antibiotics for 4 weeks,
- hospitalization within 4 weeks prior to enrollment,
- change in maintenance CF therapies within 4 weeks of enrollment,
- severe anemia, significant chronic liver disease, severe pulmonary hypertension, prior organ transplantation
Sites / Locations
- Children's Hospital of Pittsburgh
- Comprehensive Lung Center - Falk Clinic
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
sodium nitrite
Arm Description
Inhalation of 46 or 80 mg of sodium nitrite twice daily for four weeks
Outcomes
Primary Outcome Measures
Pulmonary Function
change in forced expiratory volume in one second (FEV1) after inhalation will assess safety
Secondary Outcome Measures
exhaled Nitric Oxide
concentration of nitric oxide in exhaled breath
sputum nitrite concentration
concentration of nitrite in sputum
Pseudomonas density in sputum
density of Pseudomonas in sputum
CF questionnaire - Respiratory
respiratory symptom questionnaire
Full Information
NCT ID
NCT02694393
First Posted
January 11, 2016
Last Updated
July 7, 2022
Sponsor
Schmidhofer, Mark, MD
Collaborators
Mast Therapeutics, Inc., Cystic Fibrosis Foundation
1. Study Identification
Unique Protocol Identification Number
NCT02694393
Brief Title
Inhaled Sodium Nitrite as an Antimicrobial for Cystic Fibrosis
Official Title
Phase I/II Study of Inhaled Sodium Nitrite as an Antimicrobial for Pseudomonas Infection in Cystic Fibrosis
Study Type
Interventional
2. Study Status
Record Verification Date
July 2022
Overall Recruitment Status
Active, not recruiting
Study Start Date
February 2016 (undefined)
Primary Completion Date
December 2022 (Anticipated)
Study Completion Date
April 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Schmidhofer, Mark, MD
Collaborators
Mast Therapeutics, Inc., Cystic Fibrosis Foundation
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This study will assess the safety of inhaled sodium nitrite in adults with Cystic Fibrosis and chronic Pseudomonas infections, and determine the ability of sodium nitrite to reduce the burden of Pseudomonas.
Detailed Description
Pseudomonas aeruginosa infects the airways of 80% of adults with Cystic Fibrosis (CF). In these patients, P. aeruginosa forms extremely antibiotic resistant biofilm communities that accelerate progression of obstructive lung disease. Current treatment of airway infection focuses on monthly cycles of inhaled antibiotics. However up to 20% of adults are infected with multi drug resistant P. aeruginosa for which we have no effective inhaled treatments. These isolates are more common as patients age so with the increasing life expectancy of the CF population, MDR P. aeruginosa is likely to remain a clinical problem. Another 10% of patients are infected with other Gram-negative organisms such as Burkholderia cepacia and Achromobacter species, for which we have inadequate suppressive treatment. Following lung transplant, MDR airway infections remain a problem as the allografts are colonized by strains carried in the paranasal sinuses. Sodium nitrite may present a new antimicrobial approach to treating respiratory infection with Gram-negative organisms, because it is able to prevent biotic biofilm formation.
Within the CF lung, P. aeruginosa grows as a biotic biofilm in association with airway epithelial cells and mucous plaques. This environment has an acidic pH and low oxygen tension with many bacteria subsisting through denitrification (both conditions where traditional antibiotics are less effective). Because biotic biofilms can be up to 500-fold more resistant than biofilms grown on abiotic surfaces, with support from our CF Research Development Program (RDP) Cores, we showed that nitrite prevents biofilm formation on the surface of primary CF airway epithelial cells. Moreover, nitrite dose-dependently potentiates the effects of colistin sulfate in liquid culture, and in biotic biofilms on airway epithelial cells. These data support the hypothesis that nebulized sodium nitrite will inhibit growth of Pseudomonas aeruginosa in CF airways, and identify a potential therapeutic benefit for nitrite alone and cooperatively with colistin as a novel therapy to inhibit P. aeruginosa in CF airways. Nebulized nitrite has been through extensive animal toxicology, and is well tolerated by subjects with pulmonary arterial hypertension where it is being studied as a pulmonary vasodilator.
To determine the therapeutic potential of sodium nitrite for CF, we propose two specific aims:
Aim 1: Determine the safety of nebulized sodium nitrite administered in two doses to patients with CF.
Aim 2: Explore the effects of inhaled sodium nitrite on measures of lung function, exhaled airway nitric oxide, and bacterial burden as measured by quantitative sputum cultures.
To accomplish these aims, we propose a Phase I/II open-label study of sodium nitrite in CF. Key inclusion criteria include individuals over the age 18 with cystic fibrosis as documented by clinical features of CF, and genotyping or a positive sweat test. Exclusion criteria include advanced lung disease, inability to discontinue inhaled antibiotics for four weeks, hospitalization or medication change within 4 weeks of enrollment, baseline systemic hypotension (SBP<90 mm hg), chronic kidney disease (Cr >2.5), severe anemia (Hgb <9 gm/dL in the last six months). The primary outcome is safety, defined as FEV1 measured before and after initial doses on days 0 and 7, and at week 4. Other safety data for the initial doses include pulse oximetry and transcutaneous methemoglobin levels. Secondary endpoints include quantitative sputum cultures, exhaled nitric oxide, sputum nitrite concentration, and patient symptoms as assessed by a CF specific respiratory questionnaire.
Completion of this study will guide the development of sodium nitrite as a single agent for CF infections, and inform future studies examining the effects of sodium nitrite in combination with inhaled colistin for patients with drug resistant bacterial pathogens that are an increasing problem. In addition, the study will provide important safety and efficacy data that may inform future development of inhaled sodium nitrite as a therapy in young patients to augment airway host defense and prevent biofilm formation.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cystic Fibrosis
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
35 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
sodium nitrite
Arm Type
Experimental
Arm Description
Inhalation of 46 or 80 mg of sodium nitrite twice daily for four weeks
Intervention Type
Drug
Intervention Name(s)
sodium nitrite
Other Intervention Name(s)
AIR001
Intervention Description
inhalation of 46 or 80 mg of sodium nitrite by electronic nebulization
Primary Outcome Measure Information:
Title
Pulmonary Function
Description
change in forced expiratory volume in one second (FEV1) after inhalation will assess safety
Time Frame
three times over 4 weeks (Day 0, Day 7, and Week 4)
Secondary Outcome Measure Information:
Title
exhaled Nitric Oxide
Description
concentration of nitric oxide in exhaled breath
Time Frame
three times over 4 weeks (Day 0, Day 7, and Week 4)
Title
sputum nitrite concentration
Description
concentration of nitrite in sputum
Time Frame
three times over 4 weeks (Day 0, Day 7 and Week 4)
Title
Pseudomonas density in sputum
Description
density of Pseudomonas in sputum
Time Frame
two times over 4 weeks (Day 0 and Week 4)
Title
CF questionnaire - Respiratory
Description
respiratory symptom questionnaire
Time Frame
two times over 4 weeks (Day 0 and Week 4)
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Cystic Fibrosis as documented by clinical features, and documentation of a positive sweat test or two disease causing mutation of the CF gene.
Exclusion Criteria:
use of supplemental oxygen, FEV1 < 40% predicted, inability to discontinue inhaled antibiotics for 4 weeks,
hospitalization within 4 weeks prior to enrollment,
change in maintenance CF therapies within 4 weeks of enrollment,
severe anemia, significant chronic liver disease, severe pulmonary hypertension, prior organ transplantation
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Joseph Pilewski, MD
Organizational Affiliation
University of Pittsburgh
Official's Role
Principal Investigator
Facility Information:
Facility Name
Children's Hospital of Pittsburgh
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15213
Country
United States
Facility Name
Comprehensive Lung Center - Falk Clinic
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15213
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
20696868
Citation
Major TA, Panmanee W, Mortensen JE, Gray LD, Hoglen N, Hassett DJ. Sodium nitrite-mediated killing of the major cystic fibrosis pathogens Pseudomonas aeruginosa, Staphylococcus aureus, and Burkholderia cepacia under anaerobic planktonic and biofilm conditions. Antimicrob Agents Chemother. 2010 Nov;54(11):4671-7. doi: 10.1128/AAC.00379-10. Epub 2010 Aug 9.
Results Reference
background
PubMed Identifier
25229185
Citation
Zemke AC, Shiva S, Burns JL, Moskowitz SM, Pilewski JM, Gladwin MT, Bomberger JM. Nitrite modulates bacterial antibiotic susceptibility and biofilm formation in association with airway epithelial cells. Free Radic Biol Med. 2014 Dec;77:307-16. doi: 10.1016/j.freeradbiomed.2014.08.011. Epub 2014 Sep 16.
Results Reference
background
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Inhaled Sodium Nitrite as an Antimicrobial for Cystic Fibrosis
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