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Inhaled Sodium Nitrite as an Antimicrobial for Cystic Fibrosis

Phase I/II Study of Inhaled Sodium Nitrite as an Antimicrobial for Pseudomonas Infection in Cystic Fibrosis

Status
Terminated
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02694393
Enrollment
4
Registered
2016-02-29
Start date
2016-02-29
Completion date
2022-07-21
Last updated
2024-06-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cystic Fibrosis

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.

Interventions

DRUGsodium nitrite

inhalation of 46 or 80 mg of sodium nitrite by electronic nebulization

Sponsors

Mast Therapeutics, Inc.
CollaboratorINDUSTRY
Cystic Fibrosis Foundation
CollaboratorOTHER
Schmidhofer, Mark, MD
Lead SponsorINDIV

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Pulmonary FunctionDay 7forced expiratory volume in one second (FEV1) after inhalation will assess safety

Secondary

MeasureTime frameDescription
Exhaled Nitric OxideDay 7concentration of nitric oxide in exhaled breath
Sputum Nitrite Concentrationday 7concentration of nitrite in sputum
Pseudomonas Density in Sputumday 28density of Pseudomonas in sputum
CF Questionnaire - Respiratoryday 28respiratory symptom questionnaire

Countries

United States

Participant flow

Pre-assignment details

The study had a 2 week wash-out period during which inhaled antibiotics were held before the drug was dosed. If participants had a drop in percent predicted FEV1 between the screening visit and Visit 1 where the drug was dosed, they were excluded from the study. Of our 4 enrolled subjects, 1 subject withdrew from study participation during the washout period and 1 subject failed the wash-out period and was excluded from the study before being assigned to treatment arm.

Participants by arm

ArmCount
Sodium Nitrite
Inhalation of 46 or 80 mg of sodium nitrite twice daily for four weeks sodium nitrite: inhalation of 46 or 80 mg of sodium nitrite by electronic nebulization
2
Total2

Baseline characteristics

CharacteristicSodium Nitrite
Age, Categorical
<=18 years
0 Participants
Age, Categorical
>=65 years
0 Participants
Age, Categorical
Between 18 and 65 years
2 Participants
Age, Continuous25.5 years
exhaled Nitric Oxide6.5 Parts per billion
FEV1 (Percent predicted)61.5 Percent predicted FEV1
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants
Race (NIH/OMB)
Asian
0 Participants
Race (NIH/OMB)
Black or African American
0 Participants
Race (NIH/OMB)
More than one race
0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants
Race (NIH/OMB)
White
2 Participants
Region of Enrollment
United States
2 participants
Sex: Female, Male
Female
0 Participants
Sex: Female, Male
Male
2 Participants

Adverse events

Event typeEG000
affected / at risk
deaths
Total, all-cause mortality
0 / 2
other
Total, other adverse events
2 / 2
serious
Total, serious adverse events
0 / 2

Outcome results

Primary

Pulmonary Function

forced expiratory volume in one second (FEV1) after inhalation will assess safety

Time frame: Day 7

ArmMeasureValue (MEAN)
Nebulized NitritePulmonary Function59 percentage of predicted FEV1
Primary

Pulmonary Function

forced expiratory volume in one second (FEV1) after inhalation will assess safety

Time frame: Day 28

ArmMeasureValue (NUMBER)
Nebulized NitritePulmonary Function78 percentage of predicted FEV1
Secondary

CF Questionnaire - Respiratory

respiratory symptom questionnaire

Time frame: day 28

Population: respiratory symptom questionnaire data not collected/measured

Secondary

Exhaled Nitric Oxide

concentration of nitric oxide in exhaled breath

Time frame: Day 7

ArmMeasureValue (MEAN)
Nebulized NitriteExhaled Nitric Oxide10 parts per billion
Secondary

Exhaled Nitric Oxide

concentration of nitric oxide in exhaled breath

Time frame: Day 28

ArmMeasureValue (NUMBER)
Nebulized NitriteExhaled Nitric Oxide12 parts per billion
Secondary

Pseudomonas Density in Sputum

density of Pseudomonas in sputum

Time frame: day 28

Population: Pseudomonas density in sputum data not collected/measured

Secondary

Sputum Nitrite Concentration

concentration of nitrite in sputum

Time frame: day 28

Population: Sputum nitrite data not collected/measured

Secondary

Sputum Nitrite Concentration

concentration of nitrite in sputum

Time frame: day 7

Population: Sputum nitrite data not collected/measured

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026