Corona Virus Infection, Respiratory Tract Infections
Conditions
Keywords
inhaled nitric oxide, non tuberculous mycobacteria, drug resistant pneumonia, Burkholderia, Aspergillus, COVID-19, Viral Envelope Proteins, SARS-COV-2
Brief summary
Non tuberculous mycobacteria (NTM), Burkholdria spp, Aspergillus in the lung are almost impossible to eradicate with conventional antibiotics. In addition COVID-19 has know current treatment. These patients have few options to treat their lung infection. Nitric oxide has broad bactericidal and virucidal properties. It has been shown that nitric oxide was safe to be inhaled for similar cystic fibrosis patients and reduced drug resistant bacteria in the lungs. Further, research indicates that clinical isolates of NTM, Burkholderia spp, Aspergillus spp and Corona-like viruses can be eradicated by 160ppm NO exposure in the laboratory petri dish. This is not the first time inhaled NO treatment has been used in patients with difficult lung infections. This study will provide more data to see if NO therapy can reduce the bacterial load in the lungs, help the patients breath better; and in the case of COVID-19 act as a anti-viral agent resulting in the reduction of incidence of oxygen therapy, mechanical assistance of BIPAP, CPAP, intubation and mechanical ventilation during the study period.
Detailed description
Main Study Primary Objective: Assess the safety of inhaled NO (gNO) in adults & adolescents with NTM, Burkholderia, Aspergillus Lung Infections and Viral Lung (COVID-19) Infections Safety will be evaluated by unanticipated adverse events in clinical labs (hematology, coagulation, and serum chemistries); in vitals; in inspired concentration of NO, O2 and NO2 delivered to each subject and; in real time methemoglobin and oxygen saturation levels. Primary Endpoint: Determine the safety of gNO in the NTM population, * as confirmed by no unanticipated adverse events * Absence of a deleterious mean change in FEV1% predicted (absolute) from baseline Secondary safety Endpoint: Determine the efficacy of inhaled NO in adults with NTM, Burkholderia and Aspergillus Lung Infections Efficacy will be evaluated by measuring the change in lung function with spirometry (specifically absolute change in FEV1 % predicted) from baseline to Days 5, 12, 19 and 26. Secondary Efficacy Endpoint Determine the presence of an efficacy signal of gNO in the NTM, Burkholderia and Aspergillus Lung Infections Efficacy will be assessed by the antimicrobial effect of inhaled NO on the density of NTM species and other microorganisms in sputum. Serial measurements of these microbial colony counts in sputum have been previously used as a measure of antimicrobial activity in other clinical trials of antibiotics in NTM. • as confirmed by an improvement in pre-treatment bacterial colonization and post-treatment bacterial colonization on Days 19 and 26 as compared to baseline. Efficacy will be assessed by change in Quality of Life Score. * as assessed by an improvement in CRISS Score on Day 5, 19 and 26 as compared to baseline measurement; * as determined by improvement in six-minute walk test with one minute recovery as compared to baseline measurement. COVID-19 Substudy Primary Endpoint: Efficacy will be evaluated by measuring reduction in the incidence of mechanical assistance of BIPAP, CPAP, intubation and mechanical ventilation during the study period. Secondary Endpoints: 1. Proportion of patients with mild COVID2019 who deteriorate to a severe form of the disease requiring mechanical intervention like BIPAP/CPAP, intubation and mechanical ventilation; 2. Mortality from all causes during the study period; 3. Negative conversion of COVID-19 RT-PCR from upper respiratory tract measured as the proportion of patients with a negative conversion of RT-PCR from an oropharyngeal or a nasopahryngeal swab; 4. Time to clinical recovery defined as the time from initiation of the study to discharge or to normalization of fever (defined as \<36.6°C from axillary site, or \< 37.2°C from oral site or \< 37.8°C from rectal or tympanic site), respiratory rate (\< 24 bpm while breathing room air); 5. Alleviation of symptoms recorded in the Modified Jackson Cols score with particular definition of cough (defined as mild or absent in a patient reported scale of severity).
Interventions
DRUGNitric Oxide 0.5 % / Nitrogen 99.5 % Gas for Inhalation
Inhaled Nitric Oxide 160ppm balance air
Sponsors
Mallinckrodt
Chris Miller
Study design
Allocation
NA
Intervention model
SEQUENTIAL
Primary purpose
TREATMENT
Masking
NONE
Intervention model description
Open label safety study (COVID-19 Sub-study)
Eligibility
Sex/Gender
ALL
Age
19 Years to No maximum
Healthy volunteers
No
Inclusion criteria
COVID SubStudy Inclusion Criteria * Capable of understanding and providing signed informed consent and ability to adhere to the requirements and restrictions of this protocol; * Men and Women ≥ 19 years of age unless local laws dictate otherwise; * English speaking; * Suspected of exposure to SARS-CoV-2 with fatigue and at least a fever (\>37.90 C) or cough or sore throat or a positive swab for SAR-CoV-2 within 5 days of the of enrollment; * Must be willing to use an adequate form of contraception (or abstinence) from the time of the first dose with the IMP until after the last dose of IMP.
Exclusion criteria
* Prior Tracheostomy; * Concomitant treatment involving high flow nasal cannula; * Any clinical contraindications, as judged by the attending physician; * Mentally or neurologically disabled patients who are considered not fit to consent to their participation in the study; * Prior COVID-19 infection or a positive swab for SARS-CoV-2 greater than 5 days from enrollment; * Family members in the same household already on the study; * Hydroxychloroquine, colchicine and other experimental antiviral medications; * unwilling to practice a medically acceptable form of contraception from screening to Day 26 (acceptable forms of contraception: abstinence, hormonal birth control, intrauterine device, or barrier method plus a spermicidal agent). Recruitment on hold for following Criteria during COVID-19 Pandemic Inclusion Criteria: * Written informed consent. * Has been previously diagnosed with NTM, Burkholderia spp and Aspergillus spp. or Corona-like viral infection: 1. NTM, Burkholderia spp and Aspergillus spp defined as positive culture(s) of at least one species of Mycobacterium avium Complex (MAC) or Mycobacterium abscessus Complex (MABSCor Burkholderia spp and Aspergillus spp) or Corona-like viral infection: 2. History of repeatedly positive cultures (2 or more), irregardless of therapy * Male or female ≥14 years of age. * Female not pregnant at time of study. * Has an FEV1 ≥ 30 % of predicted. c. Suspected corona-like viral infection * Oxygen saturation on room air \>92% at screening. a. Able to breathe without supplemental oxygen for 60 minutes * Non-smoker for at least 6 months prior to screening and agrees not to smoke during the study. * Willing and able to comply with the treatment schedule and procedures.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Measure the safety of 160ppm inhaled nitric oxide delivery in NTM subjects | 26 Days | Measure the number of unanticipated adverse events over the duration of the study protocol |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Measure the effect of 160ppm inhaled nitric oxide delivery on lung spirometry in NTM subjects | Day 5,12,19 and 26 | Measure the change in absolute FEV1.0 change from baseline during 160 ppm inhalation therapy |
| Measure the antimicrobial effect of 160ppm inhaled nitric oxide on lung NTM bacterial load in the sputum | Day 19 and 26 | Measure the difference from baseline NTM species bacterial load (0 to +4) in sputum during 160ppm nitric oxide inhalation therapy |
| Measure the effect of 160ppm inhaled nitric oxide on Quality of Life (CRISS) Score | Day 19 and 26 | Measure the difference from baseline CRISS (0-100) during 160ppm nitric oxide inhalation therapy (lower score represents higher quality of life) |
Other
| Measure | Time frame | Description |
|---|---|---|
| Sub-Study Primary Endpoint(s): Efficacy to reduce respiratory interventions | Day 26 | Measuring reduction in the incidence of mechanical assistance including oxygen therapy, BIPAP, CPAP, intubation and mechanical ventilation during the study period. |
| Efficacy on the respiratory symptoms | Day 26 | Measured by change in the Modified Jackson Cold Score |
| Efficacy in reduction of mortality | Day 26 | Measured by death from all causes |
| Antiviral effect | Day 26 | Assessed by time to negative conversion of COVID-19 RT-PCR from upper respiratory tract |
| Efficacy on clinical improvement | Day 26 | Time to clinical recovery as measured by resolution of clinical signs |
Countries
Canada
Outcome results
None listed