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Pulsed Inhaled Nitric Oxide for the Treatment of Patients With Mild or Moderate COVID-19

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ClinicalTrials.gov Identifier: NCT04358588
Expanded Access Status : No longer available
First Posted : April 24, 2020
Last Update Posted : June 12, 2020
Sponsor:
Information provided by (Responsible Party):
Bellerophon

Brief Summary:

The search for novel therapies to address the ongoing coronavirus (COVID-19) pandemic is ongoing. No proven therapies have been identified to prevent progression of the virus. Preliminary data suggest that inhaled nitric oxide (iNO) could have benefit in preventing viral progression and reducing reliance on supplemental oxygen and ventilator support.

Expanded access allows for iNO to be delivered via the portable INOpulse delivery system for the treatment of COVID-19.


Condition or disease Intervention/treatment
Coronavirus Infection COVID-19 Pneumonia, Viral Drug: iNO (inhaled nitric oxide) delivered via the INOpulse Delivery System

Detailed Description:

NO is a naturally produced molecule that is critical to the immune response to defend against pathogens and infections. In vitro studies have shown that NO inhibits the replication of severe acute respiratory syndrome-related coronavirus (SARS-CoV) and improves survival for cells infected with SARS-CoV. Additionally, in a clinical study of patients infected with SARS-CoV, iNO demonstrated improvements in arterial oxygenation, a reduction in ventilation support and an improvement in lung infiltrates observed on chest radiography. Based on the genetic similarities between the two coronaviruses, the data in SARS-CoV support the potential for iNO to provide meaningful benefit for patients infected with COVID-19.

The clinical spectrum of the COVID-19 infection ranges from mild signs of upper respiratory tract infection to severe pneumonia and death. Preventing disease progression in patients with mild or moderate disease would improve morbidity/mortality and significantly reduce the impact on limited healthcare resources.

Expanded access allows for iNO to be delivered via the INOpulse delivery system for the treatment of COVID-19. INOpulse technology provides targeted pulsatile delivery of iNO via portable INOpulse delivery system.

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Study Type : Expanded Access
Expanded Access Type : Intermediate-size Population
Official Title: Expanded Access: Pulsed, Inhaled Nitric Oxide (iNO) for the Treatment of Patients With Mild or Moderate Coronavirus Disease (COVID-19)



Intervention Details:
  • Drug: iNO (inhaled nitric oxide) delivered via the INOpulse Delivery System
    Patients will be treated by means of an INOpulse device and cannula. The active study drug, nitric oxide for inhalation (iNO), will be provided in size 0.074 liter aluminum cartridge at a concentration of 6.0 mg/L (4880 ppm).

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 95 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Criteria

Inclusion Criteria:

  1. Signed Informed Consent Form (and assent as appropriate) prior to the initiation of any study mandated procedures or assessments.
  2. At least 18 years old
  3. Patients with proven or high suspicion of SARS-CoV-2 infection and on supplemental oxygen ≤ 10 L/minute
  4. Suspected or proven pneumonia on chest imaging
  5. Female patients of childbearing potential must have a negative pre-treatment pregnancy test (serum or urine). All female patients should take adequate precaution to avoid pregnancy.
  6. Willing and able to comply with treatment schedule and study procedures.

Exclusion Criteria:

  1. Participating in any other clinical trial of an experimental treatment for COVID-19
  2. Gas exchange and ventilation requiring the use of any continuous positive airway pressure (CPAP), or any system of Non Invasive Ventilation (NIV), with Positive End-Expiratory Pressure (PEEP) ≤ 10 cmH2O prior to initiation of iNO
  3. Pregnancy, or positive pregnancy test in a pre-dose examination
  4. Open tracheostomy
  5. Clinical contra-indication, as deemed by the attending physician
  6. Use of a nitric oxide donor agent such as nitroglycerin or drugs known to increase methemoglobin such as lidocaine, prilocaine, benzocaine or dapsone at screening
  7. Known history or clinical evidence of heart failure, left ventricular dysfunction (LVEF < 40 %)
  8. Patients reporting hemoptysis

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04358588


Sponsors and Collaborators
Bellerophon
Investigators
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Study Director: Hunter Gilles, MD Acting Chief Medical Officer
Publications:
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Responsible Party: Bellerophon
ClinicalTrials.gov Identifier: NCT04358588    
Other Study ID Numbers: PULSE-EAP-001
First Posted: April 24, 2020    Key Record Dates
Last Update Posted: June 12, 2020
Last Verified: June 2020
Keywords provided by Bellerophon:
coronavirus
corona virus
COVID-19
COVID 19
SARS
SARS-coronavirus
Pneumonia
Pneumonia, viral
Virus
Additional relevant MeSH terms:
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Coronavirus Infections
Severe Acute Respiratory Syndrome
Pneumonia, Viral
Pneumonia
Lung Diseases
Respiratory Tract Diseases
Respiratory Tract Infections
Coronaviridae Infections
Nidovirales Infections
RNA Virus Infections
Virus Diseases
Nitric Oxide
Bronchodilator Agents
Autonomic Agents
Peripheral Nervous System Agents
Physiological Effects of Drugs
Anti-Asthmatic Agents
Respiratory System Agents
Free Radical Scavengers
Antioxidants
Molecular Mechanisms of Pharmacological Action
Neurotransmitter Agents
Endothelium-Dependent Relaxing Factors
Vasodilator Agents
Gasotransmitters
Protective Agents