Clinical trial

Expanded Access: Pulsed, Inhaled Nitric Oxide (iNO) for the Treatment of Patients With Mild or Moderate Coronavirus Disease (COVID-19)

Name
PULSE-EAP-001
Description
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.
Trial arms
Treatment
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).
Size
-1
Eligibility 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
Protocol
{'studyType': 'EXPANDED_ACCESS', 'expandedAccessTypes': {'intermediate': True}}
Updated at
2023-02-21

1 organization

1 product

3 indications

Organization
Bellerophon
Product
iNO
Indication
COVID-19
Indication
Pneumonia
Indication
Viral