Aerosoliserat DNase for Treatment of Respiratory Failure in Severe COVID-19

Study objectives: Primary objective: To compare the treatment effect of aerosolized DNase I to that of placebo (NaCl, 0.9%) on time to cessation of oxygen therapy or discharge from hospital in hospitalized patients with COVID-19 and respiratory dysfunction.

Secondary objectives: To compare the treatment effect of aerosolized DNase I to that of placebo (NaCl, 0.9%) on 28-day mortality, days alive and without ventilator treatment, days alive and without high flow nasal oxygen treatment (Optiflow), length of stay in the ICU, days alive and outside hospital, relapse of hypoxia, days alive and without need for supplemental oxygen, adverse reactions.

Exploratory objectives: To compare the treatment effect of aerosolized DNase I to that of placebo (NaCl, 9%) on quantification of NETs in respiratory secretions and on the incidence of clinical thromboembolic events.

Study design: Phase 2 open-label randomized controlled multicentre trial. The study period is 28 days from randomization. A long term follow-up on mortality and readmission will also be collected via patient medical records/registries at day 90, day 180, and day 360 after randomization.

Inclusion criteria

• Age ≥18 years old
• Admitted to hospital ward or ICU
• A positive PCR test for SARS-CoV-2 from throat swab or nasopharynx
• An oxygen saturation ≤90% after maximum 15 minutes without supplemental oxygen
• Signed informed consent

Exclusion criteria

• Mental inability, reluctance or language difficulties that result in difficulty understanding the meaning of study participation
• Known or suspected allergy against Pulmozyme
• Chronic obstructive pulmonary disease stage III-IV or another comparable chronic respiratory disease
• Participation in a clinical study with an investigational product during the last 30 days
• Previous participation in this study
• Pregnancy. Women of childbearing potential must agree to use contraceptives for the duration of the study period
• Any condition that, in the opinion of the Investigator, would place the patient at increased risk or preclude the patient's compliance with the study