The Safety and Preliminary Tolerability of Lyophilized Lucinactant in Adults With Coronavirus Disease 2019 (COVID-19)

Windtree Therapeutics

Status and phase

Completed

Phase 2

Conditions

COVID-19

Acute Lung Injury/Acute Respiratory Distress Syndrome (ARDS)

Treatments

Drug: Lucinactant

Study type

Interventional

Funder types

Industry

Identifiers

NCT04389671

02-CL-2001a

Details and patient eligibility

About

This is a multicenter, single-treatment study. Subjects will consist of adults with COVID-19 associated acute lung injury who are being cared for in a critical care environment.

Full description

This is a multicenter, single-treatment study. Subjects will consist of adults with COVID-19 associated acute lung injury who are being cared for in a critical care environment.

Lucinactant is a synthetic surfactant that, in its liquid form (SURFAXIN®), is approved by the United States Food and Drug Administration (NDA 021746) for the prevention of respiratory distress syndrome (RDS) in premature infants at high risk for RDS.

It has been studied in over 2000 children and adults. Preliminary data from animal and adult human studies indicate that lucinactant may be able to benefit those with acute respiratory distress syndrome (ARDS) in the context of COVID-19 infection, improving oxygenation and lung compliance. When given to intubated patients, Lucinactant could potentially decrease the duration of ventilation.

Lucinactant has an extensive safety profile in different patient populations for different indications.

It is hypothesized that lucinactant may improve the respiratory status of patients suffering from COVID-19.

Enrollment

20 patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Signed and dated informed consent form (ICF) by the subject or legally authorized representative;
Age 18-75 (inclusive);
Assay positive for Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) virus, preferably by polymerase chain reaction (PCR);
Endotracheal intubation and mechanical ventilation (MV), within 7 days of initial intubation;
In-dwelling arterial line;
PaO2/FiO2 (P/F) ratio < 300;
Mean blood pressure ≥ 65 mmHg, immediately before enrollment;
Bilateral infiltrates seen on frontal chest radiograph.

Exclusion criteria

Life expectancy < 48 hours or do not resuscitate orders;
Severe lung disease (home O2, forced expiratory volume at one second [FEV1] < 2 liters) not likely to respond to therapy or profound hypoxemia (ie, oxygen index [OI] ≥ 25 or P/F ratio < 100);
Severe renal impairment (creatinine clearance < 30 mL/min);
Within the last 6 months has received, or is currently receiving, immunosuppression therapy (azathioprine, cyclophosphamide or methotrexate) or any transplant recipient;
Clinically significant cardiac disease that adversely effects cardiopulmonary function:
1. Acute coronary syndromes or active ischemic heart disease (as assessed by the PI using troponin and ECG)
2. Cardiac ejection fraction < 40% (if known);
3. Need for multiple-dose vasopressors to support blood pressure (single dose vasopressors, such as Levophed™ ≤ 0.1 mcg/kg/min are allowed);
4. Cardiogenic pulmonary edema as the etiology of the current respiratory distress;
5. Evidence of myocarditis or pericarditis;
Neuromuscular disease;
Neutropenia (ANC < 1000);
Active malignancy that impacts treatment decisions or life expectancy related to the trial;
Suspected concomitant bacterial or other viral lung infection. Bacterial infection defined as white blood count (WBC) > 15k and positive blood/urine/sputum culture results within 72 hours.