There is one clinical trial.
The purpose of this study is to determine whether XPro1595 can prevent the progression of
respiratory complications in COVID19 patients.
Primary Outcomes
Description: Disease progression is defined by the development of need for mechanical ventilation or death. Mechanical ventilation includes CPAP, BIPAP or mechanical ventilation requiring intubation.
Measure: Proportion of participants with disease progression from randomization to 28 days post-randomization
Time: 28 days
Secondary Outcomes
Measure: Proportion of participants with all-cause mortality Time: 28 days
Measure: Proportion of participants who transfer to ICU level care by Day 28 (ICU level care is defined as a hospital setting where patient to nurse ratio is < 4); Time: 28 days
Measure: Proportion of participants with a new onset of neurologic disease (requiring medical intervention), including stroke by Day 28; Time: 28 days
Measure: Proportion of participants with evidence of new CHF or new MI requiring medical intervention by Day 28; Time: 28 days
Measure: Proportion of participants with a new onset embolus or thrombus by Day 28; Time: 28 days
Measure: Proportion of participants who develop a need for renal replacement therapy (defined as need for any type of dialysis including intermittent or continuous peritoneal or hemodialysis) by Day 28; Time: 28 days
Measure: Proportion of participants with an increase in the WHO Ordinal Scale of Clinical Improvement score at any time during the study; Time: 28 days
Measure: Length of hospital stay defined as the number of days in hospital from time of randomization to time of discharge or death, whichever occurs first; Time: 28 days
Measure: Change from baseline in inflammation markers over time. Time: 28 days
Other Outcomes
Measure: Incidence of adverse events and serious adverse events not due to underlying disease Time: 28 days
Measure: Incidence of abnormal findings in clinical safety laboratory parameters, vital signs, and ECGs. Time: 28 days