CovidResearchTrials by Shray Alag


CovidResearchTrials Covid 19 Research using Clinical Trials (Home Page)


XPro1595Wiki

Developed by Shray Alag
Clinical Trial MeSH HPO Drug Gene SNP Protein Mutation


Correlated Drug Terms (1)


Name (Synonyms) Correlation
drug1822 Placebo Wiki 0.06

Correlated MeSH Terms (1)


Name (Synonyms) Correlation
D018352 Coronavirus Infections NIH 0.04

Correlated HPO Terms (0)


Name (Synonyms) Correlation

There is one clinical trial.

Clinical Trials


1 A Multicenter, Double-Blind, Randomized, Placebo-Controlled Trial of XPro1595 in the Treatment of Participants With Pulmonary Complications From Coronavirus Disease (COVID-19)

The purpose of this study is to determine whether XPro1595 can prevent the progression of respiratory complications in COVID19 patients.

NCT04370236 COVID-19 Drug: XPro1595 Drug: Placebo

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


No related HPO nodes (Using clinical trials)