CovidResearchTrials by Shray Alag


CovidResearchTrials Covid 19 Research using Clinical Trials (Home Page)


AT-001Wiki

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


Correlated Drug Terms (2)


Name (Synonyms) Correlation
drug2041 Recombinant human alkaline phosphatase Wiki 1.00
drug1822 Placebo Wiki 0.06

Correlated MeSH Terms (2)


Name (Synonyms) Correlation
D018805 Sepsis NIH 0.45
D058186 Acute Kidney Injury NIH 0.24

Correlated HPO Terms (2)


Name (Synonyms) Correlation
HP:0100806 Sepsis HPO 0.45
HP:0001919 Acute kidney injury HPO 0.24

There is one clinical trial.

Clinical Trials


1 A Single-center Registry and Embedded Interventional Study of the Effects of COVID-19 With and Without Treatment With AT-001 on Cardiac Structure and Function in Patients Hospitalized for Management of COVID-19 Infection

This is a prospective single-center registry with an embedded open-label single-arm clinical trial to determine the effects of standard of care treatment vs. standard of care plus AT-001 on cardiac structure and function and in-hospital survival in patients hospitalized for management of COVID-19 infection. Eligible subjects with COVID-19 infection will be identified at the time of hospital admission based on existing infection control surveillance protocols, and will have clinical data extracted from the electronic medical record to determine clinical characteristics associated with cardiac structure and function and in-hospital survival. A subset of patients with history of diabetes mellitus and/or acute hyperglycemia (any glucose measurement >126 mg/dl) and evidence of acute or chronic heart disease will be treated in an open-label fashion to receive an investigational aldose reductase inhibitor, AT-001 plus standard of care.

NCT04365699 COVID-19 Drug: AT-001

Primary Outcomes

Description: Primary Outcome Measure for overall Registry. All clinically-derived data will be collected on a daily basis until hospital discharge, or first 30 days of hospitalization (whichever is shorter).

Measure: Proportion of subjects with decreased left ventricular ejection fraction ≥10% from baseline at time of hospitalization

Time: 30 days

Description: Primary Outcome measure for Interventional Arm. All clinically-derived data will be collected on a daily basis during IP administration, with safety monitoring continuing 30 days after last dose of IP.

Measure: Incidence of Adverse Events for patients receiving AT-001

Time: 45 days

Secondary Outcomes

Description: Registry + Interventional

Measure: Change in left ventricular ejection fraction

Time: 30 days

Description: Registry + Interventional

Measure: Change in left ventricular end-diastolic diameter

Time: 30 days

Description: Registry + Interventional

Measure: Change in left ventricular end-systolic diameter

Time: 30 days

Description: Registry + Interventional

Measure: Change in biomarkers of cardiac injury

Time: 30 days

Description: Registry + Interventional

Measure: Frequency of atrial fibrillation

Time: 30 days

Description: Registry + Interventional

Measure: Frequency of heart block

Time: 30 days

Description: Registry + Interventional

Measure: Frequency of non-sustained ventricular tachycardia

Time: 30 days

Description: Registry + Interventional

Measure: Frequency of sustained ventricular tachycardia

Time: 30 days

Description: Registry + Interventional

Measure: Frequency of ventricular fibrillation

Time: 30 days

Description: Interventional patients only

Measure: Proportion of subjects requiring mechanical ventilation

Time: 30 days

Description: Interventional patients only

Measure: Proportion of subjects with decrease in left ventricular ejection fraction ≥10% from baseline at time of hospitalization

Time: 30 days


No related HPO nodes (Using clinical trials)