CovidResearchTrials by Shray Alag


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EtoposideWiki

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


Correlated Drug Terms (0)


Name (Synonyms) Correlation

Correlated MeSH Terms (1)


Name (Synonyms) Correlation
D007239 Infection NIH 0.08

Correlated HPO Terms (0)


Name (Synonyms) Correlation

There is one clinical trial.

Clinical Trials


1 A Phase II Single-Center, Open-Label, Safety and Efficacy Study of Etoposide in Patients With COVID-19 Infection

This is a single arm, open label study designed to evaluate the safety and efficacy of etoposide in patients with the 2019 novel coronavirus (COVID-19) infection. Treatment will be comprised of etoposide administered intravenously at a dose of 150 mg/m2 on Days 1 and 4 as prevention of cytokine storm in patients with COVID-19 infection.

NCT04356690 COVID-19 Drug: Etoposide
MeSH:Infection

Primary Outcomes

Description: An 8 point ordinal scale will be used to assess pulmonary status consisting of the following values: 8= Death; 7= Ventilation in addition to extracorporeal membrane oxygen (ECMO), continuous renal replacement therapy (CRRT), or need for vasopressors (dopamine ≥5 μg/kg/min OR epinephrine ≥0.1 μg/kg/min OR norepinephrine ≥0.1 μg/kg/min); 6= Intubation and mechanical ventilation; 5= Non-invasive mechanical ventilation (NIV) or high-flow oxygen; 4= Oxygen by mask or nasal prongs; 3= Hospitalization without oxygen supplementation; 2= Discharged from hospital either to home with supplemental oxygen OR to inpatient rehabilitation/skilled nursing facility (+/- supplemental oxygen); 1= Discharged to home without supplemental oxygen

Measure: Change in pulmonary status

Time: baseline, through study completion, an average of 45 days

Secondary Outcomes

Measure: Change in ferritin levels

Time: baseline, through study completion, an average of 45 days

Measure: Change in C-reactive protein levels

Time: baseline, through study completion, an average of 45 days

Measure: Change in d-dimer levels

Time: baseline, through study completion, an average of 45 days

Measure: Change in white blood cell count

Time: baseline, through study completion, an average of 45 days

Description: number of events

Measure: Incidence of serious adverse events

Time: baseline, through study completion, an average of 45 days

Measure: Overall survival

Time: Days 15, 30 and 60

Description: When calculating days of hospitalization, re-hospitalization or death occurring in the first 28 days should result in zero ascribed to time out of the hospital prior to readmission.

Measure: Length of hospitalization

Time: From date of enrollment until the date of extubation, assessed study completion, an average of 45 days

Measure: Duration of ventilation

Time: From date of enrollment until the date of extubation, assessed study completion, an average of 45 days

Description: Reintubations or death within 28 days will result in zero ascribed time off ventilator prior to reintubation

Measure: Ventilator free days

Time: baseline, through study completion, an average of 45 days

Measure: Improvement in arterial oxygen partial pressure (PaO2) to fractional inspired oxygen (FiO2)

Time: baseline, through study completion, an average of 45 days


No related HPO nodes (Using clinical trials)