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Icosapent ethyl (IPE)Wiki

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


Correlated Drug Terms (2)


Name (Synonyms) Correlation
drug784 Doctor Spot Wiki 1.00
drug1822 Placebo Wiki 0.06

Correlated MeSH Terms (4)


Name (Synonyms) Correlation
D021821 Communicable Diseases, Emerging NIH 1.00
D004630 Emergencies NIH 0.19
D003141 Communicable Diseases NIH 0.09
D007239 Infection NIH 0.06

Correlated HPO Terms (0)


Name (Synonyms) Correlation

There is one clinical trial.

Clinical Trials


1 PREPARE-IT. Prevention of COVID19 With EPA in Healthcare Providers at Risk - Intervention Trial

The PREPARE-IT trial is a simple, pragmatic and universally applicable strategy with icosapent ethyl (IPE) at high doses intended to reduce infection rate and subsequent morbidity and mortality among subjects at high risk of infection due to COVID-19.

NCT04460651 COVID19 Drug: Icosapent ethyl (IPE) Drug: Placebo

Primary Outcomes

Description: SARS-CoV-2 positive subjects are defined as subjects with positive tests for SARS-CoV-2 RT-PCR or for SARS-CoV-2 lgG antibodies after developing COVID-19 disease at any stage within the follow-up period (including those subjects with or without symptomatic COVID-19 evaluated before the final visit) or those individuals who test positive for SARS-CoV-2 RT-PCR or for SARS-CoV-2 lgG antibodies at the final visit (day 60).

Measure: Percentage of SARS-CoV-2 positive subjects

Time: 60 days

Measure: Highest mean WHO descriptive score of COVID-19 in the active treatment group compared to the placebo group.

Time: 60 days

Secondary Outcomes

Measure: Highest mean WHO score up to day 60 for the active treatment group as compared to placebo among subjects with a positive test received at any moment during the study after the first visit

Time: 60 days

Description: Mean change from baseline will be computed

Measure: Total cholesterol, LDL, HDL, triglycerides (mg/dL) at baseline and at day 60

Time: baseline, 60 days

Description: Mean change from baseline will be computed

Measure: Ultrasensitive C-reactive Protein (mg/dL) at baseline and at day 60

Time: baseline, 60 days

Measure: Difference in hospital length of stay between groups

Time: 60 days

Measure: Difference in duration of mechanical ventilation in both groups

Time: 60 days

Measure: Rate of hospital admissions due to SARS (Severe Acute Respiratory Syndrome) in patients who were negative for SARS CoV-2 upon admission

Time: 60 days

Measure: Mean highest WHO descriptive score in active treatment versus placebo groups up to day 60 among hospitalized patients (WHO grades 3 or more) without serum evidence / PCR detecting SARS-CoV-2 infection

Time: 60 days

Measure: Rate of total events, non-fatal myocardial infarction or non-fatal stroke or death (initial and subsequent), up to day 60

Time: 60 days


No related HPO nodes (Using clinical trials)