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NCT02993406 · ClinicalTrials.gov registry record · Phase 3

Evaluation of Major Cardiovascular Events in Participants With, or at High Risk for, Cardiovascular Disease Who Are Statin Intolerant Treated With Bempedoic Acid (ETC-1002) or Placebo

A Phase 3 study, sponsored by Esperion Therapeutics.

Completed
Registry status
Phase 3
Development phase
13,970
Enrollment target

NCT02993406: Completed Phase 3 study, sponsored by Esperion Therapeutics.

NCT02993406 is a Phase 3 study that has completed, run by Esperion Therapeutics. The registered enrollment target is 13,970 participants, above the 771-participant average among 15,282 other Phase 3 trials with a reported enrollment target (1712% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02993406, a Phase 3 study, has completed, sponsored by Esperion Therapeutics.

COMPLETED
Registry status
Phase 3
Development phase
13,970 participants
Enrollment target

Study Summary

The purpose of this study is to determine if treatment with bempedoic acid (ETC-1002) versus placebo decreases the risk of cardiovascular events in participants who have or are at high risk for cardiovascular disease and are statin intolerant.

Primary Outcome

The primary efficacy end point was a four-component composite of adjudicated MACE, defined as death from cardiovascular causes, nonfatal myocardial infarction, nonfatal stroke, or coronary revascularization, as assessed in a time-to first-event analysis.

Interventions

  • DRUG Bempedoic acid 180 mg tablet
  • DRUG Matching placebo tablet

Trial Details

FieldValue
Enrollment Target 13,970 participants
Start Date 2016-12-22
Est. Completion 2022-11-07
Phase Phase 3
Esperion Therapeutics

23 total trials

What the finished NCT02993406 record still lists

NCT02993406 is an interventional study that assigns participants to a tested intervention. Its 13,970 participants enrollment target places it among the larger protocols in the corpus, above the 771-participant average among 15,282 other Phase 3 trials with a reported enrollment target (1712% higher).

The record links to 0 conditions, and to 2 interventions - of which Bempedoic acid 180 mg tablet is the first listed.

NCT02993406 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02993406 about?

NCT02993406 is a clinical study titled "Evaluation of Major Cardiovascular Events in Participants With, or at High Risk for, Cardiovascular Disease Who Are Statin Intolerant Treated With Bempedoic Acid (ETC-1002) or Placebo". The purpose of this study is to determine if treatment with bempedoic acid (ETC-1002) versus placebo decreases the risk of cardiovascular events in participants who have or are at high risk for cardiovascular disease and are statin intolerant.

What is the current status of trial NCT02993406?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 13,970 participants. The study started on 2016-12-22. Estimated completion is 2022-11-07.

What interventions are being tested in trial NCT02993406?

The interventions under investigation include: Bempedoic acid 180 mg tablet (DRUG), Matching placebo tablet (DRUG).

Who is sponsoring clinical trial NCT02993406?

This trial is sponsored by Esperion Therapeutics, which has 23 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02993406's enrollment target sits among peer trials

13,970 17th of 2000 higher than 1,984 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02993406, the US trial registry maintained by the National Library of Medicine. NCT02993406 (large enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.