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NCT02988115 · ClinicalTrials.gov registry record · Phase 3

Evaluation of the Efficacy and Safety of Bempedoic Acid (ETC-1002) in Patients With Hyperlipidemia and Statin Intolerant

A Phase 3 study, sponsored by Esperion Therapeutics.

Completed
Registry status
Phase 3
Development phase
345
Enrollment target

NCT02988115: Completed Phase 3 study, sponsored by Esperion Therapeutics.

NCT02988115 is a Phase 3 study that has completed, run by Esperion Therapeutics. The registered enrollment target is 345 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (55% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02988115, a Phase 3 study, has completed, sponsored by Esperion Therapeutics.

COMPLETED
Registry status
Phase 3
Development phase
345 participants
Enrollment target

Study Summary

The purpose of this study is to determine if bempedoic acid (ETC-1002) is effective and safe versus placebo in patients with elevated LDL cholesterol and who are statin-intolerant.

Primary Outcome

PCFB was calculated as the (\[post-Baseline (BL) value minus the BL value\] divided by the BL value ) x 100. BL was defined as the mean of the last two non-missing values on or prior to Day 1. If only one value was available, that single value was used as BL. PCFB in LDL-C was analyzed using analysis of covariance (ANCOVA), with treatment group and stratification factor (primary prevention; secondary prevention) as fixed effects and BL as a covariate. For participants with missing lipid data at

Interventions

  • OTHER placebo
  • DRUG bempedoic acid

Trial Details

FieldValue
Enrollment Target 345 participants
Start Date 2016-11-16
Est. Completion 2018-03-16
Phase Phase 3
Esperion Therapeutics

23 total trials

What the finished NCT02988115 record still lists

NCT02988115 is an interventional study that assigns participants to a tested intervention. The registered 345 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (55% lower).

The record links to 0 conditions, and to 2 interventions - of which placebo is the first listed.

NCT02988115 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02988115 about?

NCT02988115 is a clinical study titled "Evaluation of the Efficacy and Safety of Bempedoic Acid (ETC-1002) in Patients With Hyperlipidemia and Statin Intolerant". The purpose of this study is to determine if bempedoic acid (ETC-1002) is effective and safe versus placebo in patients with elevated LDL cholesterol and who are statin-intolerant.

What is the current status of trial NCT02988115?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 345 participants. The study started on 2016-11-16. Estimated completion is 2018-03-16.

What interventions are being tested in trial NCT02988115?

The interventions under investigation include: placebo (OTHER), bempedoic acid (DRUG).

Who is sponsoring clinical trial NCT02988115?

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 NCT02988115's enrollment target sits among peer trials

345 1050th of 2000 higher than 951 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 NCT02988115, the US trial registry maintained by the National Library of Medicine. NCT02988115 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.