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NCT03071692 · ClinicalTrials.gov registry record · Phase 3

Pemafibrate to Reduce Cardiovascular OutcoMes by Reducing Triglycerides IN patiENts With diabeTes (PROMINENT)

A Phase 3 study, sponsored by Kowa Research Institute.

Terminated
Registry status
Phase 3
Development phase
10,544
Enrollment target

NCT03071692: Clinical Trial Phase 3 study, sponsored by Kowa Research Institute.

NCT03071692 is a Phase 3 study that was terminated before completion, run by Kowa Research Institute. The registered enrollment target is 10,544 participants, above the 771-participant average among 15,282 other Phase 3 trials with a reported enrollment target (1268% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03071692, a Phase 3 study, was terminated before completion, sponsored by Kowa Research Institute.

TERMINATED
Registry status
Phase 3
Development phase
10,544 participants
Enrollment target

Study Summary

The primary objective of the study is to determine whether pemafibrate administered twice daily will delay the time to first occurrence of any component of the clinical composite endpoint of: * nonfatal Myocardial Infarction (MI) * nonfatal ischemic stroke * coronary revascularization; or * Cardio Vascular (CV) death.

Primary Outcome

Number of participants experiencing their first occurrence of any component of the 4-component composite primary endpoint, which includes nonfatal myocardial infarction (MI), nonfatal ischemic stroke, coronary revascularization, or cardiovascular (CV) death. Each participant is counted only once, regardless of any subsequent events.

Interventions

  • DRUG Placebo
  • DRUG K-877

Trial Details

FieldValue
Enrollment Target 10,544 participants
Start Date 2017-03-23
Est. Completion 2022-07-27
Phase Phase 3
Kowa Research Institute

44 total trials

Why NCT03071692 stopped before completion

NCT03071692 is an interventional study that assigns participants to a tested intervention. Its 10,544 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 (1268% higher).

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

NCT03071692 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03071692 about?

NCT03071692 is a clinical study titled "Pemafibrate to Reduce Cardiovascular OutcoMes by Reducing Triglycerides IN patiENts With diabeTes (PROMINENT)". The primary objective of the study is to determine whether pemafibrate administered twice daily will delay the time to first occurrence of any component of the clinical composite endpoint of: * nonfatal Myocardial Infarction (MI) * nonfatal ischemic stroke * coronary revascularization; or * Cardio ...

What is the current status of trial NCT03071692?

This trial is currently terminated. It is a Phase 3 study. The enrollment target is 10,544 participants. The study started on 2017-03-23. Estimated completion is 2022-07-27.

What interventions are being tested in trial NCT03071692?

The interventions under investigation include: Placebo (DRUG), K-877 (DRUG).

Who is sponsoring clinical trial NCT03071692?

This trial is sponsored by Kowa Research Institute, which has 44 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03071692's enrollment target sits among peer trials

10,544 25th of 2000 higher than 1,976 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 NCT03071692, the US trial registry maintained by the National Library of Medicine. NCT03071692 (large enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.