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NCT02089412 · ClinicalTrials.gov registry record · Phase 1

A Study to Determine the Effect of a High-Fat Meal on the Rate and Extent of E2006 Absorption in Healthy Subjects

A Phase 1 study of Healthy Subjects, sponsored by Eisai.

Completed
Registry status
Phase 1
Development phase
59
Enrollment target
1
Study location

NCT02089412: Completed Phase 1 study of Healthy Subjects, sponsored by Eisai.

NCT02089412 is a Phase 1 study of Healthy Subjects that has completed, run by Eisai. The registered enrollment target is 59 participants, below the 128-participant average among 69 other Healthy Subjects trials with a reported enrollment target (54% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02089412, a Phase 1 study of Healthy Subjects, has completed, sponsored by Eisai.

COMPLETED
Registry status
Phase 1
Development phase
59 participants
Enrollment target
1
Study location

Study Summary

This is an open-label, single-dose, randomized crossover study of single oral 10-mg tablet doses administered either after an overnight fast or in combination with a standard high-fat meal in healthy subjects.

Conditions Studied

Interventions

  • DRUG E2006

Study Locations (1)

Texas

  • PPD Development LLC - Austin

Trial Details

FieldValue
Enrollment Target 59 participants
Start Date 2014-02
Est. Completion 2014-06
Phase Phase 1
Eisai

287 total trials

What the finished NCT02089412 record still lists

NCT02089412 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 59 participants, a relatively small participant target, below the 128-participant average among 69 other Healthy Subjects trials with a reported enrollment target (54% lower).

The record links to 1 condition, with Healthy Subjects appearing as the primary indexed condition, and to 1 intervention - of which E2006 is the first listed.

NCT02089412 reports a single indexed study location in Texas.

Frequently Asked Questions

What is clinical trial NCT02089412 about?

NCT02089412 is a clinical study titled "A Study to Determine the Effect of a High-Fat Meal on the Rate and Extent of E2006 Absorption in Healthy Subjects". This is an open-label, single-dose, randomized crossover study of single oral 10-mg tablet doses administered either after an overnight fast or in combination with a standard high-fat meal in healthy subjects.

What is the current status of trial NCT02089412?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 59 participants. The study started on 2014-02. Estimated completion is 2014-06.

What conditions does trial NCT02089412 study?

This clinical trial studies the following conditions: Healthy Subjects.

What interventions are being tested in trial NCT02089412?

The interventions under investigation include: E2006 (DRUG).

Who is sponsoring clinical trial NCT02089412?

This trial is sponsored by Eisai, which has 287 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02089412 being conducted?

This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Healthy Subjects

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT02089412's enrollment target sits among peer trials

59 24th of 69 higher than 46 of 69 other Healthy Subjects trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Healthy Subjects 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 NCT02089412, the US trial registry maintained by the National Library of Medicine. NCT02089412 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.