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NCT01396590 · ClinicalTrials.gov registry record · Phase 1

Demonstrate Bioequivalence Between 6 ? 2-mg Tablets of Perampanel and a Single 12-mg Tablet of Perampanel in Healthy Subjects

A Phase 1 study of Healthy, sponsored by Eisai.

Completed
Registry status
Phase 1
Development phase
54
Enrollment target
1
Study location

NCT01396590 is a Phase 1 study of Healthy that has completed, run by Eisai. The registered enrollment target is 54 participants, below the 647-participant average among 1,090 other Healthy trials with a reported enrollment target (92% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT01396590, a Phase 1 study of Healthy, has completed, sponsored by Eisai.

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

Study Summary

The purpose of this study is to determine that six 2-mg tablets of perampanel are bioequivalent to one 12-mg tablet of perampanel.

Conditions Studied

Interventions

  • DRUG Perampanel

Study Locations (1)

North Dakota

  • - Fargo

Trial Details

FieldValue
Enrollment Target 54 participants
Start Date 2010-12
Est. Completion 2011-03
Phase Phase 1

Sponsor

Eisai

287 total trials

What the Registry Record Tells You About NCT01396590

The ClinicalTrials.gov registry entry for NCT01396590 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 54 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 647-participant average among 1,090 other Healthy trials with a reported enrollment target (92% lower). The listed sponsor is Eisai, which has 287 total studies on file at ClinicalTrials.gov.

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

NCT01396590 reports 1 study location spanning 1 distinct geographic area - top geographies include North Dakota.

Frequently Asked Questions

What is clinical trial NCT01396590 about?

NCT01396590 is a clinical study titled "Demonstrate Bioequivalence Between 6 ? 2-mg Tablets of Perampanel and a Single 12-mg Tablet of Perampanel in Healthy Subjects". The purpose of this study is to determine that six 2-mg tablets of perampanel are bioequivalent to one 12-mg tablet of perampanel.

What is the current status of trial NCT01396590?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 54 participants. The study started on 2010-12. Estimated completion is 2011-03.

What conditions does trial NCT01396590 study?

This clinical trial studies the following conditions: Healthy.

What interventions are being tested in trial NCT01396590?

The interventions under investigation include: Perampanel (DRUG).

Who is sponsoring clinical trial NCT01396590?

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

Where is trial NCT01396590 being conducted?

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

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.