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NCT01260155 · ClinicalTrials.gov registry record · Phase 1

A Single-Center, Open-Label, Randomized, 3-Treatment Crossover Bioavailability Study of Single Oral Doses of E5501 Old Tablet Formulation Under Fasted Conditions and a New Tablet Formulation Under Fed and Fasted Conditions in Healthy Subjects

A Phase 1 study, sponsored by Eisai.

Completed
Registry status
Phase 1
Development phase
16
Enrollment target

NCT01260155 is a Phase 1 study that has completed, run by Eisai. The registered enrollment target is 16 participants.

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The verdict

NCT01260155, a Phase 1 study, has completed, sponsored by Eisai.

COMPLETED
Registry status
Phase 1
Development phase
16 participants
Enrollment target

Study Summary

This study will be a single-center, open-label, randomized, 3-treatment crossover bioavailability study of single oral doses of E5501 old tablet formulation under fasted conditions and a new tablet formulation administered under fed and fasted conditions in healthy subjects.

Interventions

  • DRUG E5501

Trial Details

FieldValue
Enrollment Target 16 participants
Start Date 2010-01
Est. Completion 2010-06
Phase Phase 1

Sponsor

Eisai

287 total trials

What the Registry Record Tells You About NCT01260155

The ClinicalTrials.gov registry entry for NCT01260155 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 16 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Eisai, which has 287 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which E5501 is the first listed.

NCT01260155 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01260155 about?

NCT01260155 is a clinical study titled "A Single-Center, Open-Label, Randomized, 3-Treatment Crossover Bioavailability Study of Single Oral Doses of E5501 Old Tablet Formulation Under Fasted Conditions and a New Tablet Formulation Under Fed and Fasted Conditions in Healthy Subjects". This study will be a single-center, open-label, randomized, 3-treatment crossover bioavailability study of single oral doses of E5501 old tablet formulation under fasted conditions and a new tablet formulation administered under fed and fasted conditions in healthy subjects.

What is the current status of trial NCT01260155?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 16 participants. The study started on 2010-01. Estimated completion is 2010-06.

What interventions are being tested in trial NCT01260155?

The interventions under investigation include: E5501 (DRUG).

Who is sponsoring clinical trial NCT01260155?

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

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.