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NCT01266590 · ClinicalTrials.gov registry record · Phase 1

A Study of LY2216684 and Digoxin in Healthy Subjects

A Phase 1 study of Major Depressive Disorder, sponsored by Eli Lilly and Company.

Completed
Registry status
Phase 1
Development phase
30
Enrollment target
1
Study location

NCT01266590 is a Phase 1 study of Major Depressive Disorder that has completed, run by Eli Lilly and Company. The registered enrollment target is 30 participants, below the 377-participant average among 282 other Major Depressive Disorder trials with a reported enrollment target (92% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT01266590, a Phase 1 study of Major Depressive Disorder, has completed, sponsored by Eli Lilly and Company.

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

Study Summary

The purpose of this study is to determine how much digoxin gets into the blood stream and how long it takes the body to get rid of it when given with LY2216684. Information about any side effects that may occur will also be collected.

Conditions Studied

Interventions

  • DRUG Digoxin
  • DRUG LY2216684

Study Locations (1)

Florida

  • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician. - Daytona Beach

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2010-12
Est. Completion 2011-02
Phase Phase 1

Sponsor

Eli Lilly and Company

1,341 total trials

What the Registry Record Tells You About NCT01266590

The ClinicalTrials.gov registry entry for NCT01266590 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 30 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 377-participant average among 282 other Major Depressive Disorder trials with a reported enrollment target (92% lower). The listed sponsor is Eli Lilly and Company, which has 1,341 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Major Depressive Disorder appearing as the primary indexed condition, and to 2 interventions - of which Digoxin is the first listed.

NCT01266590 reports 1 study location spanning 1 distinct geographic area - top geographies include Florida.

Frequently Asked Questions

What is clinical trial NCT01266590 about?

NCT01266590 is a clinical study titled "A Study of LY2216684 and Digoxin in Healthy Subjects". The purpose of this study is to determine how much digoxin gets into the blood stream and how long it takes the body to get rid of it when given with LY2216684. Information about any side effects that may occur will also be collected.

What is the current status of trial NCT01266590?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 30 participants. The study started on 2010-12. Estimated completion is 2011-02.

What conditions does trial NCT01266590 study?

This clinical trial studies the following conditions: Major Depressive Disorder.

What interventions are being tested in trial NCT01266590?

The interventions under investigation include: Digoxin (DRUG), LY2216684 (DRUG).

Who is sponsoring clinical trial NCT01266590?

This trial is sponsored by Eli Lilly and Company, which has 1,341 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01266590 being conducted?

This trial has 1 study location across Florida. 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.