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NCT01301092 · ClinicalTrials.gov registry record · Phase 1

A Study to Compare the Concentrations of LY2189265 After Different Methods of Administration to Healthy Volunteers.

A Phase 1 study, sponsored by Eli Lilly and Company.

Completed
Registry status
Phase 1
Development phase
30
Enrollment target

NCT01301092 is a Phase 1 study that has completed, run by Eli Lilly and Company. The registered enrollment target is 30 participants.

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The verdict

NCT01301092, a Phase 1 study, has completed, sponsored by Eli Lilly and Company.

COMPLETED
Registry status
Phase 1
Development phase
30 participants
Enrollment target

Study Summary

LY2189265 is an investigational drug being developed for the treatment of type 2 diabetes mellitus. This study will compare the concentrations of LY2189265 using different methods of administration: subcutaneous (or SC- an injection just under the skin), intravenous (or IV - into a vein in the arm) and intramuscular (IM - into the muscle of the left thigh). The purpose of this study is to look at how much of the drug gets into the blood stream and how long it takes the body to get rid of it when given by the methods above. The study is divided into three parts, Part A, B and C. Volunteers will only be able to participate in one part. All Participants in Part A will receive a single IV dose of up to 0.1 milligram (mg). Participants in Part B will be given drug twice by IV and an SC injection (1.5 mg). Part B of the study will occur after Part A because the dose of IV drug will depend on the results of Part A. Part B of the study may not occur if the volunteers in Part A do not tolerate the drug. Participants in Part C will also be given drug twice by an SC injection and an IM injection, both doses will be 0.75 mg.

Interventions

  • BIOLOGICAL LY2189265

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2011-02
Est. Completion 2011-08
Phase Phase 1

Sponsor

Eli Lilly and Company

1,341 total trials

What the Registry Record Tells You About NCT01301092

The ClinicalTrials.gov registry entry for NCT01301092 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. The listed sponsor is Eli Lilly and Company, which has 1,341 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which LY2189265 is the first listed.

NCT01301092 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01301092 about?

NCT01301092 is a clinical study titled "A Study to Compare the Concentrations of LY2189265 After Different Methods of Administration to Healthy Volunteers.". LY2189265 is an investigational drug being developed for the treatment of type 2 diabetes mellitus. This study will compare the concentrations of LY2189265 using different methods of administration: subcutaneous (or SC- an injection just under the skin), intravenous (or IV - into a vein in the arm) ...

What is the current status of trial NCT01301092?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 30 participants. The study started on 2011-02. Estimated completion is 2011-08.

What interventions are being tested in trial NCT01301092?

The interventions under investigation include: LY2189265 (BIOLOGICAL).

Who is sponsoring clinical trial NCT01301092?

This trial is sponsored by Eli Lilly and Company, which has 1,341 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.