The Effects of LY2409021 on the Liver

NCT ID: NCT01588366

Last Updated: 2019-03-07

Study Results

Results available

Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.

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Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE1

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2012-04-30

Study Completion Date

2013-09-30

Brief Summary

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This is a study that involves multiple doses of study drug (60 mg of LY2409021, 15 mg of LY2409021 or placebo) taken as capsules by mouth on a daily basis for 28 days. This study will image the liver using magnetic resonance imaging (MRI) and magnetic resonance spectroscopy (MRS) in healthy participants and in participants with type 2 diabetes mellitus, when they take LY2409021 to see if liver changes happen at the same time as changes in blood tests. This study is approximately 11 weeks long, not including screening. A screening appointment is required within 28 days prior to the start of the study.

Detailed Description

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Conditions

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Diabetes Mellitus, Type 2

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

BASIC_SCIENCE

Blinding Strategy

SINGLE

Participants

Study Groups

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Placebo

Part A and B - Up to 4 capsules of placebo administered orally once a day for 28 days.

Group Type PLACEBO_COMPARATOR

Placebo

Intervention Type DRUG

Administered orally

15 mg LY2409021

Part B - 1 capsule of 15 mg LY2409021 orally once a day for 28 days. (Arm added in September, 2012, per protocol amendment.)

Group Type EXPERIMENTAL

LY2409021

Intervention Type DRUG

Administered orally

60 mg LY2409021

Part A - 4 capsules of 15 mg LY2409021 administered orally once a day for 28 days.

Group Type EXPERIMENTAL

LY2409021

Intervention Type DRUG

Administered orally

Interventions

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Placebo

Administered orally

Intervention Type DRUG

LY2409021

Administered orally

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

For all participants:

* Must be a male, or a female who cannot become pregnant, and who is either a healthy participant, or who has type 2 diabetes
* Must have a body mass index (BMI) of 18.5 to 29.9 kilograms per square meter (kg/m\^2) if a healthy participant, or a BMI of 18.5 to 35.0 kg/m\^2 if diabetic

For participants with type 2 diabetes mellitus (T2DM):

\- On diet and exercise treatment, or taking metformin

Exclusion Criteria

For all participants:

* Have signs or symptoms of liver disease
* Are infected with hepatitis B or hepatitis C
* Have donated more than 450 mL of blood in the last 3 months or if have donated any blood in the last month
* Smoke more than 10 cigarettes per day or are not willing to abstain from smoking while at the clinic
* Have had surgery with metallic clips, staples or stents, or have had a cardiac pacemaker (or other surgical implants) inserted in any part of the body, or have fear of enclosed spaces or have symptoms that prevent them from being sent for an magnetic resonance imaging (MRI) scan

For participants with T2DM:

\- Are using insulin
Minimum Eligible Age

21 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Eli Lilly and Company

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Call 1-877-CTLILLY (1-877-285-4559) or 1-317-615-4559 Mon - Fri 9 AM - 5 PM Eastern time (UTC/GMT - 5 hours, EST)

Role: STUDY_DIRECTOR

Eli Lilly and Company

Locations

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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.

Singapore, , Singapore

Site Status

Countries

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Singapore

Other Identifiers

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I1R-FW-GLBK

Identifier Type: OTHER

Identifier Source: secondary_id

13107

Identifier Type: -

Identifier Source: org_study_id

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