A Study of the Effect of INCB013739 on Cortisone Reducing Enzyme Activity in Obese People Predisposed to Diabetes

NCT ID: NCT00398619

Last Updated: 2012-01-23

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE1

Study Classification

INTERVENTIONAL

Study Start Date

2006-11-30

Study Completion Date

2007-03-31

Brief Summary

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The purpose of this study is to determine whether the investigational drug INCB013739 has an effect on systemic and adipose tissue 11-HSD1 activity in obese, insulin resistant subjects.

Detailed Description

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"Proprietary Information: Exploratory (Non-Confirmatory) Trial".

Conditions

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Insulin Resistance Obesity

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Interventions

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INCB13739

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Male and female subjects between 18 years and 65 years of age.
* BMI between 30 and 42 kg/m2, inclusive.
* FPG \<126 mg/dL

Exclusion Criteria

* Meet criteria for diagnosis of diabetes mellitus at the screening evaluation, female subjects with a history of gestational diabetes are permitted.
* Are receiving oral antidiabetic agents within the 3 months prior to screening.
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Incyte Corporation

INDUSTRY

Sponsor Role lead

Principal Investigators

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William V Williams, MD

Role: STUDY_DIRECTOR

Incyte Corporation

Locations

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Beverly Hills, California, United States

Site Status

Chula Vista, California, United States

Site Status

Countries

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United States

Other Identifiers

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INCB13739-103

Identifier Type: -

Identifier Source: org_study_id

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