A Study to Compare the Safety and Drug Levels in Blood When Using Various Forms of GSK189075 Given to Healthy Subjects - Full Text View

Sponsored by:	GlaxoSmithKline
Information provided by:	GlaxoSmithKline
ClinicalTrials.gov Identifier:	NCT00559884

Purpose

The purpose of this research study is to look at concentrations of GSK189075 in blood when different long and short acting forms of the drug are taken by mouth. The results will help to decide whether a long-acting form of GSK189075 can be made. The effects of the drug on the body and safety will also be studied.

Condition	Intervention	Phase
Type 2 Diabetes Mellitus	Drug: GSK189075 (Modified and immediate release formulations)	Phase I

MedlinePlus related topics: Diabetes

U.S. FDA Resources

Study Type:	Interventional
Study Design:	Treatment, Randomized, Open Label, Crossover Assignment, Bio-availability Study
Official Title:	An Open-Label, Randomized, Single Dose, Crossover Study to Assess the Pharmacokinetics, Pharmacodynamics, Safety, and Tolerability of Modified Release Formulations of GSK189075 in Healthy Volunteers

Further study details as provided by GlaxoSmithKline:

Primary Outcome Measures:

Blood samples: [ Time Frame: collected over 24-hour period after each different form of GSK189075 given to measure amount of drug in blood ]
Urine: [ Time Frame: collected over 24-hour period after dosing with each form to measure amount of urine produced & amount of sugar in urine ]

Secondary Outcome Measures:

Adverse events: [ Time Frame: all visits after Day -1 ]
blood pressure & heart rate: [ Time Frame: screening,Day -1 - Day 1,follow-up visit ]
ECGs: [ Time Frame: screening,pre-dose, Day 1 ]
lab tests: [ Time Frame: screening, Day -1 - Day 1,follow-up ]

Enrollment:	36
Study Start Date:	November 2007

Eligibility

Ages Eligible for Study:	18 Years to 55 Years
Genders Eligible for Study:	Both
Accepts Healthy Volunteers:	Yes

Criteria

Inclusion Criteria:

Are a healthy, non-smoking adult, 18 to 55 years old.
Are not overly thin or overly heavy for your height.
Are a female who is unable to have children, or is willing to use birth control throughout the study.
Are willing and able to follow all study-related instructions provided by the site staff. - Are willing to provide signed consent.

Exclusion Criteria:

Are a pregnant or a nursing female.
Have a past or current disease such as heart, liver, kidney, blood, brain, or other disease.
Have had certain infections within 4 weeks before the expected the first dose of study drug.
Have HIV or hepatitis, or have alcohol in your system at the screening visit.
Have a history of alcohol abuse.
Have been in another research study in the last month or have taken certain medications in the 2 weeks before study drug would be taken.
Have laboratory tests that are outside the normal range.

Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00559884

Locations

United States, Ohio
GSK Investigational Site
Columbus, Ohio, United States, 43212

Sponsors and Collaborators

GlaxoSmithKline

Investigators

Study Director:

GSK Clinical Trials, MD, PhD

GlaxoSmithKline

More Information

Responsible Party:	GSK ( Study Director )
Study ID Numbers:	KGW111057
Study First Received:	November 14, 2007
Last Updated:	October 9, 2008
ClinicalTrials.gov Identifier:	NCT00559884
Health Authority:	United States: Food and Drug Administration

Keywords provided by GlaxoSmithKline:

healthy male and females,
pharmacokinetics,
pharmacodynamics

Study placed in the following topic categories:

Metabolic Diseases
Diabetes Mellitus, Type 2
Diabetes Mellitus
Endocrine System Diseases

Endocrinopathy
Healthy
Metabolic disorder
Glucose Metabolism Disorders

ClinicalTrials.gov processed this record on January 16, 2009