Absorption, Distribution, Metabolism And Excretion Study For GSK221149A

NCT ID: NCT00457925

Last Updated: 2012-03-19

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

Total Enrollment

6 participants

Study Classification

INTERVENTIONAL

Study Start Date

2006-10-31

Brief Summary

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This is a phase one study investigating the absorption, distribution, metabolism and excretion of GSK221149A in six healthy women of non-child bearing potential.

Detailed Description

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Conditions

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Obstetric Labour, Premature Premature Labor

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Interventions

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GSK221149A

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Healthy adult, non-smoking females
* Aged between 30 - 55 years old, and BMI of between 19 and 32
* Not of child-bearing potential

Exclusion Criteria

* No clinically significant findings on clinical examination, medical examination and blood tests.
* Radiation exposure over previous 3 years is greater than 10mSv
* History of bleeding or gastric problems
Minimum Eligible Age

30 Years

Maximum Eligible Age

55 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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GlaxoSmithKline

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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GSK Clinical Trials

Role: STUDY_DIRECTOR

GlaxoSmithKline

Locations

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GSK Investigational Site

Madison, Wisconsin, United States

Site Status

Countries

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United States

Other Identifiers

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OTA105101

Identifier Type: -

Identifier Source: org_study_id

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