To Investigate The Safety, Toleration And Pharmacokinetics Of Single Oral Doses Of PF-04531083 In Healthy Male Subjects

NCT ID: NCT00992316

Last Updated: 2009-12-17

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

Total Enrollment

80 participants

Study Classification

OBSERVATIONAL

Study Start Date

2009-08-31

Study Completion Date

2009-12-31

Brief Summary

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The purpose of the study is to investigate the safety, toleration and pharmacokinetics of single oral doses of PF-04531083 in healthy male subjects.

Detailed Description

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Conditions

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Pain

Keywords

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Inflammatory pain

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Pf-04531083

To Investigate The Safety, Toleration And Pharmacokinetics Of Single Oral Doses Of PF-04531083 In Healthy Male Subjects

PF-04531083

Intervention Type DRUG

solution. doses to be selected based upon safety/tolerability/PK at preceeding dose

Interventions

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PF-04531083

solution. doses to be selected based upon safety/tolerability/PK at preceeding dose

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* young
* healthy
* male

Exclusion Criteria

* elderly
* unhealthy
* female
Minimum Eligible Age

21 Years

Maximum Eligible Age

55 Years

Eligible Sex

MALE

Accepts Healthy Volunteers

Yes

Sponsors

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Pfizer

INDUSTRY

Sponsor Role lead

Responsible Party

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Pfizer, Inc.

Principal Investigators

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Pfizer CT.gov Call Center

Role: STUDY_DIRECTOR

Pfizer

Locations

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Pfizer Investigational Site

Brussels, , Belgium

Site Status

Countries

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Belgium

Related Links

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Other Identifiers

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B1351001

Identifier Type: -

Identifier Source: org_study_id