A Study To Investigate The Absorption, Metabolism And Excretion Of [14C] PD 0200390 In Six Healthy Male Volunteers

NCT ID: NCT00722306

Last Updated: 2011-02-04

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

2008-05-31

Study Completion Date

2008-05-31

Brief Summary

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To determine the mass balance of PD 0200390

Detailed Description

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Conditions

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Insomnia

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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A425

A425 Treated

Group Type EXPERIMENTAL

PD 0200390

Intervention Type DRUG

Extemporaneous solution of C14 Labelled PD 0200390 60 mg single dose

Interventions

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PD 0200390

Extemporaneous solution of C14 Labelled PD 0200390 60 mg single dose

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Healthy

Exclusion Criteria

* unhealthy, or concomitant meds
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

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

New Haven, Connecticut, United States

Site Status

Countries

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United States

Related Links

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Other Identifiers

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A4251072

Identifier Type: -

Identifier Source: org_study_id

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