A Study To Compare The Pharmacokinetics Of Different Formulations Of PF-04937319 In Healthy Subjects
NCT ID: NCT01513928
Last Updated: 2012-03-12
Study Results
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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COMPLETED
PHASE1
12 participants
INTERVENTIONAL
2012-01-31
2012-02-29
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
BASIC_SCIENCE
NONE
Interventions
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Pf-04937319
Formulation A) Pf-04937319 50 mg - administered as tablet
Pf-04937319
Formulation B) Pf-04937319 50 mg - administered as capsule
Pf-04937319
Formulation C) Pf-04937319 50 mg - administered as capsule
Eligibility Criteria
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Inclusion Criteria
* Subjects of childbearing potential must agree to use a highly effective method of contraception throughout the study and for at least 28-days after the last dose of treatment.
* Body Mass Index (BMI) of 23 to 33 kg/m2 and a total body weight \>=50 kg (110 lbs).
Exclusion Criteria
* Any condition possibly affecting drug absorption (eg, gastrectomy).
* A positive urine drug screen.
21 Years
55 Years
ALL
Yes
Sponsors
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Pfizer
INDUSTRY
Responsible Party
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Principal Investigators
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Pfizer CT.gov Call Center
Role: STUDY_DIRECTOR
Pfizer
Locations
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Pfizer Investigational Site
Singapore, Singapore, Singapore
Countries
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Related Links
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Other Identifiers
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B1621005
Identifier Type: -
Identifier Source: org_study_id
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