Study Of The PF-04958242 Blood Concentrations Of A Capsule Formulation Of PF-04958242 Compared To A Solution Formulation
NCT ID: NCT01646840
Last Updated: 2019-11-21
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
2012-07-31
2012-09-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
CROSSOVER
BASIC_SCIENCE
NONE
Study Groups
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PF-04958242 capsule
PF-04958242 capsule
Single dose of PF-04958242 0.35 mg oral capsule
PF-04958242 oral solution
PF-04958242 oral solution
Single dose of PF-04958242 0.35 mg oral solution
Interventions
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PF-04958242 capsule
Single dose of PF-04958242 0.35 mg oral capsule
PF-04958242 oral solution
Single dose of PF-04958242 0.35 mg oral solution
Eligibility Criteria
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Inclusion Criteria
* Body Mass Index (BMI) of 17.5 to 30.5 kg/m2; and a total body weight \>50 kg (110 lbs).
Exclusion Criteria
* Any condition possibly affecting drug absorption (eg, gastrectomy).
18 Years
55 Years
ALL
Yes
Sponsors
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Biogen
INDUSTRY
Responsible Party
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Principal Investigators
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Medical Director
Role: STUDY_DIRECTOR
Biogen
Locations
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Pfizer Investigational Site
New Haven, Connecticut, United States
Countries
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Related Links
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Other Identifiers
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B1701010
Identifier Type: -
Identifier Source: org_study_id
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