Last updated on April 2018

Study Of PF-06817024 In Healthy Subjects In Patients With Chronic Rhinosinusitis With Nasal Polyps And in Patients With Atopic Dermatitis


Brief description of study

The purpose of this study is to evaluate safety, tolerability, pharmacokinetics, and pharmacodynamics of PF-06817024 in healthy volunteers, in participants with chronic rhinosinusitis, with nasal polyps and in participants with moderate-to-severe Atopic Dermatitis

Detailed Study Description

The purpose of the study for Part 1 is to evaluate the safety and tolerability of PF-06817024 in healthy subjects.

The purpose of the study for Part 2 is to evaluate the safety and tolerability of PF-06817024 in patients with chronic rhinosinusitis with nasal polyps.

The purpose of the study for Part 3 is to evaluate the safety and tolerability of PF-06817024 in patients with moderate-to-severe Atopic Dermatitis

Clinical Study Identifier: NCT02743871

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New Haven Clinical Research Unit
New Haven, CT United States
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Dermatology Physicians of Connecticut
Shelton, CT United States
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Clinical Research Institute, Inc.
Minneapolis, MN United States
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Ear, Nose & Throat Specialty Care of Minnesota, P.A.
Minneapolis, MN United States
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Prism Research, LLC
Saint Paul, MN United States
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Forward Clinical Trials, Inc.
Tampa, FL United States
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Academic Dermatology
Edina, MN United States
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Hassman Research Institute
Berlin, NJ United States
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Vital Prospects Clinical Research Institute, PC
Tulsa, OK United States
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Virginia Clinical Research, Inc.
Norfolk, VA United States
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Dawes Fretzin Clinical Research Group, LLC
Indianapolis, IN United States
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Dawes Fretzin Dermatology Group, LLC
Indianapolis, IN United States
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The Indiana Clinical Trials Center
Plainfield, IN United States
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Carolina Phase 1 Research, LLC
Raleigh, NC United States
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