Last updated on August 2019

Study to Compare Oral PF-06651600 PF-06700841 and Placebo in Subjects With Moderate to Severe Ulcerative Colitis


Brief description of study

The purpose of this study is to determine whether PF-06651600 and PF-06700841 are effective in treatment of moderate to severe ulcerative colitis.

Clinical Study Identifier: NCT02958865

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Dothan Surgery Center

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Brighton Surgical Center

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CroNOLA, LLC

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Brigham and Women's Hospital

Chestnut Hill, MA United States
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UMass Memorial Medical Center

Worcester, MA United States
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Concorde medical Group, PLLC

New York, NY United States
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New York, NY United States
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NYU Langone Medical Center

New York, NY United States
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New York, NY United States
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UNC Hospitals, Dept of Pharmacy

Chapel Hill, NC United States
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UNC Hospitals

Chapel Hill, NC United States
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Gastro One

Germantown, TN United States
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Gulf Coast Research Group

Houston, TX United States
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Sagact, Pllc.

San Antonio, TX United States
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Sagact, Pllc

San Antonio, TX United States
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DM Clinical Research

Tomball, TX United States
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Fairfax, VA United States
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Richmond, VA United States
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University of Washington

Seattle, WA United States
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MHAT Blagoevgrad AD

Blagoevgrad, Bulgaria
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Dobrich, Bulgaria
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Medialpharma s.r.o.

Hradec Kralove, Czechia
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Slany, Czechia
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Ustavni lekarna

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Dachau, Germany
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Eugastro GmbH

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Seoul, Korea, Republic of
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Kielce, Poland
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L'Hospitalet de Llobregat, Spain
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Novosibirsk, Russian Federation
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Dallas, TX United States
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Lynchburg, VA United States
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