Last updated on October 2017

Study To Evaluate The Efficacy And Safety Profile Of PF-06651600 And PF-06700841 In Subjects With Alopecia Areata


Brief description of study

This is a Phase 2a, randomized, double blind, parallel group, multicenter study with an extension period. The study will have a maximum duration of approximately 85 weeks. This includes an up to 5 weeks screening period, a 24 week treatment period, a 4 week drug holiday, an up to 12 month extension period, and a 4 week follow up period. The study will enroll a total of approximately 132 subjects. The study will be conducted at approximately 30 to 40 sites.

Clinical Study Identifier: NCT02974868

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University of Alabama at Birmingham
Birmingham, AL United States
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Southern California Dermatology, Inc.
Santa Ana, CA United States
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Clinical Science Institute
Santa Monica, CA United States
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University of Colorado Hospital Clinical and Translational Research Center, Inpatient Unit
Aurora, CO United States
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University of Colorado Hospital Clinical and Translational Research Center, Outpatient Clinic
Aurora, CO United States
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University of Colorado Hospital, Anschutz Cancer Pavilion
Aurora, CO United States
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Yale New Haven Hospital - Hospital Research Unit
New Haven, CT United States
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Yale New Haven Hospital - Radiology
New Haven, CT United States
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Yale School of Medicine
New Haven, CT United States
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Investigational Drug Services
New Haven, CT United States
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Church Street Research Unit
New Haven, CT United States
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Park Avenue Dermatology Administrative Annex
Orange Park, FL United States
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Park Avenue Dermatology
Orange Park, FL United States
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Olympian Clinical Research
Tampa, FL United States
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Rose Radiology
Tampa, FL United States
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Forward Clinical Trials, Inc
Tampa, FL United States
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MedaPhase Inc.
Newnan, GA United States
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NorthShore University HealthSystem Dermatology Clinical Trials Unit
Skokie, IL 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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Tufts Medical Center
Boston, MA United States
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Massachusetts General Hospital Clinical Unit for Research Trials in Skin (CURTIS)
Boston, MA United States
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Icahn School of Medicine at Mount Sinai
New York, NY United States
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Mount Sinai Department of Otolaryngology
New York, NY United States
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Rockefeller University Hospital
New York, NY United States
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Investigational Drug Service
Rochester, NY United States
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University of Rochester Medical Center
Rochester, NY United States
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Vital Prospects Clinical Research Institute, P.C.
Tulsa, OK United States
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Health Concepts
Rapid City, SD United States
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University of Utah MidValley Dermatology
Murray, UT United States
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University of Utah Medical Center
Salt Lake City, UT United States
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Virginia Clinical Research, Inc.
Norfolk, VA United States
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St George Dermatology and Skin Cancer Centre
Kogarah, Australia
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The Skin Centre
Benowa, Australia
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Veracity Clinical Research
Woolloongabba, Australia
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Skin & Cancer Foundation Inc.
Carlton, Australia
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Sinclair Dermatology
East Melbourne, Australia
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Wiseman Dermatology Research Inc.
Winnipeg, MB Canada
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Lynderm Research Inc.
Markham, ON Canada
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Research by ICLS
Oakville, ON Canada
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SKiN Centre for Dermatology
Peterborough, ON Canada
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The Centre for Dermatology
Richmond Hill, ON Canada
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York Dermatology Center
Richmond Hill, ON Canada
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