Last updated on March 2019

A Study of the Efficacy and Safety of Upadacitnib (ABT-494) in Subjects With Moderately to Severely Active Crohn's Disease Who Have Inadequately Responded to or Are Intolerant to Conventional Therapies But Have Not Failed Biologic Therapy

Brief description of study

The objective of this study is to evaluate the efficacy and safety of upadacitinib compared to placebo as induction therapy in participants with moderately and severely active Crohn's disease (CD).

Clinical Study Identifier: NCT03345849

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Facey Medical Foundation /ID# 203136

Mission Hills, CA United States
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Ucsd /Id# 164910

San Diego, CA United States
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Delta Waves, Inc. /ID# 164776

Colorado Springs, CO United States
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Borland-Groover Clinic /ID# 203499

Jacksonville, FL United States
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Advanced Research Institute /ID# 164921

New Port Richey, FL United States
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DuPage Medical Group /ID# 205328

Downers Grove, IL United States
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Indiana University /ID# 164909

Indianapolis, IN United States
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Tri-State Gastroenterology /ID# 165496

Crestview Hills, KY United States
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CroNOLA, LLC /ID# 164823

Houma, LA United States
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NY Scientific /ID# 164931

Brooklyn, NY United States
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Gastro One /ID# 164826

Germantown, TN United States
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Sagact Pllc /Id# 169755

San Antonio, TX United States
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Care Access Research /ID# 164794

Salt Lake City, UT United States
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Cemic /Id# 169182

Buenos Aires, Argentina
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Hospital Centenario /Id# 171252

Rosario, Santa FE, Argentina
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Aquiant Research /ID# 205503

New Albany, IN United States
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LLC Novaya Klinika /ID# 206616

Pyatigorsk, Russian Federation
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PMI Euromedservice /ID# 206610

Pushkin, Russian Federation
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Dr JP Wright /ID# 170887

Cape Town, South Africa
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Kingston Hosp NHS Foundation /ID# 200649

Kingston upon Thames, United Kingdom
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Royal Victoria Infirmary, Newc /ID# 169075

Newcastle Upon Tyne, United Kingdom
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Crchum /Id# 170120

Montreal, QC Canada
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Recruitment Status: Open

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