Last updated on March 2020

A Multicenter Randomized Double-Blind Placebo Controlled Induction Study to Evaluate the Efficacy and Safety of Risankizumab in Subjects With Moderately to Severely Active Ulcerative Colitis Who Have Failed Prior Biologic Therapy

Brief description of study

The objectives of Sub-Study 1 are to evaluate the efficacy, safety, and pharmacokinetics of risankizumab as induction treatment in subjects with moderately to severely active ulcerative colitis (UC), and to identify the appropriate induction dose of risankizumab for further evaluation in Sub-Study 2.

The objective of Sub-Study 2 is to evaluate the efficacy and safety of risankizumab compared to placebo in inducing clinical remission in subjects with moderately to severely active UC.

Clinical Study Identifier: NCT03398148

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Ucsd /Id# 160452

La Jolla, CA United States
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Advanced Research Institute /ID# 161938

New Port Richey, FL United States
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Indiana University /ID# 167252

Indianapolis, IN United States
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Delricht Research /ID# 206815

New Orleans, LA United States
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Gastro One /ID# 160418

Germantown, TN United States
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Sagact Pllc /Id# 168776

San Antonio, TX United States
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Cemic /Id# 167782

Buenos Aires, Argentina
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Sanatorio 9 de Julio S.A. /ID# 167780

San Miguel de Tucuman, Argentina
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UZ Brussels /ID# 164176

Jette, Brussels, Belgium
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PMI Euromedservice /ID# 204892

Pushkin, Russian Federation
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City Clinical Hospital #40 /ID# 203370

St. Petersburg, Russian Federation
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Dr JP Wright /ID# 171138

Cape Town, South Africa
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