Last updated on August 2020

A Study to Assess the Efficacy and Safety of Risankizumab in Participants With Ulcerative Colitis Who Responded to Induction Treatment in M16-067 or M16-065


Brief description of study

The purpose of this study is to evaluate safety and efficacy of risankizumab in participants with ulcerative colitis (UC) in participants who responded to induction treatment with risankizumab in a prior AbbVie study of risankizumab in UC.

This study consists of three sub-studies: Substudy 1 is a 52-week, randomized, double-blind, placebo-controlled maintenance study; Substudy 2 is 52-week, randomized, exploratory maintenance study; and Substudy 3 is an open-label long-term extension study for participants who completed Substudy 1 or 2, or participants who responded to induction treatment in Study M16-067 with no final endoscopy due to the Covid-19 pandemic.

Clinical Study Identifier: NCT03398135

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Ucsd /Id# 160430

La Jolla, CA United States
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Advanced Research Institute /ID# 161945

New Port Richey, FL United States
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Indiana University /ID# 167250

Indianapolis, IN United States
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Delricht Research /ID# 206817

New Orleans, LA United States
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Gastro One /ID# 160373

Germantown, TN United States
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Sagact Pllc /Id# 168774

San Antonio, TX United States
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Cemic /Id# 167805

Buenos Aires, Argentina
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Sanatorio 9 de Julio S.A. /ID# 167803

San Miguel de Tucuman, Argentina
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UZ Brussels /ID# 164175

Jette, Brussels, Belgium
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PMI Euromedservice /ID# 204918

Pushkin, Russian Federation
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City Clinical Hospital #40 /ID# 204927

St. Petersburg, Russian Federation
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Dr JP Wright /ID# 171142

Cape Town, South Africa
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Cemic /Id# 167805

Buenos Aires, Argentina
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Recruitment Status: Open


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