Last updated on July 2019

A Global Study Comparing Risankizumab to Placebo in Adult Participants With Moderate to Severe Hidradenitis Suppurativa


Brief description of study

This study is to evaluate the safety and efficacy of 2 dose levels of risankizumab in adult participants with moderate to severe Hidradenitis Suppurativa (HS). This study includes two treatment periods. In Period A, participants are randomized to receive either risankizumab dose A, dose B, or placebo. In Period B, participants who received risankizumab dose A or placebo during Period A, will receive risankizumab dose B. Participants who received risankizumab dose B in Period A will remain on that dose in Period B.

Clinical Study Identifier: NCT03926169

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Bravis Ziekenhuis /ID# 212536

Bergen op Zoom, Netherlands
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Hamzavi Dermatology /ID# 212318

Fort Gratiot, MI United States
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Hopital Nord /ID# 212564

Saint Priest En Jarez, France
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Recruitment Status: Open


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