A Multicenter Randomized Double-Blind Placebo-Controlled 52-Week Maintenance and an Open-Label Extension Study of the Efficacy and Safety of Risankizumab in Subjects with Ulcerative Colitis Who Responded to Induction Treatment in M16-067 or M16-065

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Updated on 19 February 2024

Summary

The study will enroll subjects who have completed Study M16-067 or Study M16-065 and have achieved clinical response, defined as decrease from Baseline of induction study of Adapted Mayo score greater than or equal to 2 points and greater than or equal to 30%, PLUS a decrease in rectal bleeding sub-score (RBS) greater than or equal to 1 or an absolute RBS less than or equal to 1 .

Details
Condition ulcerative colitis
Age 99years or below
Clinical Study IdentifierTBD
Last Modified on19 February 2024

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