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Strzyzów, Poland

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  • Dose-finding Study of SAR443122 in Adult Participants With Ulcerative Colitis

    Total study duration per participant will be up to 58 weeks, including a screening period of up to 4 weeks, a treatment period up to 52 weeks and a post-treatment follow-up period of 2 weeks.

    Phase

    2

    Span

    212 weeks

    Sponsor

    Sanofi

    Wloclawek

    Recruiting

  • A Study to Test Whether BI 3032950 Helps People With Ulcerative Colitis

    Phase

    2

    Span

    183 weeks

    Sponsor

    Boehringer Ingelheim

    Wloclawek

    Recruiting

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