A Phase 3, Randomized, Double-Blind, Placebo-Controlled, 12-Week Study To Assess The Efficacy And Safety Of Etrasimod In Subjects With Moderately To Severely Active Ulcerative C
Principal Investigator(s)
          Email for information
              Funded by
              Geneva
          Research Start Date
              Status
              Active
          The primary objective of this study is to assess the efficacy of Etrasimod when administered for twelve (12) weeks on clinical remission in subjects with moderately to severely Active Ulcerative Colitis (UC).
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