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ABSTRACT: Background and aim
This study aimed to determine the efficacy and safety of vedolizumab treatment with or without concomitant immunomodulator use in Japanese patients with moderate-to-severe ulcerative colitis.Methods
Among enrolled patients in a phase 3 study conducted in Japan (clinicaltrials.gov, NCT02039505), data from patients allocated to 300-mg intravenous vedolizumab for induction and maintenance phases were used for this exploratory analysis. Efficacy endpoints were clinical response, clinical remission, and mucosal healing at week 10 and clinical remission and mucosal healing at week 60, and disease worsening and treatment failure during the maintenance phase.Results
At week 10, the differences in clinical response, clinical remission, and mucosal healing
SUBMITTER: Naganuma M
PROVIDER: S-EPMC9293068 | biostudies-literature | 2022 Jan
REPOSITORIES: biostudies-literature