Overview

Study of E6007 in Japanese Patients With Moderate Active Ulcerative Colitis

Status:
Completed
Trial end date:
2019-08-16
Target enrollment:
Participant gender:
Summary
This is a randomized, double-blind, placebo-controlled, multi-center study to evaluate the efficacy and safety of E6007 once daily for 8 weeks in Japanese participants with moderate active ulcerative colitis. Participants will be stratified by prior therapeutic treatment and Mayo score at Baseline, and will be randomized 1:1:1 to receive E6007 30 milligrams (mg), E6007 60 mg or placebo.
Phase:
Phase 2
Details
Lead Sponsor:
EA Pharma Co., Ltd.