A 54-Week, Multicenter, Randomized, Double-blind, Placebo-controlled, Parallel-group Phase 2 Study to Assess the Efficacy and Safety of Brazikumab in Participants with Moderately to Severely Active Ulcerative Colitis (Expedition Lead-in) - Phase 2 Dose-finding UC Study

AstraZeneca AB0 个研究点目标入组 255 人2019年11月7日

概览

暂无简介。

注册库

who.int

开始日期

2019年11月7日

结束日期

待定

最后更新

2年前

研究类型

Interventional clinical trial of medicinal product

性别

All

发起方

•1\.Ability to provide informed consent prior to any study procedures and willing and able to attend all study visits.
•2\.Aged 18 to 80 years of age at the time of signing the informed consent.
•3\.Diagnosis of UC with an onset of symptoms for a minimum of 3 months prior to Screening.
•4\.Evidence of UC extending proximal to the rectum (\= 15 cm of involved colon).
•5\.Moderately to severely active UC as defined by (5a and 5b must be met):
•(a) Stool Frequency and Rectal Bleeding subscores obtained during Screening on an eDiary.
•i. Average daily mMS Stool Frequency subscore \= 1 AND
•ii. Average daily mMS Rectal Bleeding subscore \= 1
•(b) Modified Mayo endoscopic subscore of \= 2 based on a full colonoscopy within 14 days prior to initial IRT randomization.
•6\.Participant had an inadequate response or intolerance to intervention with conventional treatment (oral CS, azathioprine, methotrexate, or 6 mercaptopurine) or prior biological treatment or demonstrated CS dependence for the treatment of UC. For participants who have previously used biological treatment, a participant may have failed up to 3 biologics that include up to 2 different mechanisms of action.

•1\.Participant has UC limited to the rectum (ie, not beyond 15 cm of the anal verge).
•2\.Current diagnosis of fulminant colitis, a diagnosis of CD or indeterminate colitis, presence or history of a fistula consistent with CD, primary sclerosing cholangitis, celiac disease, or untreated bile acid malabsorption. Participants with a history of toxic megacolon within 12 months of Screening are excluded.
•3\.History of subtotal colectomy with ileorectostomy or colectomy with ileoanal pouch, Koch pouch, ileostomy, or other prior colonic resection, or need for surgical intervention for control of UC anticipated within 6 months.
•4\.Participant has received the following treatment:
•(a) Infliximab: within 8 weeks prior to randomization.
•(b) Adalimumab, certolizumab pegol, or golimumab: within 8 weeks prior to randomization.
•(c) Vedolizumab or ustekinumab within 12 weeks of randomization.
•(d) Other prohibited medication, biologic or small molecule treatment within 5 half\-lives prior to randomization.
•(e) Fecal microbiota transplantation: within 8 weeks prior to randomization.
•5\. Removed as part of Amd5