A Randomized, Double-Blind, Placebo-Controlled Parallel Group Study to Assess the Efficacy and Safety of Induction Therapy With LYC-30937-EC in Subjects With Active Ulcerative Colitis
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- Lycera Corp.
- 入组人数
- 124
- 试验地点
- 3
- 主要终点
- Number of Subjects Who Achieve Clinical Remission at Week 8 Using Modified Mayo Score.
研究概览
简要总结
The purpose of the study is to evaluate the efficacy and safety of LYC-30937-EC given orally once daily in subjects with active ulcerative colitis (UC) defined as a total Mayo score (TMS) of 4-11 inclusive, with an endoscopic score of ≥ 2 and a rectal bleeding score of ≥ 1 at screening.
详细描述
Approximately 120 subjects will be randomized to receive either enteric-coated (EC) LYC-30937-EC 25 mg PO once daily (QD) or matching placebo PO QD for the duration of 8 weeks. Randomization will be stratified based on previous exposure to anti-tumor necrosis factor (TNF) agents such that at least 50% of the randomized subjects will be anti-TNF naïve .
The study will consist of 3 phases:
- screening phase: up to 4 weeks
- double-blind placebo-controlled phase treatment: 8 weeks
- post-treatment follow-up: 2 weeks
Eligible subjects will be randomized at Week 0 (Study Day 1) to either LYC-30937-EC 25 mg or placebo. Screening will occur from Study Days -28 to -1. Randomization and first dosing will occur at Week 0/Study Day 1. Double-blind study visits will occur at Weeks 2, 4, and 8, with the last dose at Week 8/Study Day 57. Subjects will return at Week 10 for a post-treatment safety follow-up visit.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Double (Participant, Investigator)
入排标准
- 年龄范围
- 18 Years 至 75 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Clinical UC diagnosis ≥ 6 months prior to screening with minimum disease extent of ≥ 15cm from anal verge.
- •Active UC defined as a TMS of 4-11 (inclusive) with endoscopic subscore of ≥ 2 and rectal bleeding subscore of ≥ 1 at screening.
- •Females of childbearing potential must have a negative pregnancy test at screening and baseline visits and must agree to use acceptable methods of birth control while in the trial and for 30 days after taking the last dose of study drug.
- •May be currently receiving treatment with oral aminosalicylates (ASA) for ≥ 6 weeks at a stable dose for ≥ 3 weeks prior to the screening screening endoscopy and/or thiopurine at a stable dose ≥ 8 weeks prior to the screening endoscopy and/or prednisone (dose 20 mg daily) or equivalent for ≥ 4 weeks and receiving stable dose for ≥ 2 weeks prior to screening endoscopy
- •able to provide written informed consent and be compliant with study procedures.
排除标准
- •History of Crohn's disease (CD) or indeterminate colitis or the presence or history of fistula consistent with CD.
- •Presence of colon polyps.
- •Severe extensive disease that in the investigators discretion is likely to require colonic surgery during the 8 week double-blind portion of the trial (eg, fulminant colitis, toxic megacolon, bowel perforation, evidence of acute abdomen).
- •History of alcohol or drug abuse within 1 year of randomization.
- •History of cancer including solid tumors and hematological malignancies (except basal cell and in situ squamous cell carcinomas of the skin that have been adequately treated with no recurrence for ≥ 1 year prior to screening.
- •History or currently active primary or secondary immunodeficiency.
- •Clinically relevant hepatic, neurologic, pulmonary, ophthalmological, gastrointestinal, endocrine, psychiatric, or other major systemic disease making implementation of the study difficult or that would put the subject at risk by participating in the study
- •Positive test for Clostridium difficile or positive stool culture for enteric pathogens or presence of ova or parasites at screening.
- •Liver function tests > 1.5 x upper limit of normal (ULN) or direct bilirubin > 1.5 x ULN
- •Hemoglobin < 8.5 g/dl
- •Neutrophils < 1500/mm3
- •White blood cell (WBC) count < 3000/mm3
- •Platelets < 80000 mm3
- •International normalized ratio (INR) > 1.5
- •Treatment with an immunosuppressant agent within 8 weeks of screening.
- •Previous exposure to ≥ 2 approved or investigational biologic agents to treat UC.
- •History of UC treatment with a biologic agent within 12 weeks of screening.
- •Treatment with rectal steroids within 2 weeks of screening.
- •Treatment with an investigational agent within 30 days of screening.
研究组 & 干预措施
LYC-30937-EC 25 mg PO QD
LYC-30937-EC 25 mg by mouth once daily for 8 weeks
干预措施: LYC-30937-EC (Drug)
Placebo PO QD
Matching placebo by mouth once daily for 8 weeks
干预措施: Placebo (Drug)
结局指标
主要结局
Number of Subjects Who Achieve Clinical Remission at Week 8 Using Modified Mayo Score.
时间窗: 8 weeks
The modified Mayo score is a tool designed to measure disease activity for ulcerative colitis. Scoring ranges from 0 to 9 points and consists of 3 subscores (stool frequency, rectal bleeding, endoscopy), each graded 0 to 3 with higher score indicating more severe disease activity. Endoscopy scoring was performed centrally. Clinical remission on the modified Mayo score was defined as a Mayo stool frequency subscore of ≤ 1, Mayo rectal bleeding subscore of 0 and a Mayo endoscopy subscore of ≤ 1.
次要结局
- Number of Subjects Who Achieve Clinical Remission at Week 8 Using the Total Mayo Score.(8 weeks)
- Number of Subjects With a Clinical Response on the Modified Mayo Score at Week 8.(8 weeks)
- Number of Subjects With a Clinical Response on the Total Mayo Score at Week 8.(8 weeks)
- Percent Change From Baseline to Week 8 in Fecal Calprotectin in Subjects With Baseline Fecal Calprotectin ≥ 250 µg/g(Baseline to Week 8)
- Percent Change From Baseline in Total Mayo Score at Week 8.(Baseline to Week 8)