Phase III Study of ASP0456 - A Double-blind, Placebo-controlled, Parallel-group, Comparative Study and Long-term Study in Patients With Irritable Bowel Syndrome With Constipation (IBS-C)
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 500
- 试验地点
- 61
- 主要终点
- Responder rate of Global assessment of relief of IBS symptoms during 12 weeks.
研究概览
简要总结
The objective of this study is to evaluate the efficacy and safety of ASP0456 in patients with constipation predominant irritable bowel syndrome (IBS-C).
详细描述
<Period I (double-blind period)> A multicenter, collaborative, double-blind, parallel comparative study is conducted using IBS-C patients as subjects to verify efficacy of ASP0456 and examine the safety. After the 2-week bowel habit observation period, subjects satisfying the primary enrollment criteria are randomly allocated to either ASP0456 group or placebo group, and orally administered the drug or placebo once daily before breakfast for 12 weeks.
<Period II (non-blind period)> A multicenter, collaborative, non-blind, non-controlled study is conducted to examine safety and efficacy of ASP0456 in long-term administration in IBS-C patients. After Period I, subjects satisfying the transfer criteria are orally administered ASP0456 once daily before breakfast for 40 weeks.
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
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 20 Years 至 79 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients who had abdominal pain or discomfort repeatedly for at least 3 days per month during the 3 months before screening examination associated with at least 2 out of the following 3 conditions: (1) Improvement with defecation; (2) Onset associated with a change in frequency of stool; and (3) Onset associated with a change in form (appearance) of stool, and had the above symptom (IBS symptom) 6 months or more before the screening examination period
- •Patients with ≥ 25% of stools hard or lumpy (with each bowel movement occurring without antidiarrheal, laxative, suppository or enema) and <25% of them loose (mushy) or watery during the 3 months before the screening examination
- •Patients who had pancolonoscopy or contrast enema (or sigmoidoscopy) after the onset of IBS symptom and had no organic changes
排除标准
- •Patient with history of surgical resection of stomach, gallbladder, small intestine, or large intestine (excluding resection of appendicitis and benign polyp)
- •Patient with history or current affection of inflammatory bowel disease (Crohn's disease or ulcerative colitis)
- •Patient with history or current affection of ischemic colitis
- •Patient currently affected by infectious enteritis
- •Patient currently affected by hyperthyroidism or hypothyroidism
- •Patient currently affected by active peptic ulcer
- •In the case of a female patient, the one currently affected by endometriosis or uterine adenomyosis
- •Patient with high depression or anxiety considered to influence drug evaluation
- •Patient with history of abuse of drug or alcohol within a year before consent acquisition, or with current abuse
- •Patient who used or underwent or will use or undergo drug/therapy/test prohibited to combine 3 days before the start of bowel habit observation period (Day -17) or thereafter
- •Patient with history or current affection of malignant tumor
- •Patient currently affected by serious cardiovascular disease, respiratory disease, kidney disease, hepatic disease, gastrointestinal disease (excluding IBS), hemorrhagic disease, or neural/mental disease
- •Patient with history of drug allergy
研究组 & 干预措施
ASP0456 (Period I)
Up to 12 weeks
干预措施: linaclotide (Drug)
Placebo (Period I)
Up to 12 weeks
干预措施: Placebo (Drug)
ASP0456 (Period II)
From 12 weeks to 52 weeks
干预措施: linaclotide (Drug)
结局指标
主要结局
Responder rate of Global assessment of relief of IBS symptoms during 12 weeks.
时间窗: During 12 weeks
The responder of the evaluation items during the 12 weeks shall be the subject satisfying weekly responder of the evaluation items for over 6 weeks of the 12 weeks.
Responder rate of CSBM during 12 weeks
时间窗: During 12 weeks
CSBM: Complete Spontaneous Bowel Movement. The responder of the evaluation items during the 12 weeks shall be the subject satisfying weekly responder of the evaluation items for over 6 weeks of the 12 weeks.
次要结局
- Responder rate of SBM during 12 weeks(During 12 weeks)
- Responder rate of Abnormal bowel habits improvement during 12 weeks(During 12 weeks)
- Responder rate of Abdominal pain/discomfort relief during 12 weeks(During 12 weeks)
- Weekly responder rate of Global assessment of relief of IBS symptoms(Up to 52 weeks)
- Weekly responder rate of CSBM(Up to 52 weeks)
- Weekly responder rate of SBM(Up to 52 weeks)
- Weekly responder rate of Abnormal bowel habits improvement(Up to 52 weeks)
- Weekly responder rate of Abdominal pain/discomfort relief(Up to 52 weeks)
- Changes in weekly average of SBM frequency, CSBM frequency, stool form scores, abdominal pain/discomfort severity, abdominal bloating severity, and straining severity.(From baseline to every week until 52 weeks)
- Changes in IBS-QOL-J scores (entire scores or scores on the sub-scales)(Weeks 0, 4, 8, 12, 16, 20, 24, 28, 40, 52)
- Percentage of subjects with SBM within 24 hours after start of the initial administration(Up to 24 hours)
- Percentage of subjects with CSBM within 24 hours after start of the initial administration(Up to 24 hours)
- Safety assessed by development of incidence of adverse events, vital signs, and clinical laboratory tests(Up to 52 weeks)