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临床试验/NCT03707730
NCT03707730已完成2 期

A Randomized, Double-Blind, Placebo Controlled, Crossover Trial to Evaluate Safety and Efficacy of AGY in Persons With Celiac Disease Age > 10 Years

Igy Inc.4 个研究点 分布在 1 个国家目标入组 161 人开始时间: 2019年10月29日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
161
试验地点
4
主要终点
symptoms

研究概览

简要总结

To assess the efficacy and safety of AGY vs placebo when administered to individuals age 10 to 65 years with medically proven CD and on a gluten free diet

详细描述

We propose to conduct a randomized double-blind, placebo-controlled crossover trial in 149 individuals with celiac disease proven by biopsy (or other medically documented confirmation of CD, e.g. TTG counts > 10 times the upper limit of normal on two occasions) at least 12 months before study entry, and who are following a gluten-free diet but continue to have recurrent symptoms.

AGY is designed to neutralize the hidden gliadin in food, thus preventing gliadin absorption and gliadin induced pathogenesis. The study will test whether AGY is safe and effective in the study population, versus placebo.

Primary Objective: The primary objective will be to evaluate the effect of AGY on celiac symptoms using the daily Celiac Symptom Index (CSI).

Secondary objectives: Secondary objectives will be to evaluate product safety and the effect of AGY on quality of life, autoantibodies, and gut permeability.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

盲法说明

placebo controlled

入排标准

年龄范围
10 Years 至 65 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • history of CD
  • experience periodic celiac related symptoms
  • following a gluten free diet for at least 12 months

排除标准

  • severe complications of CD or chronic active GI disease
  • type 1 diabetic
  • pregnant or breast feeding
  • daily ASA/NSAID use
  • any condition that in the opinion of the investigator, would preclude safe participation

结局指标

主要结局

symptoms

时间窗: 14 weeks

celiac related symptoms

次要结局

未报告次要终点

研究者

发起方
Igy Inc.
申办方类型
Industry
责任方
Sponsor

研究点 (4)

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