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临床试验/NCT04788797
NCT04788797已完成4 期

Effect of the Endopeptidase AN-PEP on Gluten Exposure in Real Life in Celiac Disease Patients Treated With a Long-term Gluten-free Diet. Exploratory, Interventional, Prospective, Controlled and Double Blind Study

Dr. C. Bonorino Udaondo Gastroenterology Hospital1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2021年3月17日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
40
试验地点
1
主要终点
Weekly concentration of GIP excretion in stool

研究概览

简要总结

The AN-PEP, an Aspergillus niger derived endopeptidase, has been developed aiming to produce a complete luminal detoxification of gluten. If AN-PEP is able to produce a complete luminal digestion of gluten in the context of the real life of celiac disease (CeD) patients is unknown. Hypothetically, AN-PEP effect could be detected by the reduction in the excretion of GIP in stool and urine.

The objective of this study is to establish the effect of the daily administration of AN-PEP compared to placebo on GIP excretion in an interventional, prospective, randomized, comparative, double-blind study in conditions mimicking the real-life of CeD treated patients. The study consists in a four-week GFD stabilization period followed by a four-week study period with patients randomized to receive active AN-PEP or placebo in a blindly manner.

详细描述

Background: The strict gluten-free diet (GFD) is the only accepted treatment for celiac disease (CeD). However, performing a strict diet is still a non solved problem affecting the future of patients. In a real-life study it was recently shown that 89% of treated CeD patients performing a strict diet have contact with dietary gluten at least one week per 4 weeks of testing and averaging 3 weeks per month. Furthermore, 40% of patients excreted gliadin immunogenic peptides (GIP) (surrogated markers of gluten exposure) in the range for immunological activation and intestinal mucosal damage. Endopeptidases to produce a complete intraluminal proteolysis of gluten avoiding antigenic stimulation were produced to avoid damage of continuous gluten exposure. AN-PEP is an Aspergillus niger derived endopeptidase has been produced aiming to luminal detoxification of gluten have been explored for its clinical effect. However, whether AN-PEP is able to completely destroy gluten in the context of the real life of CeD patients is still unknown. Hypothesis: The investigators estimate that AN-PEP is an effective therapy for proteolysis for gluten exposure in the real-life of CeD patients and that the effect could be detected by the reduction in the excretion of GIP in stool and urine based on a clinical research model that we developed. AIMS: to establish the effect of daily administration of AN-PEP compared to placebo in terms of: (1) frequency of GIP excretion in stool and urine episodes in 4 weeks; (2) concentration of GIP excretion for both arms; and (3) differences in proportion of patients excreting GIP above the threshold for mucosal damage (>2 µg/g of GIP in stool or >12 ng/mL in urine). Study design: Interventional, prospective, randomized, comparative, double-blind study. Components: 1- four-week GFD stabilization period; 2-Randomization. 3- four4-week study period: Patients blinded-receive active AN-PEP (GliadinX®) at a dose of 2 capsules/breakfast, lunch and dinner (study arm), or 2 capsules at same time points of placebo (specially designed and prepared for the study) (Placebo arm).

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
17 Years 至 75 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Over 18 years
  • Diagnosis of celiac disease
  • Completion of Gluten-free Diet for at least two years without evidence of voluntary violations.
  • Patients who do not report symptoms of constipation or illnesses or medications (cathartics, antidiarrheals, etc.) that alter the bowel movement rhythm (accepted rhythm: between 2 times / day to 1 every other day) and diuresis (diuretics). Proton-pump inhibitor.
  • Signature of the informed consent

排除标准

  • Patients not interested or unable to collaborate with the questionnaires and collection of fecal matter.
  • Place of residence of the participant more than 4 hours from the hospital, which interferes with the viability of the sample.
  • Complicated CD (refractory CD type II, ulcerative jejunoileitis, lymphoma).
  • Concomitant pathologies that are decompensated or untreated at study entry (type I or II diabetes mellitus; hyperthyroidism; hypothyroidism; kidney failure,).

研究组 & 干预措施

Prolyl Endopeptidase

Active Comparator

Patients blinded-receive active AN-PEP at a dose of 2 capsules/breakfast, lunch and dinner during 8 weeks (study arm)

干预措施: Prolyl Endopeptidase (Drug)

Placebo

Placebo Comparator

Patients blinded-receive 2 capsules of a placebo (specially designed and prepared for the study) at breakfast, lunch and dinner during 8 weeks (Placebo arm).

干预措施: Placebo (Other)

结局指标

主要结局

Weekly concentration of GIP excretion in stool

时间窗: 4 weeks

To determine weekly concentration of GIP excretion in stool (µg/g of GIP) for both patients randomized to AN-PEP or placebo.

Frequency of GIP excretion in stool

时间窗: 4 weeks

To establish the effect of daily administration of AN-PEP compared to placebo in terms of frequency of GIP excretion in stool episodes in 4 weeks.

Weekly concentration of GIP excretion in urine

时间窗: 4 weeks

To determine weekly concentration of GIP excretion in urine (ng/mL) for both patients randomized to AN-PEP or placebo.

Proportion of patients excreting GIP

时间窗: 4 weeks

To establish the proportion of patients excreting GIP above the theoretical threshold for mucosal damage (\>1.6 µg/g of GIP in stool or \>12 ng/mL in urine)

Frequency of GIP excretion in urine

时间窗: 4 weeks

To establish the effect of daily administration of AN-PEP compared to placebo in terms of frequency of GIP excretion in urine epidodes in 4 weeks

次要结局

  • Differences in quality of life scores(4 weeks)
  • Major symptoms(4 weeks)
  • Biochemical effect of AN-PEP vs. placebo(4 weeks)
  • Clinical effect of AN-PEP vs placebo(4 weeks)

研究者

发起方
Dr. C. Bonorino Udaondo Gastroenterology Hospital
申办方类型
Other Gov
责任方
Principal Investigator
主要研究者

Edgardo Smecuol

Principal Investigator

Dr. C. Bonorino Udaondo Gastroenterology Hospital

研究点 (1)

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