Larazotide Acetate for Persistent Symptoms of Celiac Disease Despite a Gluten-Free Diet: A Randomized Controlled Trial

被引:164
作者
Leffler, Daniel A. [1 ]
Kelly, Ciaran P. [1 ]
Green, Peter H. R. [2 ]
Fedorak, Richard N. [3 ]
DiMarino, Anthony [4 ]
Perrow, Wendy [5 ]
Rasmussen, Henrik [5 ]
Wang, Chao [5 ]
Bercik, Premysl [6 ]
Bachir, Natalie M. [7 ]
Murray, Joseph A. [8 ]
机构
[1] Beth Israel Deaconess Med Ctr, Celiac Ctr, Div Gastroenterol, Boston, MA 02215 USA
[2] Columbia Univ, Celiac Dis Ctr, New York, NY USA
[3] Univ Alberta, Ctr Excellence Gastrointestinal Immun & Inflammat, Edmonton, AB, Canada
[4] Thomas Jefferson Univ, Philadelphia, PA 19107 USA
[5] Alba Therapeut Corp, Baltimore, MD USA
[6] McMaster Univ, Hamilton, ON, Canada
[7] Essentia Hlth Duluth Clin, Duluth, MN USA
[8] Mayo Clin, Div Gastroenterol & Hepatol, Rochester, MN 55905 USA
关键词
Celiac Disease; Gluten; Therapeutic; Tight Junction; QUALITY-OF-LIFE; RATING-SCALE; GASTROINTESTINAL SYMPTOMS; INTESTINAL PERMEABILITY; DOUBLE-BLIND; CHALLENGE; LINACLOTIDE; MANAGEMENT; MORTALITY; DIAGNOSIS;
D O I
10.1053/j.gastro.2015.02.008
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
BACKGROUND & AIMS: Celiac disease (CeD) is a prevalent autoimmune condition. Recurrent signs and symptoms are common despite treatment with a gluten-free diet (GFD), yet no approved or proven nondietary treatment is available. METHODS: In this multicenter, randomized, double-blind, placebo-controlled study, we assessed larazotide acetate 0.5, 1, or 2 mg 3 times daily to relieve ongoing symptoms in 342 adults with CeD who had been on a GFD for 12 months or longer and maintained their current GFD during the study. The study included a 4-week placebo run-in, 12 weeks of treatment, and a 4-week placebo run-out phase. The primary end point was the difference in average on-treatment Celiac Disease Gastrointestinal Symptom Rating Scale score. RESULTS: The primary end point was met with the 0.5-mg dose of larazotide acetate, with fewer symptoms compared with placebo by modified intention to treat (n = 340) (analysis of covariance, P = .022; mixed model for repeated measures, P = .005). The 0.5-mg dose showed an effect on exploratory end points including a 26% decrease in celiac disease patient-reported outcome symptomatic days (P = .017), a 31% increase in improved symptom days (P = .034), a 50% or more reduction from baseline of the weekly average abdominal pain score for 6 or more of 12 weeks of treatment (P = .022), and a decrease in the nongastrointestinal symptoms of headache and tiredness (P = .010). The 1- and 2-mg doses were no different than placebo for any end point. Safety was comparable with placebo. CONCLUSIONS: Larazotide acetate 0.5 mg reduced signs and symptoms in CeD patients on a GFD better than a GFD alone. Although results were mixed, this study was a successful trial of a novel therapeutic agent targeting tight junction regulation in patients with CeD who are symptomatic despite a GFD. Clinicaltrials.gov: NCT01396213.
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收藏
页码:1311 / +
页数:15
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