IW-3718 Reduces Heartburn Severity in Patients With Refractory Gastroesophageal Reflux Disease in a Randomized Trial.


Journal

Gastroenterology
ISSN: 1528-0012
Titre abrégé: Gastroenterology
Pays: United States
ID NLM: 0374630

Informations de publication

Date de publication:
06 2020
Historique:
received: 28 06 2019
revised: 07 02 2020
accepted: 14 02 2020
pubmed: 25 2 2020
medline: 18 2 2021
entrez: 25 2 2020
Statut: ppublish

Résumé

Refractory gastroesophageal reflux disease (GERD) reduces quality of life and creates significant financial burden on the health care system. Approximately 30% of patients with GERD who receive label-dose proton pump inhibitors (PPIs) still have symptoms. We performed a trial to evaluate the efficacy and safety of IW-3718, a bile acid sequestrant, as an adjunct to PPI therapy. We performed a multicenter, double-blind, placebo-controlled trial, from March 2016 through April 2017, of 280 patients with confirmed GERD. The patients, stratified by esophagitis status, were randomly assigned (1:1:1:1) to groups given placebo or IW-3718 (500, 1000, or 1500 mg) twice daily, with ongoing label-dose PPI. The primary endpoint was percent change from baseline to week 8 in weekly heartburn severity score. We also analyzed percent change from baseline to week 8 in weekly regurgitation frequency score. Mean changes from baseline to week 8 in weekly heartburn severity scores were reductions of 46.0% in the placebo group, 49.0% in the 500 mg group, 55.1% in the 1000 mg group, and 58.0% in the 1500 mg IW-3718 group (dose-response P = .02). The treatment difference was 11.9% between the 1500 mg IW-3718 and placebo groups (P = .04, analysis of covariance). The mean change in weekly regurgitation frequency score from baseline to week 8 in the 1500 mg IW-3718 vs placebo groups was a reduction of 17.5% (95% confidence interval, reductions of 31.4% to 3.6%). The most common adverse event was constipation (in 8.1% of patients receiving IW-3718 and 7.1% of patients receiving placebo). There were no drug-related serious adverse events. In a randomized trial of patients with refractory GERD, adding 1500 mg IW-3718 to label-dose PPIs significantly reduced heartburn symptoms compared with adding placebo. Regurgitation symptoms also decreased. IW-3718 was well tolerated. (ClinicalTrials.gov, Number: NCT02637557).

Sections du résumé

BACKGROUND & AIMS
Refractory gastroesophageal reflux disease (GERD) reduces quality of life and creates significant financial burden on the health care system. Approximately 30% of patients with GERD who receive label-dose proton pump inhibitors (PPIs) still have symptoms. We performed a trial to evaluate the efficacy and safety of IW-3718, a bile acid sequestrant, as an adjunct to PPI therapy.
METHODS
We performed a multicenter, double-blind, placebo-controlled trial, from March 2016 through April 2017, of 280 patients with confirmed GERD. The patients, stratified by esophagitis status, were randomly assigned (1:1:1:1) to groups given placebo or IW-3718 (500, 1000, or 1500 mg) twice daily, with ongoing label-dose PPI. The primary endpoint was percent change from baseline to week 8 in weekly heartburn severity score. We also analyzed percent change from baseline to week 8 in weekly regurgitation frequency score.
RESULTS
Mean changes from baseline to week 8 in weekly heartburn severity scores were reductions of 46.0% in the placebo group, 49.0% in the 500 mg group, 55.1% in the 1000 mg group, and 58.0% in the 1500 mg IW-3718 group (dose-response P = .02). The treatment difference was 11.9% between the 1500 mg IW-3718 and placebo groups (P = .04, analysis of covariance). The mean change in weekly regurgitation frequency score from baseline to week 8 in the 1500 mg IW-3718 vs placebo groups was a reduction of 17.5% (95% confidence interval, reductions of 31.4% to 3.6%). The most common adverse event was constipation (in 8.1% of patients receiving IW-3718 and 7.1% of patients receiving placebo). There were no drug-related serious adverse events.
CONCLUSIONS
In a randomized trial of patients with refractory GERD, adding 1500 mg IW-3718 to label-dose PPIs significantly reduced heartburn symptoms compared with adding placebo. Regurgitation symptoms also decreased. IW-3718 was well tolerated. (ClinicalTrials.gov, Number: NCT02637557).

Identifiants

pubmed: 32092310
pii: S0016-5085(20)30242-0
doi: 10.1053/j.gastro.2020.02.031
pii:
doi:

Substances chimiques

Bile Acids and Salts 0
Delayed-Action Preparations 0
Proton Pump Inhibitors 0
Colesevelam Hydrochloride P4SG24WI5Q

Banques de données

ClinicalTrials.gov
['NCT02637557']

Types de publication

Comparative Study Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2093-2103

Informations de copyright

Copyright © 2020 The Authors. Published by Elsevier Inc. All rights reserved.

Auteurs

Michael F Vaezi (MF)

Vanderbilt University Medical Center, Nashville, Tennessee. Electronic address: Michael.vaezi@vumc.org.

Ronnie Fass (R)

MetroHealth Medical Center and Case Western Reserve University, Cleveland, Ohio.

Nimish Vakil (N)

University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin.

David S Reasner (DS)

Ironwood Pharmaceuticals, Inc, Boston, Massachusetts.

Robert S Mittleman (RS)

Ironwood Pharmaceuticals, Inc, Boston, Massachusetts.

Michael Hall (M)

Ironwood Pharmaceuticals, Inc, Boston, Massachusetts.

James Z Shao (JZ)

Ironwood Pharmaceuticals, Inc, Boston, Massachusetts.

Yan Chen (Y)

Ironwood Pharmaceuticals, Inc, Boston, Massachusetts.

Lara Lane (L)

Ironwood Pharmaceuticals, Inc, Boston, Massachusetts.

Amy M Gates (AM)

Ironwood Pharmaceuticals, Inc, Boston, Massachusetts.

Mark G Currie (MG)

Ironwood Pharmaceuticals, Inc, Boston, Massachusetts.

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