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Evaluation of the Efficacy and Safety of DW1903 in Patients with Gastritis: A Randomized, Double-Blind, Noninferiority, Multicenter, Phase 3 studyopen accessEvaluation of the Efficacy and Safety of DW1903 in Patients with Gastritis: A Randomized, Double-Blind, Noninferiority, Multicenter, Phase 3 study

Authors
Kim, Jie-HyunJung, Hwoon-YongYoo, In KyungPark, Seon-YoungKim, Jae GyuSung, Jae KyuJang, Jin SeokCheon, Gab JinKim, Kyoung OhKim, Tae OhLee, Soo TeikCho, Kwang BumChun, Hoon JaiPark, Jong-JaePark, Moo InJang, Jae-YoungJeon, Seong WooCho, Jin WoongKang, Dae HwanKim, Gwang HaKim, Jae J.Kim, Sang GyunKim, NayoungLee, Yong ChanHong, Su JinKim, Hyun-SooLee, SoraLee, Sang Woo
Issue Date
Jun-2023
Publisher
EDITORIAL OFFICE GUT & LIVER
Keywords
Gastritis; Phase III clinical trial; Proton pump inhibitors; Histamine H2 antagonists
Citation
GUT AND LIVER, v.18, no.1, pp 70 - 76
Pages
7
Journal Title
GUT AND LIVER
Volume
18
Number
1
Start Page
70
End Page
76
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/68007
DOI
10.5009/gnl220446
ISSN
1976-2283
2005-1212
Abstract
Background/Aims: H2 receptor antagonists (H2RA) have been used to treat gastritis by inhibit-ing gastric acid. Proton pump inhibitors (PPIs) are more potent acid suppressants than H2RA. However, the efficacy and safety of low-dose PPI for treating gastritis remain unclear. The aim was to investigate the efficacy and safety of low-dose PPI for treating gastritis.Methods: A double-blind, noninferiority, multicenter, phase 3 clinical trial randomly assigned 476 patients with endoscopic erosive gastritis to a group using esomeprazole 10 mg (DW1903) daily and a group using famotidine 20 mg (DW1903R1) daily for 2 weeks. The full-analysis set in-cluded 319 patients (DW1903, n=159; DW1903R1, n=160) and the per-protocol set included 298 patients (DW1903, n=147; DW1903R1, n=151). The primary endpoint (erosion improvement rate) and secondary endpoint (erosion and edema cure rates, improvement rates of hemorrhage, erythema, and symptoms) were assessed after the treatment. Adverse events were compared.Results: According to the full-analysis set, the erosion improvement rates in the DW1903 and DW1903R1 groups were 59.8% and 58.8%, respectively. According to the per-protocol analysis, the erosion improvement rates in the DW1903 and DW1903R1 groups were 61.9% and 59.6%, respectively. Secondary endpoints were not significantly different between two groups except that the hemorrhagic improvement rate was higher in DW1903 with statistical tendency. The number of adverse events were not statistically different.Conclusions: DW1903 of a low-dose PPI was not inferior to DW1903R1 of H2RA. Thus, low-dose PPI can be a novel option for treating gastritis (ClinicalTrials.gov Identifier: NCT05163756). (Gut Liver, Published online June 13, 2023)
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Kim, Jae Gyu
의과대학 (의학부(임상-서울))
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