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Potassium-competitive acid blocker vs proton-pump inhibitor in patients receiving antithrombotic therapy who are at high risk for gastrointestinal bleeding: Rationale and design of the randomized PROTECT- HBR trial

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Author(s)
Jinho LeeHan-Su ParkJunghoon LeeKee Don ChoiDo-Yoon KangJung-Min AhnWeon KimJong-Young LeeYoung-Hyo LimSe Hun KangSung Uk KwonHanbit ParkEue-Keun ChoiSoon Jun HongByeong-Keuk KimEun-Sun JinJin-Ok JeongChang-Wook NamWang Soo LeeSang Min KimKyoung-Ha ParkSung-Ho HerEun-Seok ShinYoung Jin ChoiTae-Hyun YangSang-Hyun KimJung-Won SuhHwan-Cheol ParkYong-Hoon YoonMyeong-Ho YoonSeung-Jung ParkDuk-Woo Park
Keimyung Author(s)
Nam, Chang Wook
Department
Dept. of Internal Medicine (내과학)
Journal Title
Am Heart J
Issued Date
2025
Volume
287
Abstract
Background:
Concomitant use of proton pump inhibitor (PPI) is recommended in patients receiving chronic antithrombotic therapy who are at high risk of gastrointestinal (GI) bleeding. However, long-term safety and efficacy of chronic PPI use have been concerned. Potassium-competitive acid blocker (P-CAB) is a novel class of acid suppressants, providing more acid stability, rapid onset of action, less variability with CYP2C19 polymorphisms, and longer duration of action than PPI.

Design:
The PROTECT-HBR trial is a multicenter, randomized, double-blind, double-dummy, parallel-group clinical trial. Approximately 3320 patients with known cardiac or vascular disease receiving antithrombotic drugs (either antiplatelet or anticoagulant agents) and who are at high risk of GI bleeding will be randomized to P-CAB (tegoprazan 50mg once daily) or PPI (rabeprazole 20mg once daily) for up to 12 months. The primary endpoint is a composite outcome of upper GI clinical events, including overt or occult GI bleeding, symptomatic gastroduodenal ulcers or erosions, obstruction, or perforation, at 12 months. Secondary endpoints also included cardiovascular events and safety outcomes.

Results:
As of December 2024, approximately 1460 patients were enrolled from 32 participating sites in South Korea. The complete enrollment is anticipated at the mid- or late-term of 2025, and the primary results will be available by 2027.

Conclusion:
PROTECT-HBR is a large-scale, multicenter, clinical trial, which will provide a pivotal comparison of the efficacy and safety of novel P-CAB, tegoprazan with those of PPI, rabeprazole in patients with documented cardiac or vascular disease receiving chronic antithrombotic drugs and at high risk of GI bleeding.

Clinical Trial Registration:
Potassium-Competitive Acid Blocker versus pROton-Pump Inhibitor for GastroproTECTion Strategies In Patients at High GastroIntestinal Bleeding Risk Receiving Antithrombotic Therapy (PROTECT-HBR): NCT04416581.
Keimyung Author(s)(Kor)
남창욱
Publisher
School of Medicine (의과대학)
Type
Article
ISSN
1097-6744
Source
https://www.sciencedirect.com/science/article/pii/S0002870325001061
DOI
10.1016/j.ahj.2025.04.001
URI
https://kumel.medlib.dsmc.or.kr/handle/2015.oak/46339
Appears in Collections:
1. School of Medicine (의과대학) > Dept. of Internal Medicine (내과학)
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