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DOI 10.1016/j.ahj.2025.04.001

Медицинская библиотека · American heart journal · 2025

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.

Lee Jinho, Park Han-Su, Lee Junghoon, Choi Kee Don, Kang Do-Yoon, Ahn Jung-Min, Kim Weon, Lee Jong-Young, Lim Young-Hyo, Kang Se Hun, Kwon Sung Uk, Park Hanbit, Choi Eue-Keun, Hong Soon Jun, Kim Byeong-Keuk, Jin Eun-Sun, Jeong Jin-Ok, Nam Chang-Wook, Lee Wang Soo, Kim Sang Min, Park Kyoung-Ha, Her Sung-Ho, Shin Eun-Seok, Choi Young Jin, Yang Tae-Hyun, Kim Sang-Hyun, Suh Jung-Won, Park Hwan-Cheol, Yoon Yong-Hoon, Yoon Myeong-Ho, Park Seung-Jung, Park Duk-Woo, PROTECT-HBR Trial

Протокол клинического исследованияСтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

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.

Для цитирования: Lee Jinho, Park Han-Su, Lee Junghoon, Choi Kee Don, Kang Do-Yoon, Ahn Jung-Min, Kim Weon, Lee Jong-Young, Lim Young-Hyo, Kang Se Hun, Kwon Sung Uk, Park Hanbit, Choi Eue-Keun, Hong Soon Jun, Kim Byeong-Keuk, Jin Eun-Sun, Jeong Jin-Ok, Nam Chang-Wook, Lee Wang Soo, Kim Sang Min, Park Kyoung-Ha, Her Sung-Ho, Shin Eun-Seok, Choi Young Jin, Yang Tae-Hyun, Kim Sang-Hyun, Suh Jung-Won, Park Hwan-Cheol, Yoon Yong-Hoon, Yoon Myeong-Ho, Park Seung-Jung, Park Duk-Woo, PROTECT-HBR Trial. 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.. American heart journal. 2025. DOI: 10.1016/j.ahj.2025.04.001.

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