Real-World Safety of Vonoprazan in Patients and Symptom Outcomes in Patients With Reflux Esophagitis in China: A Prospective, Non-Interventional Study (VIEW)

Ying Lian Xiao , Hui Yang , Yi Xia Lu , Li Yang , Guo Xin Zhang , Guo Liang Ye , Qi Song , Li Xie , Min Hu Chen

Journal of Digestive Diseases ›› 2026, Vol. 27 ›› Issue (3-4) : 150 -159.

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Journal of Digestive Diseases ›› 2026, Vol. 27 ›› Issue (3-4) :150 -159. DOI: 10.1111/1751-2980.70051
ORIGINAL ARTICLE
Real-World Safety of Vonoprazan in Patients and Symptom Outcomes in Patients With Reflux Esophagitis in China: A Prospective, Non-Interventional Study (VIEW)
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Abstract

Objectives: Vonoprazan was approved in China for reflux esophagitis (RE) in 2019; however, its real-world safety and effectiveness remain undetermined. We aimed to evaluate the safety of vonoprazan in patients and its effectiveness in patients with RE in a real-world setting.

Methods: In this prospective, non-interventional, real-world study, vonoprazan 20 mg was administered orally daily for 4 or 8 weeks. Primary endpoints were incidence rates of adverse events (AEs), serious AEs (SAEs), and adverse drug reactions (ADRs). Secondary endpoints included proportions of patients with RE without typical gastroesophageal reflux disease (GERD) symptoms (complete symptom relief) at baseline and Week 4, relief of heartburn/regurgitation symptoms (all day/nighttime) during Week 1, and mean change in GERD Questionnaire (GERDQ) score at Week 4.

Results: Of the 2829 patients with safety data, 488 (17.2%) reported ≥ 1 AE; 29 (1.0%) reported ≥ 1 SAE; and 129 (4.6%) reported ≥ 1 ADR. Of 1796 patients with RE and effectiveness data, the proportion without typical symptoms of GERD increased from 20.1% (95% confidence interval [CI] 18.29–22.05) at baseline to 55.2% (95% CI 52.63–57.79) at Week 4 (change: 35.1%, 95% CI 31.95–38.25). Complete relief from heartburn, nighttime heartburn, regurgitation, and nighttime regurgitation was observed in 32.3% (314/971), 43.8% (427/975), 27.0% (262/971), and 40.5% (395/976) patients, respectively, during Week 1. Mean change in GERDQ score (n = 1464) improved by Week 4 (−1.70).

Conclusion: Vonoprazan is well tolerated through 8 weeks in patients and improves symptoms in patients with RE in the real-world setting in China (VIEW; NCT04501627).

Keywords

esophagitis, peptic / gastroesophageal reflux disease / potassium competitive acid blockers / vonoprazan

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Ying Lian Xiao, Hui Yang, Yi Xia Lu, Li Yang, Guo Xin Zhang, Guo Liang Ye, Qi Song, Li Xie, Min Hu Chen. Real-World Safety of Vonoprazan in Patients and Symptom Outcomes in Patients With Reflux Esophagitis in China: A Prospective, Non-Interventional Study (VIEW). Journal of Digestive Diseases, 2026, 27 (3-4) : 150-159 DOI:10.1111/1751-2980.70051

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2026 The Author(s). Journal of Digestive Diseases published by Chinese Medical Association Shanghai Branch, Chinese Society of Gastroenterology, Renji Hospital Affiliated to Shanghai Jiaotong University School of Medicine and John Wiley & Sons Australia, Ltd.

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