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Tegoprazan matches PPI healing rates in erosive esophagitis

Erosive esophagitis Erosive esophagitis
Erosive esophagitis Erosive esophagitis

What's new?

Tegoprazan redefines treatment for erosive esophagitis, delivering results on par with PPIs while drawing focus to the evaluation of its long-term safety profile.

A new systematic review and meta-analysis highlights tegoprazan, a novel potassium-competitive acid blocker (P-CAB), as a promising substitute to proton pump inhibitors (PPIs) for erosive esophagitis (EE). The findings come amid growing concerns about the long-term safety of PPIs, which remain the standard therapy for acid-related disorders.

This Preferred Reporting Items for Systematic reviews and Meta-Analyses (PRISMA)-guided study examined 3 randomized controlled trials comprising 658 patients with EE. Primary endpoints focused on endoscopic healing at 4 and 8 weeks, while secondary outcomes captured overall and drug-related treatment-emergent adverse events (TEAEs) as well as serious adverse events (SAEs), providing a precise and thorough appraisal of tegoprazan’s therapeutic impact. Tegoprazan demonstrated non-inferior healing outcomes comparable to PPIs at both 4 and 8 weeks in patients with EE (Table 1).

Overall, adverse events and SAEs showed no statistically significant difference between groups (RR = 1.19, 95% CI : 0.92–1.53; P = 0.19; I² = 24%), while drug-related TEAEs were considerably higher in the tegoprazan group (RR = 1.23, 95% CI: 1.03–1.48; P = 0.02; I2 = 0%). Investigators concluded that tegoprazan delivered healing outcomes comparable to PPIs in EE, while the higher incidence of drug-related adverse events highlighted the need for further investigation into its long-term safety before routine use.

Source:

European Journal of Gastroenterology & Hepatology

Article:

Tegoprazan vs. proton pump inhibitors for erosive esophagitis: a superior alternative or just another option? A systematic review and meta-analysis of randomized controlled trials

Authors:

Muhammad Anas Nayyer et al.

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