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Tegoprazan: A Next-Generation P-CAB Redefining Acid Suppression

Dr. R. Jona Methusala, Thouday Keerthi*

Zenodo (CERN European Organization for Nuclear Research), 2025

Abstract

Tegoprazan is a novel, potent, and highly selective potassium-competitive acid blocker that inhibits gastric and secretion with rapid onset of action and prolonged control of gastric acidity. In patients with gastroesophageal reflux disease (GERD)whose symptoms improve with acid-suppression therapy, on-demand treatment could constitute maintenance therapy. Potassium-competitive acid blockers and proton pump inhibitors/sodium bicarbonate can rapidly increase intragastric pH. A novel and varied class of medications known as potassium-competitive acid blockers (P-CABs), like tegoprazan, can totally block the potassium-binding site of gastric H+/K+ ATPase, potentially getting around the restrictions of proton-pump inhibitors (PPIs). This mechanism allows for consistent acid suppression across a wide pH range and minimizes variability due to CYP2C19 polymorphisms or food intake. Clinical trials have demonstrated tegoprazan’s efficacy in managing gastroesophageal reflux disease (GERD), peptic ulcers, and Helicobacter pylori infection. It achieves rapid symptoms relief and high healing rates, with a favorable safety profile and minimal adverse effects. Pharmacokinetic reveal a peak plasma concentration within 1-2hours and a half-life of approximately 7-10hours, supporting once-daily dosing. Pharmacodynamic data confirm sustained intragastric pH elevation, even during night time periods. This review consolidates current evidence on tegoprazan’s pharmacology, clinical applications,…

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