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Randomised phase 3 trial: tegoprazan, a novel potassium-competitive acid blocker, vs. esomeprazole in patients with erosive oesophagitis

DC Field Value Language
dc.contributor.authorLee, KJ-
dc.contributor.authorSon, BK-
dc.contributor.authorKim, GH-
dc.contributor.authorJung, HK-
dc.contributor.authorJung, HY-
dc.contributor.authorChung, IK-
dc.contributor.authorSung, IK-
dc.contributor.authorKim, JI-
dc.contributor.authorKim, JH-
dc.contributor.authorLee, JS-
dc.contributor.authorKwon, JG-
dc.contributor.authorPark, JH-
dc.contributor.authorHuh, KC-
dc.contributor.authorPark, KS-
dc.contributor.authorPark, MI-
dc.contributor.authorKim, N-
dc.contributor.authorLee, OY-
dc.contributor.authorJee, SR-
dc.contributor.authorLee, SK-
dc.contributor.authorYoun, SJ-
dc.contributor.authorKim, SK-
dc.contributor.authorLee, ST-
dc.contributor.authorHong, SJ-
dc.contributor.authorChoi, SC-
dc.contributor.authorKim, TN-
dc.contributor.authorYoun, YH-
dc.contributor.authorPark, HJ-
dc.contributor.authorKang, MJ-
dc.contributor.authorPark, CH-
dc.contributor.authorKim, BT-
dc.contributor.authorYoun, S-
dc.contributor.authorSong, GS-
dc.contributor.authorRhee, PL-
dc.date.accessioned2020-10-21T07:21:14Z-
dc.date.available2020-10-21T07:21:14Z-
dc.date.issued2019-
dc.identifier.issn0269-2813-
dc.identifier.urihttp://repository.ajou.ac.kr/handle/201003/18883-
dc.description.abstractBACKGROUND: Tegoprazan is a novel potassium-competitive acid blocker that has a fast onset of action and can control gastric pH for a prolonged period, which could offer clinical benefit in acid-related disorders.
AIM: To confirm the non-inferiority of tegoprazan to esomeprazole in patients with erosive oesophagitis (EE).
METHODS: In this multicentre, randomised, double-blind, parallel-group comparison study, 302 Korean patients with endoscopically confirmed EE (Los Angeles Classification Grades A-D) were randomly allocated to either tegoprazan (50 or 100 mg) or esomeprazole (40 mg) treatment groups for 4 or 8 weeks. The primary endpoint was the cumulative proportion of patients with healed EE confirmed by endoscopy up to 8 weeks from treatment initiation. Symptoms, safety and tolerability were also assessed.
RESULTS: The cumulative healing rates at week 8 were 98.9% (91/92), 98.9% (90/91) and 98.9% (87/88) for tegoprazan 50 mg, tegoprazan 100 mg and esomeprazole 40 mg, respectively. Both doses of tegoprazan were non-inferior to esomeprazole 40 mg. The incidence of adverse events was comparable among the groups, and tegoprazan was well-tolerated.
CONCLUSION: Once daily administration of tegoprazan 50 or 100 mg showed non-inferior efficacy in healing EE and tolerability to that of esomeprazole 40 mg.
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dc.language.isoen-
dc.subject.MESHAdult-
dc.subject.MESHAged-
dc.subject.MESHAnti-Ulcer Agents-
dc.subject.MESHBenzene Derivatives-
dc.subject.MESHDouble-Blind Method-
dc.subject.MESHEsomeprazole-
dc.subject.MESHEsophagitis-
dc.subject.MESHFemale-
dc.subject.MESHHumans-
dc.subject.MESHImidazoles-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHPotassium-
dc.subject.MESHProton Pump Inhibitors-
dc.subject.MESHTreatment Outcome-
dc.subject.MESHWound Healing-
dc.subject.MESHYoung Adult-
dc.titleRandomised phase 3 trial: tegoprazan, a novel potassium-competitive acid blocker, vs. esomeprazole in patients with erosive oesophagitis-
dc.typeArticle-
dc.identifier.pmid30843245-
dc.identifier.urlhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6594096/-
dc.contributor.affiliatedAuthor이, 광재-
dc.type.localJournal Papers-
dc.identifier.doi10.1111/apt.15185-
dc.citation.titleAlimentary pharmacology & therapeutics-
dc.citation.volume49-
dc.citation.number7-
dc.citation.date2019-
dc.citation.startPage864-
dc.citation.endPage872-
dc.identifier.bibliographicCitationAlimentary pharmacology & therapeutics, 49(7). : 864-872, 2019-
dc.identifier.eissn1365-2036-
dc.relation.journalidJ002692813-
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Gastroenterology
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