Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | 정혜경 | * |
| dc.date.accessioned | 2019-04-19T16:30:01Z | - |
| dc.date.available | 2019-04-19T16:30:01Z | - |
| dc.date.issued | 2019 | * |
| dc.identifier.issn | 0269-2813 | * |
| dc.identifier.issn | 1365-2036 | * |
| dc.identifier.other | OAK-24572 | * |
| dc.identifier.uri | https://dspace.ewha.ac.kr/handle/2015.oak/249652 | - |
| dc.description.abstract | Background 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. | * |
| dc.language | English | * |
| dc.publisher | WILEY | * |
| dc.title | Randomised phase 3 trial: tegoprazan, a novel potassium-competitive acid blocker, vs. esomeprazole in patients with erosive oesophagitis | * |
| dc.type | Article | * |
| dc.relation.issue | 7 | * |
| dc.relation.volume | 49 | * |
| dc.relation.index | SCIE | * |
| dc.relation.index | SCOPUS | * |
| dc.relation.startpage | 864 | * |
| dc.relation.lastpage | 872 | * |
| dc.relation.journaltitle | ALIMENTARY PHARMACOLOGY & THERAPEUTICS | * |
| dc.identifier.doi | 10.1111/apt.15185 | * |
| dc.identifier.wosid | WOS:000461070100003 | * |
| dc.author.google | Lee, Kwang Jae | * |
| dc.author.google | Son, Byoung Kwan | * |
| dc.author.google | Kim, Gwang Ha | * |
| dc.author.google | Jung, Hye-Kyung | * |
| dc.author.google | Jung, Hwoon-Yong | * |
| dc.author.google | Chung, Il-Kwun | * |
| dc.author.google | Sung, In-Kyung | * |
| dc.author.google | Kim, Jin Il | * |
| dc.author.google | Kim, Jong Hyeok | * |
| dc.author.google | Lee, Joon Seong | * |
| dc.author.google | Kwon, Joong Goo | * |
| dc.author.google | Park, Jung Ho | * |
| dc.author.google | Huh, Kyu Chan | * |
| dc.author.google | Park, Kyung Sik | * |
| dc.author.google | Park, Moo-In | * |
| dc.author.google | Kim, Nayoung | * |
| dc.author.google | Lee, Oh Young | * |
| dc.author.google | Jee, Sam Ryong | * |
| dc.author.google | Lee, Sang Kil | * |
| dc.author.google | Youn, Sei Jin | * |
| dc.author.google | Kim, Sung Kook | * |
| dc.author.google | Lee, Soo Teik | * |
| dc.author.google | Hong, Su Jin | * |
| dc.author.google | Choi, Suck Chei | * |
| dc.author.google | Kim, Tae Nyeun | * |
| dc.author.google | Youn, Young Hoon | * |
| dc.author.google | Park, Hyo Ju | * |
| dc.author.google | Kang, Min Ja | * |
| dc.author.google | Park, Chi Hye | * |
| dc.author.google | Kim, Bong Tae | * |
| dc.author.google | Youn, Sangjun | * |
| dc.author.google | Song, Geun Seog | * |
| dc.author.google | Rhee, Poong-Lyul | * |
| dc.contributor.scopusid | 정혜경(7403029723) | * |
| dc.date.modifydate | 20260618103912 | * |