Clinical trial: the incidence of NSAID-associated endoscopic gastric ulcers in patients treated with PN 400 (naproxen plus esomeprazole magnesium) vs. enteric-coated naproxen alone

被引:57
作者
Goldstein, J. L. [1 ]
Hochberg, M. C. [2 ]
Fort, J. G. [3 ]
Zhang, Y. [3 ]
Hwang, C. [4 ]
Sostek, M. [4 ]
机构
[1] Univ Illinois, Dept Med, Chicago, IL 60612 USA
[2] Univ Maryland, Sch Med, Baltimore, MD 21201 USA
[3] POZEN Inc, Chapel Hill, NC USA
[4] AstraZeneca, Wilmington, DE USA
关键词
NONSTEROIDAL ANTIINFLAMMATORY DRUGS; PROTON PUMP INHIBITORS; LOW-DOSE ASPIRIN; DOUBLE-BLIND; HIGH-RISK; DYSPEPSIA ASSESSMENT; ADHERENCE; USERS; PRESCRIPTION; PREVENTION;
D O I
10.1111/j.1365-2036.2010.04378.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
P>Background Gastroprotective co-therapy may reduce the risk of nonsteroidal anti-inflammatory drug (NSAID)-associated gastric ulcers, but adherence is suboptimal. Aim To compare the incidence of gastric ulcers with PN 400 [enteric-coated (EC) naproxen 500 mg and immediate-release esomeprazole 20 mg], or EC naproxen. Methods Two randomized, double-blind, multicentre studies (PN400-301, PN400-302). Patients [stratified by low-dose aspirin (< 325 mg) use] aged >= 50 years or 18-49 years with a history of ulcer, received PN 400 BID (301, n = 218; 302, n = 210) or EC naproxen 500 mg BID (301, n = 216; 302, n = 210) for 6 months. The primary endpoint was the cumulative incidence of endoscopic gastric ulcers. Results The cumulative incidence of gastric ulcers was significantly lower with PN 400 vs. EC naproxen (301: 4.1% vs. 23.1%, P < 0.001; 302: 7.1% vs. 24.3%, P < 0.001). PN 400 was associated with a lower combined incidence of gastric ulcers vs. EC naproxen in low-dose aspirin users (n = 201) (3.0% vs. 28.4%, P < 0.001) and non-users (n = 653) (6.4% vs. 22.2%, P < 0.001). The incidence of, and discontinuations due to, upper gastrointestinal (UGI) AEs was significantly lower with PN 400 relative to EC naproxen (P < 0.01, both studies). Conclusions PN 400 significantly reduces the incidence of gastric ulcers, regardless of low-dose aspirin use, in at-risk patients, and is associated with improved UGI tolerability relative to EC naproxen (ClinicalTrials.gov, NCT00527782).
引用
收藏
页码:401 / 413
页数:13
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