Influence of Demographic Factors on Clinical Outcomes in Adults With Chronic Idiopathic Constipation Treated With Plecanatide

被引:2
作者
Rao, Satish S. C. [1 ]
Laitman, Adam P. [2 ]
Miner, Philip B., Jr. [3 ]
机构
[1] Augusta Univ, Digest Hlth Ctr, Div Gastroenterol & Hepatol, Augusta, GA 30912 USA
[2] Salix Pharmaceut, Bridgewater, NJ USA
[3] Oklahoma Fdn Digest Res, Oklahoma City, OK USA
关键词
bowel movement; constipation; demographics; guanylate cyclase-C agonist; plecanatide; TRIAL;
D O I
10.14309/ctg.0000000000000598
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
INTRODUCTION: Chronic idiopathic constipation (CIC) is a common condition that affects some patient groups more often. Demographic/clinical characteristics can differ in presentation and therapeutic response. The impact of these characteristics on plecanatide efficacy/safety was examined. METHODS: Data from 2 identically designed, randomized, phase 3 trials of adults with CIC receiving 3 mg of plecanatide, 6 mg of plecanatide, or placebo for 12 weeks were analyzed. Subgroups were baseline age, body mass index (BMI), race/ethnicity, and sex/gender. Endpoints included durable overall complete spontaneous bowel movement (CSBM) responder rate, weekly CSBMs and spontaneous bowel movements (SBMs), and adverse events. RESULTS: Overall (N = 2,639; 3mgof plecanatide [n = 877]; 6mg of plecanatide [n = 877]; and placebo [n = 885]), CSBM responder rates were significantly greater with 3 mg of plecanatide and 6 mg of plecanatide vs placebo in subgroups with those younger than 65 years (P < 0.001), females (P < 0.001), White individuals (P < 0.001), and BMI <25 kg/m(2) (P <= 0.004) and 25-30 kg/m(2) (P < 0.001); as well, for 3 mg: 65 years or older (P = 0.03), non-White individuals (P < 0.001), and BMI >= 30 kg/m(2) (P = 0.02). Improvement from baseline in weekly CSBM and SBM frequency occurred in all subgroups for both plecanatide doses vs placebo (P <= 0.02) at week 12, except those aged 65 years or older for 6 mg of plecanatide. The most common adverse event was diarrhea (3 mg [4.9%]; 6 mg [5.4%]; and placebo [1.3%]). DISCUSSION: Pooled data from identically designed CIC trials strengthened the ability to identify meaningful subgroup comparisons regarding plecanatide efficacy and safety.
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