scholarly journals Antiperistaltic effect and safety of l ‐menthol oral solution on gastric mucosa for upper gastrointestinal endoscopy in Chinese patients: Phase III, multicenter, randomized, double‐blind, placebo‐controlled study

2021 ◽  
Author(s):  
Fandong Meng ◽  
Wenyan Li ◽  
Fachao Zhi ◽  
Zhaoshen Li ◽  
Zhanxiong Xue ◽  
...  
2021 ◽  
Author(s):  
Richard B Lipton ◽  
Sagar Munjal ◽  
Stewart J Tepper ◽  
Charles Iaconangelo ◽  
Daniel Serrano

Abstract Background Safe, effective, oral therapies are needed for acute treatment of migraine. This clinical trial assessed the efficacy, tolerability, and safety of celecoxib oral solution (ELYXYB) in a single migraine attack associated with moderate-to-severe pain. Methods This Phase III, randomized, double-blind, placebo-controlled, multicenter trial treated adults with episodic migraine (with or without aura) with a single 4.8 mL dose of 120-mg celecoxib oral solution or placebo. Co-primary endpoints were the proportion of patients who were pain-free and free from the most bothersome migraine symptom (MBS) at 2 hours post-dose. The MBS was identified at screening from among nausea, photophobia, or phonophobia. Results Six hundred thirty-one patients were randomized (mean age 41 years, range 18–75; 84.3% female). One study site met prespecified outlier criteria and was excluded from efficacy analyses. This site had a mean 2-hour pain freedom placebo response rate of 75% vs 23.5% for all other sites. In subsequent analysis, 2-hour post-dose pain freedom response rates were significantly higher in the celecoxib oral solution group vs placebo (32.8%, [27.2%, 38.8%]) vs 23.5%, [18.5%, 29.2%]; P = 0.020). For 2-hour post-dose MBS freedom, response rates were significantly higher in the celecoxib oral solution group vs placebo (58.1% [51.4%, 64.5%] vs 43.9% [37.2%, 50.7%]; P = 0.003). A total of 10.7% (31/289) of patients treated with celecoxib oral solution and 9.9% (28/283) of placebo-treated patients reported a treatment-emergent adverse event (TEAE). Study drug-related TEAEs were reported by 7.3% (21/289) and 7.4% (21/283) of celecoxib oral solution and placebo patients, respectively; the most common were nausea (celecoxib oral solution: 1.4% [4/289] vs placebo: 1.8% [5/283]) and dysgeusia (celecoxib oral solution: 1.7% [5/289] vs placebo: 1.1% [3/283]). No serious TEAEs, deaths, or drug-related TEAEs leading to withdrawal were reported. Conclusions Celecoxib oral solution is a safe, effective COX-2-selective nonsteroidal anti-inflammatory drug for the treatment of acute migraine. In this analysis, celecoxib oral solution was significantly more effective than placebo and was also associated with a low rate of gastric TEAEs. Celecoxib oral solution may provide a convenient, alternate option to currently available treatments. Trial registration: ClinicalTrials.gov Identifier: NCT03009019; Registered January 4, 2017; Retrospectively registered, https://clinicaltrials.gov/ct2/show/NCT03009019


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