Department of Family Practice and Community Health, Ajou University School of Medicine, Suwon, Republic of Korea.
CTCBIO Inc., Hwaseong, Republic of Korea.
Clin Pharmacol Drug Dev. 2018 Jan;7(1):53-58. doi: 10.1002/cpdd.331. Epub 2017 Jan 23.
CDFR0209, a combination of an immediate-release formulation of omeprazole 40 mg and sodium bicarbonate 1100 mg, has been developed to treat acid-related disorders. We compared the acid inhibitory effects of CDFR0209 and delayed-release omeprazole (omeprazole-DR, Losec 40 mg) after repeated dosing in Helicobacter pylori-negative healthy adult male subjects. In this 2-period crossover study, 30 subjects were randomized to CDFR0209 or omeprazole-DR daily for 7 days. An ambulatory continuous 24-hour intragastric pH recording was performed at baseline and on days 1 and 7 of each administration period. Integrated gastric acidity was calculated from time-weighted average hydrogen ion concentrations at each hour of the 24-hour record. An analysis of variance model was used to test the pharmacodynamic equivalence of CDFR0209 and omeprazole-DR, using the natural logarithmic transformation of the percent decrease from baseline in integrated gastric acidity for the 24-hour interval after the seventh dose of each omeprazole formulation. The geometric least-squares mean ratios (CDFR0209/omeprazole-DR) of the percent decrease from baseline in integrated gastric acidity was 0.98 (90%CI, 0.93-1.07). Both CDFR0209 and omeprazole-DR are equally effective in decreasing integrated gastric acidity at steady state.
CDFR0209 是一种奥美拉唑 40mg 速释制剂和碳酸氢钠 1100mg 的复方制剂,用于治疗与胃酸相关的疾病。我们比较了 CDFR0209 和延迟释放奥美拉唑(omeprazole-DR,Losec 40mg)在幽门螺杆菌阴性健康成年男性受试者中重复给药后的抑酸效果。在这项 2 期交叉研究中,30 名受试者被随机分为 CDFR0209 或 omeprazole-DR 组,每天给药 7 天。在基线和每个给药期的第 1 天和第 7 天进行了 24 小时动态连续胃内 pH 记录。通过 24 小时记录中每小时的时加权平均氢离子浓度计算总体酸度。使用每个奥美拉唑制剂第 7 次给药后 24 小时间隔内,总体酸度相对于基线的对数转换后,从方差分析模型检验 CDFR0209 和 omeprazole-DR 的药效等效性。CDFR0209/omeprazole-DR 的几何均数比值(%)为 0.98(90%CI,0.93-1.07)。在稳态时,CDFR0209 和 omeprazole-DR 均能有效降低总体酸度。