Que Linling, Qin Wei, Shi Yunfei, Ding Ying, Huang Kai, Qian Zhenzhong, Huang Bingjie, Zhou Peipei, He Qing
Drug Clinical Trial Institution, Wuxi People's Hospital Affiliated to Nanjing Medical University, Wuxi, China.
Nanjing Chia-Tai Tianqing Pharmaceutical Company, Nanjing, China.
Front Pharmacol. 2023 Mar 22;14:1105767. doi: 10.3389/fphar.2023.1105767. eCollection 2023.
Janumet XR is the combination of sitagliptin and extended metformin hydrochloride produced by Merck Sharp & Dohme. It is specially designed for diabetes mellitus patients taking both drugs already. Janumet XR exhibited clinically significant blood glucose lowering efficacy and long-term use safety. However, no generic form of Janumet XR has been approved in western countries. The relatively high cost made the medication less prescribed. A more affordable form of this drug may benefit an immense diabetes mellitus population. The current study compared the bioequivalence (BE) of sitagliptin 100 mg and metformin 1000 mg produced by Nanjing Chia-Tai Tianqing Pharmaceutical Company to Janumet XR in healthy Chinese subjects. Twenty-eight healthy Chinese subjects were enrolled in Study 1 and 2, respectively. Both studies were conducted with an open, randomized, two-period crossover design using the test (T) or the reference (R) drug. Study 1 is conducted under the fasting state, and Study 2 is under the fed state. Subjects received an oral dose of sitagliptin 100 mg and metformin 1000 mg, and plasma concentrations of sitagliptin and metformin were determined up to 72 h post-dose. Pharmacokinetic (PK) parameters, including maximum serum concentration (C) and area under the concentration-time curve up to the last quantifiable concentration (AUC) of both sitagliptin and metformin, were calculated and compared between the T and R treatments. In the fasting study, the geometric mean ratios of C, AUC, and AUC for sitagliptin were 109.42%, 101.93%, and 101.95%, respectively; the corresponding ratios for metformin were 98.69%, 94.12%, and 93.42%, respectively. In the fed study, the geometric mean ratios of C, AUC, and AUC for sitagliptin were 98.41%, 100.30%, and 100.24%, respectively; the corresponding ratios for metformin were 97.79%, 99.28%, and 100.69%, respectively. The 90% CIs of C, AUC, and AUC in both studies were all within acceptance limits (80.00%-125.00%). : The results demonstrated for the first time that sitagliptin 100 mg and metformin 1000 mg produced by Nanjing Chia-Tai Tianqing Pharmaceutical Company was bioequivalent to the branded Janumet XR, and both drugs were well tolerated.
捷诺达XR是默克雪兰诺公司生产的西格列汀与缓释盐酸二甲双胍的复方制剂。它是专门为已经在同时服用这两种药物的糖尿病患者设计的。捷诺达XR显示出具有临床意义的降血糖疗效和长期使用安全性。然而,捷诺达XR在西方国家尚未有仿制药获批。相对较高的成本使得该药物的处方量较少。这种药物更实惠的剂型可能会使大量糖尿病患者受益。本研究比较了南京正大天晴制药公司生产的100毫克西格列汀和1000毫克二甲双胍与捷诺达XR在健康中国受试者中的生物等效性(BE)。分别有28名健康中国受试者参加了研究1和研究2。两项研究均采用开放、随机、两周期交叉设计,使用受试(T)或参比(R)药物。研究1在空腹状态下进行,研究2在进食状态下进行。受试者口服100毫克西格列汀和1000毫克二甲双胍,并在给药后72小时内测定西格列汀和二甲双胍的血浆浓度。计算并比较了受试组和参比组治疗中西格列汀和二甲双胍的药代动力学(PK)参数,包括最大血清浓度(C)和至最后可定量浓度的浓度-时间曲线下面积(AUC)。在空腹研究中,西格列汀的C、AUC和AUC的几何平均比值分别为109.42%、101.93%和101.95%;二甲双胍的相应比值分别为98.69%、94.12%和93.42%。在进食研究中,西格列汀的C、AUC和AUC的几何平均比值分别为98.41%、100.30%和100.24%;二甲双胍的相应比值分别为97.79%、99.28%和100.69%。两项研究中C、AUC和AUC的90%置信区间均在可接受范围内(80.00%-125.00%)。结果首次证明,南京正大天晴制药公司生产的100毫克西格列汀和1000毫克二甲双胍与品牌药捷诺达XR生物等效,且两种药物耐受性良好。