Medical Division, Novartis Pharma K.K., Tokyo, Japan.
Regulatory Office Japan, Novartis Pharma K.K., Tokyo, Japan.
Expert Opin Pharmacother. 2020 Jan;21(1):121-130. doi: 10.1080/14656566.2019.1685500. Epub 2019 Nov 5.
: Vildagliptin is a dipeptidyl peptidase-4 inhibitor that reduces glycemia in patients with type 2 diabetes mellitus (T2DM). When approved in 2013, data on vildagliptin combined with >750 mg/day metformin in Japanese patients were limited. There is a need to confirm the safety and efficacy of vildagliptin in combination with oral antidiabetic drugs (OADs).: This 52-week post-marketing surveillance (PMS) observational study in Japanese T2DM patients evaluated the safety and efficacy of vildagliptin in combination with OADs including high-dose metformin or insulin but excluding combination with sulfonylureas alone.: During this survey of 3006 Japanese T2DM patients, 13.61% of patients experienced adverse events (AEs) and 2.20% reported a serious AE (SAE). The frequency of AEs/SAEs was similar when in combination with biguanides (12.93%/1.46%), metformin ≥1000 mg/day (12.92%/1.22%), metformin <1000 mg/day (12.62%/1.54%), thiazolidine derivatives (16.71%/2.86%), α-glucosidase inhibitors (13.18%/1.90%), rapid-acting insulin secretagogues (glinides) (20.41%/5.71%), or insulin (15.87%/2.47%). The mean ± SD changes from baseline at endpoint in glycated hemoglobin and fasting blood glucose were -0.76 ± 1.27% and -23.3 ± 57.3 mg/dL, respectively, and these changes were consistent, regardless of concomitant OAD.: Long-term vildagliptin combination therapy is safe and effective in Japanese T2DM patients in real-world settings.
维格列汀是一种二肽基肽酶-4 抑制剂,可降低 2 型糖尿病(T2DM)患者的血糖。2013 年获批时,日本患者中有关维格列汀联合 750 毫克/天以上二甲双胍的数据有限。因此,需要确认维格列汀联合口服降糖药(OAD)的安全性和有效性。
这项在日本 T2DM 患者中开展的 52 周上市后监测(PMS)观察性研究评估了维格列汀联合 OAD(包括高剂量二甲双胍或胰岛素,但不包括与磺酰脲类药物的联合治疗)的安全性和有效性。
在这项对 3006 例日本 T2DM 患者的调查中,13.61%的患者发生了不良事件(AE),2.20%报告了严重不良事件(SAE)。与双胍类药物(12.93%/1.46%)、二甲双胍≥1000mg/天(12.92%/1.22%)、二甲双胍<1000mg/天(12.62%/1.54%)、噻唑烷二酮衍生物(16.71%/2.86%)、α-葡萄糖苷酶抑制剂(13.18%/1.90%)、速效胰岛素分泌剂(格列奈类)(20.41%/5.71%)或胰岛素(15.87%/2.47%)联合治疗时,AE/SAE 的发生频率相似。糖化血红蛋白和空腹血糖自基线至终点的平均变化值分别为-0.76±1.27%和-23.3±57.3mg/dL,这些变化在不同 OAD 联合治疗时是一致的。
在真实世界环境中,长期维格列汀联合治疗对日本 T2DM 患者是安全且有效的。