Safety and effectiveness of tofogliflozin in Japanese patients with type 2 diabetes mellitus: Results of 24-month interim analysis of a long-term post-marketing study (J-STEP/LT)

被引:8
|
作者
Utsunomiya, Kazunori [1 ]
Kakiuchi, Seigo [2 ]
Senda, Masayuki [3 ]
Fujii, Shoko [2 ]
Kurihara, Yuji [2 ]
Gunji, Ryoji [2 ]
Koshida, Ryusuke [4 ]
Kameda, Hiroyuki [3 ]
Tamura, Masahiro [3 ]
Kaku, Kohei [5 ]
机构
[1] Jikei Univ, Sch Med, Ctr Prevent Med, Tokyo, Japan
[2] Kowa Co Ltd, Post Mkt Surveillance Dept, Tokyo, Japan
[3] Sanofi KK, Post Mkt Clin Res, Tokyo, Japan
[4] Sanofi KK, Med Affairs, Tokyo, Japan
[5] Kawasaki Med Sch, Kurashiki, Okayama, Japan
关键词
Post-marketing study; Sodium-glucose transporter 2; Tofogliflozin; GLUCOSE COTRANSPORTER 2; SGLT2; INHIBITORS;
D O I
10.1111/jdi.13233
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims/Introduction Tofogliflozin is a potent and highly selective sodium-glucose cotransporter 2 inhibitor, and is currently used to treat patients with type 2 diabetes mellitus. We designed a 3-year study of tofogliflozin in patients with type 2 diabetes mellitus to evaluate the safety and effectiveness in routine clinical practice. The 3- and 12-month interim analysis showed tofogliflozin was well-tolerated, safe and clinically effective. Here, we report the results of the 24-month interim analysis. Materials and Methods This is a 3-year prospective, observational and multicenter post-marketing study (Japanese Study of Tofogliflozin with Type 2 Diabetes Mellitus Patients/Long Term). Results Of the 6,897 patients enrolled, 6,712 and 6,461 patients were analyzed for the safety and effectiveness of tofogliflozin, respectively. During the 24-month observation period, the incidence rates of adverse drug reactions (ADRs) and serious adverse drug reactions were 11.25 and 1.21%, respectively. As to adverse drug reactions of special interest, the incidence rates of hypoglycemia, polyuria/pollakiuria, volume depletion-related events, urinary tract infections and genital infection were 0.83, 1.28, 1.46, 1.18 and 1.62%, respectively. Renal disorders, and cardiovascular and cerebrovascular disorders occurred in 0.63 and 0.76% of the patients, respectively. Glycated hemoglobin A1c and bodyweight decreased significantly by -0.70% (P < 0.0001) and -2.95 kg (P < 0.0001), respectively, from baseline to week 104 (last observation carried forward). Conclusions Significant safety concerns have not been observed, and clinical benefit including a long-term reduction in glycated hemoglobin A1c over a 104-week (24 months) observation period with weight loss was suggested in this 24-month interim analysis of the 3-year Japanese Study of Tofogliflozin with Type 2 Diabetes Mellitus Patients/Long Term in routine clinical practice.
引用
收藏
页码:906 / 916
页数:11
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