Short-term, temporary insulin degludec, an ultra-long-acting basal insulin, as compared with glargine on the glycemic control in Japanese patients with type 2 diabetes

2013 ◽  
Author(s):  
Shizuka Kaneko ◽  
Yumiko Tahara ◽  
Yuichi Sato ◽  
Masao Tashima
2019 ◽  
Vol 10 (4) ◽  
pp. 1347-1356
Author(s):  
Jakob Langer ◽  
Michael L. Wolden ◽  
Seiya Shimoda ◽  
Miki Sato ◽  
Eiichi Araki

2019 ◽  
Vol 34 (4) ◽  
pp. 382 ◽  
Author(s):  
Han Na Jang ◽  
Ye Seul Yang ◽  
Seong Ok Lee ◽  
Tae Jung Oh ◽  
Bo Kyung Koo ◽  
...  

2020 ◽  
Vol 9 (4) ◽  
pp. 1091
Author(s):  
Sarah J. Glastras ◽  
Neale Cohen ◽  
Thomas Dover ◽  
Gary Kilov ◽  
Richard J. MacIsaac ◽  
...  

Treatment intensification in people with type 2 diabetes following failure of basal insulin commonly involves the addition of a rapid-acting insulin analogue (basal plus one or more prandial doses; multiple daily injections) or by a switch to premixed insulin. Insulin degludec/insulin aspart (IDegAsp), comprising rapid-acting insulin aspart and ultra-long-acting insulin degludec in solution, enables both fasting and post-prandial glucose control, with some advantages over other treatment intensification options. These include straightforward dose titration, flexibility in dose timing, low injection burden, simplicity of switching and a lower risk of hypoglycaemia. In Australia, where insulin degludec on its own is not available, IDegAsp enables patients to still benefit from its ultra-long-acting properties. This review aims to provide guidance on where and how to use IDegAsp. Specifically, guidance is included on the initiation of IDegAsp in insulin-naïve patients, treatment intensification from basal insulin, switching from premixed or basal-bolus insulin to IDegAsp, up-titration from once- to twice-daily IDegAsp and the use of IDegAsp in special populations or situations.


2018 ◽  
Vol 21 ◽  
pp. S128-S129
Author(s):  
J. Langer ◽  
M.L. Wolden ◽  
S. Shimoda ◽  
M. Sato ◽  
E. Araki

2013 ◽  
Vol 09 (01) ◽  
pp. 6 ◽  
Author(s):  
Etie Moghissi ◽  

Due to the progressive nature of Type 2 diabetes, insulin therapy is often required to achieve glycemic control. When lifestyle modifications and treatment with metformin with or without other oral antidiabetic drugs (OADs) have failed to achieve normoglycemia, timely initiation of singledose basal insulin treatment is a convenient, effective, and recommended strategy. The development of the long-acting basal insulin analogs, insulin detemir (IDet) and insulin glargine (IGlar), has resulted in significant improvements in the management of Type 2 diabetes, and specifically, in reducing rates of hypoglycemia. However, hypoglycemia still remains a limiting factor in the intensification of insulin therapy. Combination regimens involving insulin and incretin-based therapies have resulted in improved glycemic control with a similar rate of hypoglycemia compared with insulin alone. Novel basal insulin analogs may also help address the unmet needs associated with basal insulin therapy. Insulin degludec (IDeg) is a basal insulin analog that offers an ultra-long duration of action of more than 42 hours in adults, more flexibility compared with other long-acting insulin analogs in terms of daily dosing times, and reduced rates of hypoglycemia. Pegylated (PEG) lispro, an agent that is currently in clinical development, also offers an extended duration of action. The potential for fewer hypoglycemic episodes offered by combined regimens and new agents may improve adherence to insulin regimens.


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