Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Atsushi Utsuno"'
Autor:
Eiji Ueyama, Satoshi Yoshida, H. Ishikawa, Hideyuki Takahashi, Kenichi Kazuta, Atsunori Kashiwagi, Atsushi Utsuno
Publikováno v:
Diabetes, Obesity and Metabolism. 17:152-160
Aims To assess the effects of renal impairment (RI) on the efficacy and safety of ipragliflozin in patients with type 2 diabetes mellitus (T2DM). Methods A cohort of Japanese patients with T2DM and mild to moderate RI and poor glycaemic control, desp
Autor:
Atsunori Kashiwagi, Eiji Ueyama, Kenichi Kazuta, Noriko Akiyama, Satoshi Yoshida, Takanori Shiga, Atsushi Utsuno
Publikováno v:
Diabetology International. 6:125-138
Sulfonylureas are often used alone or in combination with other drugs for treating type 2 diabetes. Ipragliflozin is a sodium/glucose cotransporter 2 inhibitor that enhances urinary glucose excretion and improves glycemic control. We examined the eff
Autor:
Noriko Akiyama, Atsunori Kashiwagi, Atsushi Utsuno, Kenichi Kazuta, Eiji Ueyama, Satoshi Yoshida, Takanori Shiga
Publikováno v:
Diabetology International. 6:104-116
Ipragliflozin is a novel oral sodium–glucose cotransporter 2 (SGLT2) inhibitor under development for the treatment of type 2 diabetes. We examined its efficacy and safety as an add-on to pioglitazone in Japanese patients with inadequately controlle
Publikováno v:
Diabetes, Obesity & Metabolism
This multicenter, double-blind, placebo-controlled study examined the efficacy and safety of ipragliflozin, a sodium-glucose co-transporter 2 inhibitor, in combination with metformin in Japanese patients with type 2 diabetes mellitus (T2DM). Patients
Autor:
Atsushi Utsuno, Shigeru Kageyama, Shigenori Kawasaki, Takeshi Kadokura, Itsuro Nagase, Satoshi Yoshida, Masako Saito, Kenichi Kazuta
Publikováno v:
Diabetology International. 2:172-182
This phase 1, randomized, placebo-controlled, dose-escalation study evaluated the safety, tolerability, pharmacokinetics, and pharmacodynamics of ipragliflozin (ASP1941) in healthy Japanese subjects. Subjects received a single oral dose (1–300 mg)
Autor:
Shigeru Kageyama, Satoshi Yoshida, Itsuro Nagase, Atsushi Utsuno, Ronald A. Smulders, Noriko Akiyama, Atsunori Kashiwagi, Kenichi Kazuta, Takeshi Kadokura
Publikováno v:
Diabetes research and clinical practice. 106(1)
Aims Ipragliflozin is a novel and highly selective sodium–glucose transporter 2 (SGLT2) inhibitor that reduces plasma glucose levels by enhancing urinary glucose excretion in patients with type 2 diabetes mellitus (T2DM). We examined the pharmacoki
Publikováno v:
Carbohydrate Research. 207:71-79
O-alpha-D-Glucopyranosyl-(1----6)-O-beta-D-glucopyranosyl-(1----6)-1-N- [L-aspart-1-oyl-(L-proline)-4-oyl]-alpha- and -beta-D-glucopyranosylamine have been prepared, as models for a derivative possibly present in the glomerular basement membrane of r