Effect of Renal Impairment on the Pharmacokinetics and Pharmacodynamics of Tofogliflozin (A SELECTIVE SGLT2 Inhibitor) in Patients with Type 2 Diabetes Mellitus.


Journal

Drug research
ISSN: 2194-9387
Titre abrégé: Drug Res (Stuttg)
Pays: Germany
ID NLM: 101602406

Informations de publication

Date de publication:
Jun 2019
Historique:
pubmed: 14 8 2018
medline: 4 12 2019
entrez: 14 8 2018
Statut: ppublish

Résumé

Tofogliflozin is an orally available selective inhibitor of sodium-glucose co-transporter 2 for treatment of type 2 diabetes mellitus (T2DM). Two studies were conducted to evaluate the effect of renal impairment on pharmacokinetics and pharmacodynamics of tofogliflozin. The studies were: 1) single dose study in T2DM patients with normal renal function and mild, moderate and severe renal impairment, and 2) multiple dose study for 24 weeks in T2DM patients with normal renal function and moderate renal impairment. Renal function did not have a clinically relevant effect on the PK of tofogliflozin. Urinary glucose excretion up to 24 h after administration of tofogliflozin (UGE24h) decreased with decreasing glomerular filtration rate. Lowering UGE24h resulted in waning glycemic control but not body weight reduction. Single and multiple administrations of tofogliflozin were generally well tolerated in T2DM patients with various renal functions. As far as investigated here, these studies indicate no dose adjustment is required for patients with renal impairment.

Identifiants

pubmed: 30103216
doi: 10.1055/a-0662-0209
doi:

Substances chimiques

Benzhydryl Compounds 0
Blood Glucose 0
Glucosides 0
Sodium-Glucose Transporter 2 Inhibitors 0
6-((4-ethylphenyl)methyl)-3',4',5',6'-tetrahydro-6'-(hydroxymethyl)spiro(isobenzofuran-1(3H),2'-(2H)pyran)-3',4',5'-triol P8DD8KX4O4

Types de publication

Clinical Trial, Phase I Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

314-322

Informations de copyright

© Georg Thieme Verlag KG Stuttgart · New York.

Déclaration de conflit d'intérêts

Y.T., N.K., T.S. and S.Iida and S.Ikeda are employees of Chugai Pharmaceutical Co., Ltd. D.S., and A.P. are employees of H. Hoffmann La Roche Co., Ltd.

Auteurs

Sachiya Ikeda (S)

Primary lifecycle Management Department, Chugai Pharmaceutical Co., Ltd., Tokyo, Japan.

Yasuki Takano (Y)

Clinical Science and Strategy Department, Chugai Pharmaceutical Co., Ltd., Tokyo, Japan.

Dietmar Schwab (D)

Pharmaceutical Sciences, Clinical Pharmacology, Roche Pharma Research and Early Development, Roche Innovation Center Basel, Basel, Switzerland.

Agnes Portron (A)

Pharmaceutical Sciences, Clinical Pharmacology, Roche Pharma Research and Early Development, Roche Innovation Center Basel, Basel, Switzerland.

Nahoko Kasahara-Ito (N)

Translational Clinical Research, Clinical Pharmacology Department, Chugai Pharmaceutical Co., Ltd., Tokyo, Japan.

Tomohisa Saito (T)

Translational Clinical Research, Clinical Pharmacology Department, Chugai Pharmaceutical Co., Ltd., Tokyo, Japan.

Satofumi Iida (S)

Translational Clinical Research, Clinical Pharmacology Department, Chugai Pharmaceutical Co., Ltd., Tokyo, Japan.

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Classifications MeSH