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Drug Evaluation

An evaluation of canagliflozin for the treatment of type 2 diabetes: an update

, &
Pages 2087-2094 | Received 29 Dec 2020, Accepted 03 Jun 2021, Published online: 11 Jun 2021
 

ABSTRACT

Introduction

Sodium-glucose cotransporter-2 inhibitors (SGLT2is) are proven to ameliorate kidney and heart failure in patients with type 2 diabetes (T2D), in addition to improving glycemic controls. Canagliflozin is a SGLT2i and has proved beneficial for kidney and heart diseases in addition to decreasing the incidence of the composite outcomes of cardiovascular diseases and stroke.

Areas covered

This paper reviews the development of canagliflozin and its effects on renal dysfunction, heart failure, and vascular diseases.

Expert opinion

Canagliflozin contributes to the inhibition of renal function, decline progression and, therefore, is effective for T2D patients with chronic kidney dysfunction and albuminuria. The Canagliflozin Cardiovascular Assessment Study (CANVAS) revealed that patients showed increased incidence of amputation via unknown mechanisms, which has not been observed in other studies that used real-world data. Moreover, canagliflozin has been proven effective for anemia-associated outcomes of chronic kidney failure. Meta-analyses have revealed that canagliflozin contributed to lower diastolic blood pressure when compared with other SGLT2is. A subanalysis of CANVAS data proved that canagliflozin reduced the risk of hemorrhagic stroke. Canagliflozin should be used for T2D patients with chronic kidney failure and/or albuminuria and those with vascular diseases, with monitoring for ulcers and/or the pulse on the lower limb.

Declaration of interest

The author(s) have no relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript. This includes employment, consultancies, honoraria, stock ownership or options, expert testimony, grants or patents received or pending, or royalties.

Reviewer disclosures

One referee declares that they are working on a collaborative project with Taisho Pharma who provided them with luseogliflozin and Tanabe-Mitsubishi who provided canagliflozin. Peer reviewers on this manuscript have no other relevant financial relationships or otherwise to disclose.

Drug summary

Additional information

Funding

This manuscript was not funded.

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